Phytoecdysteroids and Anabolic Effect of Atriplex dimorphostegia: UPLC-PDA-MS/MS Profiling, In Silico and In Vivo Models
Open accessAbstract
Atriplex dimorphostegia (Saltbush) is an annual halophytic shrub that is widely distributed across various parts of Asia. The current study is the first to report the metabolites profile of the total ethanol extract of the aerial parts of A. dimorphostegia (TEAD), and its anabolic activity together with the isolated 20-hydroxyecdysone (20-HE) in orchidectomized male rats. TEAD was analyzed and standardized utilizing UPLC-PDA-ESI–MS/MS and UPLC-PDA-UV techniques, resulting in tentative identification of fifty compounds including polyphenols, steroids and triterpenoids. In addition, 20-HE was quantified, representing 26.79 μg/mg of the extract. Phytochemical investigation of TEAD resulted in the isolation of 20-HE from the ethyl acetate fraction (EFAD) and was identified by conventional spectroscopic methods of analysis. Furthermore, the anabolic effect of the isolated 20-HE and TEAD was then evaluated using in silico and in vivo models. Molecular docking experiments revealed in vitro selectivity of 20-HE towards estrogen receptors (ERs), specifically ERβ over ERα and androgenic receptor (AR). The anabolic efficacy of TEAD and 20-HE was studied in orchidectomized immature male Wistar rats using the weight of gastrocnemius and soleus muscles. The weights of ventral prostate and seminal vesicles were used as indicators for androgenic activity. Rats administered 20-HE and TEAD showed a significant increase (p = 0.0006 and p < 0.0001) in the net muscle mass compared to the negative control, while the group receiving TEAD showed the highest percentage among all groups at p < 0.0001. Histopathological investigation of skeletal muscle fibers showed normal morphological structures, and the group administered 20-HE showed an increase in cross sectional area of muscle fibers comparable to methandienone and testosterone groups at p > 0.99. A. dimorphostegia exhibited promising anabolic activity with minimal androgenic side effects.
AI snapshot
Written from the paper’s full text.
TL;DR
The first metabolic profiling of *Atriplex dimorphostegia* aerial-parts ethanol extract tentatively identified 50 compounds and quantified 20-hydroxyecdysone at 26.79 µg/mg. In orchidectomized male rats, TEAD and 20-HE increased muscle mass with low androgenic effects, while docking suggested 20-HE selectively binds ERβ over ERα and AR.
Key findings
- UPLC-PDA-ESI-MS/MS tentatively identified 50 compounds, including polyphenols, phenolic acids, flavonoids, phytosterols, triterpenoids, and steroids; 20-HE was quantified at 26.79 ± 0.57 µg/mg of TEAD.
- In orchidectomized immature male Wistar rats, 20-HE and TEAD increased net muscle mass versus negative control by 76% and 112% (p = 0.0006 and p < 0.0001); TEAD showed the highest muscle mass percentage (0.64%), two-fold the negative control.
- Testosterone increased prostate and seminal vesicle mass 14-fold versus negative control and 17-fold versus 20-HE/TEAD groups (p < 0.0001); methandienone had the highest anabolic ratios (27.92 and 8.79), while TEAD was not significantly different from methandienone (p > 0.99).
- Docking indicated 20-HE binds ERβ similarly to estradiol, with steric clashes in ERα and AR binding sites suggesting ERβ selectivity; 20-HE and TEAD showed IC50 > 100 µg/mL in human skeletal muscle cells.
Methods
- Plant material was extracted by maceration in absolute ethanol, fractionated with n-hexane then ethyl acetate, and 20-HE was isolated from the ethyl acetate fraction and identified by NMR and LC-ESI-MS; TEAD was profiled and standardized by UPLC-PDA-ESI-MS/MS and UPLC-PDA-UV.
- In silico docking used PDB structures 3OLL, 3UUD, and 2AM9 for ERβ, ERα, and AR with AutoDock Vina in Chimera; validation RMSD values were 0.508, 0.643, and 0.751.
- In vivo: 25 immature male Wistar rats were orchidectomized, 23 were randomized into five groups, and treated for 10 days with vehicle, methandienone (5 mg/kg), testosterone enanthate (0.1 mg/kg), 20-HE (5 mg/kg), or TEAD (185 mg/kg); muscle bundle, sex organs, histology, cross-sectional area, and fiber number were assessed using ANOVA with Tukey–Kramer post hoc tests.
Limitations
- The paper states that future studies are needed on the pharmacokinetics of TEAD and 20-HE in rats, as well as lifespan, biodistribution, and muscle tissue retention, and that further clinical investigation is warranted.
- Evident from the text: the in vivo study was small (23 rats) and short-term (10 days), used only orchidectomized immature male rats, and did not include female or intact animals.
- Evident from the text: metabolite identification was tentative by UPLC-MS/MS, and the selectivity conclusion relies on docking rather than direct receptor-binding assays.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 34 cited sources checked · 0 supported · 0 flagged
- Findingown data
TEAD contains 20-hydroxyecdysone (20-HE) at 26.79 ± 0.57 μg per mg of extract.
“Each mg of TEAD was shown to contain 26.79 ± 0.57 µg of 20-HE.”
Quote in the paperSubstantial claim - Findingown data
The docked pose of 20-HE in the ERβ binding site is similar to that of the co-crystallized ligand estradiol.
“The docked pose of 20-HE in the binding site of ERβ reveals a binding mode similar to that of the co-crystallized ligand, estradiol.”
Quote in the paperSubstantial claim - Findingown data
Administration of 20-HE increased net muscle mass in orchidectomized male rats compared to the negative control by 76% (p = 0.0006).
“Similarly, the administration of 20-HE and TEAD increased the net mass of muscles significantly (p = 0.0006 and p < 0.0001) compared to the negative control by 76% and 112%, respectively.”
Quote in the paperSubstantial claim - Findingcitation
The molecular formula of the isolated 20-HE is C27H44O7.
“A molecular formula of C27H44O7 related to 20-HE was then deduced and confirmed according to the literature [36,37,38,39].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [36] Nguir, 2015, New Septanoside and 20-Hydroxyecdysone Septanoside Derivative from Atriplex portulacoides Roots with Preliminary Biological Activities, Bioorg. Med. Chem. Lett. source
Not checked in the free run.
- cites [37] Olennikov, 2018, Makisterone C-20,22-Acetonide from Rhaponticum uniflorum, Chem. Nat. Compd. source
Not checked in the free run.
- cites [38] Yusupova, 2022, Phytochemical Constituents and Biological Activities of Dianthus helenae Vved., Growing in Uzbekistan, Nat. Prod. Res.
Not checked in the free run.
- cites [39] Girault, 1988, The Complete 1H-NMR Assignment of Ecdysone and 20-Hydroxyecdysone, J. Insect Physiol. source
Not checked in the free run.
- Findingown data
There was no significant difference in net muscle mass between the 20-HE and TEAD groups (p > 0.5).
“There was no significant (p > 0.5) difference between 20-HE and TEAD (Figure 8).”
Quote in the paperSubstantial claim
- Findingcitation
The purity of the isolated 20-HE was 99.5% by HPLC.
“The purity of the compound was elucidated by HPLC and was found to be 99.5% [35].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [35] Mani, 2017, Purification and Structural Elucidation of Three Bioactive Compounds Isolated from Streptomyces coelicoflavus BC 01 and Their Biological Activity, 3 Biotech.
Not checked in the free run.
- Findingown data
20-HE and TEAD did not affect the viability of human skeletal muscle cells at concentrations up to 100 μg/mL (IC50 > 100 μg/mL).
“20-HE and TEAD exhibited no effect on cell viability at concentrations equal to or greater than 0.01 µg/mL with an IC50 of > 100 µg/mL.”
Quote in the paperSubstantial claim - Findingown data
Administration of TEAD increased net muscle mass in orchidectomized male rats compared to the negative control by 112% (p < 0.0001).
“Similarly, the administration of 20-HE and TEAD increased the net mass of muscles significantly (p = 0.0006 and p < 0.0001) compared to the negative control by 76% and 112%, respectively.”
Quote in the paperSubstantial claim - Findingown data
There was no significant difference in the number of muscle fibers between the 20-HE and TEAD groups (p = 0.6).
“There was no significant difference (p = 0.6) between the groups receiving 20-HE and TEAD.”
Quote in the paperNot a substantial claim - Findingown data
TEAD treatment resulted in muscle fiber size (683 ± 86 μm2) significantly different from testosterone (p < 0.0001) and methandienone (p = 0.0004).
“However, TEAD treatment (683 ± 86 µm²) showed significant difference when compared to testosterone (p < 0.0001) and methandienone (p = 0.0004).”
Quote in the paperSubstantial claim - Findingown data
There was no significant difference in muscle fiber size between methandienone (946 ± 132 μm2) and 20-HE (p > 0.99).
“Similarly, no significant difference (p > 0.99) when comparing methandienone (946 ± 132 µm²) to 20-HE treatments.”
Quote in the paperSubstantial claim - Findingown data
The number of muscle fibers increased in all groups compared to the negative control (p < 0.0001).
“The number of muscle fibers increased in all groups when compared to the negative control at p < 0.0001 (Figure 15).”
Quote in the paperSubstantial claim - Findingown data
Muscle fiber cross-sectional area increased in all groups compared to the negative control (p < 0.0001).
“The size of muscles increased (p < 0.0001) in all groups compared to the negative control (Figure 14).”
Quote in the paperSubstantial claim - Findingown data
Testosterone increased prostate and seminal vesicle mass by 14-fold compared to the negative control (p < 0.0001).
“Group C receiving testosterone showed a significant (p < 0.0001) increase in the mass of prostate and seminal vesicles, a 14-fold increase in comparison with the negative control.”
Quote in the paperSubstantial claim - Findingown data
Testosterone increased prostate and seminal vesicle mass by 17-fold compared to the 20-HE and TEAD groups (p < 0.0001).
“Moreover, when comparing group C to groups receiving 20-HE and TEAD, the mass of prostate and seminal vesicles also increased significantly (p < 0.0001), by 17-folds (Figure 9).”
Quote in the paperSubstantial claim - Findingown data
Administration of A. dimorphostegia total ethanol extract increased the cross-sectional area of muscle fibers in rats.
“This was represented by the increase in net muscle mass of gastrocnemius and soleus muscle, as well as an increase in the cross-sectional area of muscle fibers.”
Quote in the paperSubstantial claim - Findingown data
20-HE and TEAD did not increase the weights of prostate and seminal vesicles in rats after ten consecutive days of administration.
“both 20-HE and TEAD exhibited a low androgenic effect on sex organs without increasing the weights of prostate and seminal vesicles of rats after administration for ten consecutive days.”
Quote in the paperSubstantial claim - Findingown data
Administration of A. dimorphostegia total ethanol extract increased net muscle mass of gastrocnemius and soleus muscles in rats.
“This was represented by the increase in net muscle mass of gastrocnemius and soleus muscle, as well as an increase in the cross-sectional area of muscle fibers.”
Quote in the paperSubstantial claim - Premisecitation
Ecdysteroids do not bind to androgenic receptors (ARs).
“When compared to AAS, ecdysteroids do not bind to androgenic receptors (ARs).”
Quote in the paperSubstantial claim0 of 2 sources checked - Premisecitation
Ecdysteroids have shown anabolic effects in vertebrates and humans.
“Interestingly, ecdysteroids, a class of hormones found in arthropods responsible for molting and reproduction, have shown anabolic effects in vertebrates and humans [5,6,7].”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [5] Hirunsai, 2016, Effect of 20-Hydroxyecdysone on Proteolytic Regulation in Skeletal Muscle Atrophy, In Vivo source
Not checked in the free run.
- cites [6] Parr, 2015, Ecdysteroids: A Novel Class of Anabolic Agents?, Biol. Sport source
Not checked in the free run.
- cites [7] Isenmann, 2019, Ecdysteroids as Non-Conventional Anabolic Agent: Performance Enhancement by Ecdysterone Supplementation in Humans, Arch. Toxicol. source
Not checked in the free run.
- Study design and conductcitation
The anabolic efficacy of TEAD and isolated 20-HE was evaluated using testosterone enanthate and methandienone as positive controls in orchidectomized immature male Wistar rats.
“The anabolic efficacy of TEAD and the isolated 20-HE was evaluated using testosterone enanthate and methandienone as positive controls in orchidectomized immature male Wistar rats [6].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [6] Parr, 2015, Ecdysteroids: A Novel Class of Anabolic Agents?, Biol. Sport source
Not checked in the free run.
- Premisecitation
20-HE has well-documented anabolic potency.
“a phytoecdysteroid that was proven to have low acute toxicity [8] and an anabolic potency that have been well documented [6,7,19,76].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [6] Parr, 2015, Ecdysteroids: A Novel Class of Anabolic Agents?, Biol. Sport source
Not checked in the free run.
- cites [7] Isenmann, 2019, Ecdysteroids as Non-Conventional Anabolic Agent: Performance Enhancement by Ecdysterone Supplementation in Humans, Arch. Toxicol. source
Not checked in the free run.
- cites [19] Kacsala, 2008, 20-Hydroxyecdysone Increases Fiber Size in a Muscle-Specific Fashion in Rat, Phytomedicine source
Not checked in the free run.
- cites [76] Chermnykh, 1988, The Action of Methandrostenolone and Ecdysterone on the Physical Endurance of Animals and on Protein Metabolism in the Skeletal Muscles, Farm. Toksikol.
Not checked in the free run.
- Premisenone given
The current study is the first to report these compounds in A. dimorphostegia.
“However, the current study is the first to report these compounds in A. dimorphostegia.”
Quote in the paperSubstantial claim- Rests on an assumption: No literature reports the metabolic profile of A. dimorphostegia aerial parts responsible for its anabolic potential.
- Study design and conductown data
The docking protocol was valid.
“To validate the docking protocol, the co-crystallized ligands were re-docked using the same docking parameters. The generated docking poses were identical to the co-crystallized poses for ERβ, ERα and AR with RMSD values of 0.508, 0.643 and 0.751, respectively. This indicates a valid docking protocol.”
Quote in the paperSubstantial claim - Interpretationown data
The Atriplex dimorphostegia total ethanol extract has anabolic potency.
“The Atriplex dimorphostegia total ethanol extract proved anabolic potency.”
Quote in the paperSubstantial claim - Interpretationown data
20-HE and TEAD exhibited a low androgenic effect on sex organs in rats.
“both 20-HE and TEAD exhibited a low androgenic effect on sex organs without increasing the weights of prostate and seminal vesicles of rats after administration for ten consecutive days.”
Quote in the paperSubstantial claim - Interpretationreasoning
A. dimorphostegia is a promising candidate for use as an anabolic agent.
“These findings indicate that A. dimorphostegia is a promising candidate for use as an anabolic agent and warrants further clinical investigation.”
Quote in the paperSubstantial claim- Rests on an assumption: Findings of anabolic effects in orchidectomized rats are predictive of anabolic effects in humans.
- The quote only partly states this claim. 1
- May combine two claims. 17
- Classified as probably not a substantial claim. 10
The quote only partly states this claim.
Findingown data20-HE exhibits in silico selectivity towards estrogen receptors (ERs), specifically ERβ over ERα and the androgenic receptor (AR).
“Molecular docking experiments revealed in vitro selectivity of 20-HE towards estrogen receptors (ERs), specifically ERβ over ERα and androgenic receptor (AR).”
Quote in the paperNot a substantial claimMay combine two claims.
FindingcitationFifty compounds were tentatively identified in TEAD, including phenolic acids and their derivatives, flavonoids and their derivatives, phytosterols, triterpenoids and steroids.
“Fifty compounds were tentatively identified, including phenolic acids and their derivatives, flavonoids, and their derivatives [41]. In addition, phytosterols, triterpenoids and steroids were also identified.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [41] Ayoub, N., Badr, N., Al-Ghamdi, S.S., Alsanosi, S., Alzahrani, A.R., Abdel-Naim, A.B., Nematallah, K.A., and Swilam, N. (2022). Hplc/Msn Profiling and Healing Activity of a Muco-Adhesive Formula of Salvadora persica against Acetic Acid-Induced Oral Ulcer in Rats. Nutrients, 14. source
Not checked in the free run.
May combine two claims.
Findingcitation20-HE was isolated from the ethyl acetate fraction (EFAD) of A. dimorphostegia and identified as a white crystalline solid (55 mg, mp 237.5-239.5 °C).
“Phytochemical investigation of the EFAD led to the isolation and identification of 20-HE as a white crystalline solid (Figure 1) (55 mg, mp. 237.5–239.5 °C) [34].”
Quote in the paperSubstantial claim0 of 1 sources checked- cites [34] Argay, 2002, Crystal Structures of Ecdysteroids: The Role of Solvent Molecules in Hydrogen Bonding and Isostructurality, Acta Cryst. B source
Not checked in the free run.
May combine two claims.
Findingown dataThe muscle bundle to prostate and seminal vesicles ratio in the TEAD group was significantly different from the negative control (p = 0.002) and testosterone (p < 0.0001).
“The muscle bundle to prostate and seminal vesicles ratio showed a significant difference in the group receiving TEAD when compared to the negative control and testosterone groups at p values of 0.002 and <0.0001 respectively.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataTestosterone treatment produced the maximum increase in muscle fiber size (1017 ± 100 μm2), with no significant difference compared to 20-HE (941 ± 168 μm2) (p = 0.67).
“While testosterone treatment showed a maximum increase in muscle fiber size (1017 ± 100 µm²), there was no significant (p = 0.67) difference when compared to 20-HE (941 ± 168 µm²).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe testosterone group had the lowest anabolic to androgenic ratios (1.01 and 1.07), significantly different from the methandienone group (p < 0.0001 and 0.0005).
“The group receiving testosterone showed the lowest ratios (1.01 and 1.07), significantly different from the methandienone group at p values of <0.0001 and 0.0005, respectively.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThere was no significant difference in the muscle bundle to prostate and seminal vesicles ratio between TEAD and methandienone (p > 0.99) or between TEAD and 20-HE (p > 0.99).
“There is no significant (p > 0.99) difference between the group receiving TEAD when compared to methandienone, and neither is there a significant difference when compared to 20-HE (p > 0.99).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe 20-HE group did not differ significantly from the negative control in the muscle bundle to prostate and seminal vesicles ratio, but differed significantly from testosterone (p = 0.0036).
“When comparing the group receiving 20-HE compared to the negative control, the difference is not significant, but the difference compared to testosterone is significant at p = 0.0036.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe methandienone group had the highest number of muscle fibers (49.5 ± 4.5), significantly higher than the 20-HE and TEAD groups (p < 0.0001).
“The group receiving methandienone showed the highest number of muscle fibers (49.5 ± 4.5), significantly higher than the groups receiving 20-HE and TEAD at p < 0.0001.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataHistopathological examination showed almost normal morphological structures of skeletal muscle fibers, without abnormal subcellular alterations, inflammatory infiltrates, or vascular abnormalities.
“All samples stained with H&E demonstrated almost normal morphological structures of skeletal muscle fibers, without abnormal subcellular alterations with normal intact intermuscular fine connective tissue, without abnormal inflammatory cell infiltrates and with normal vasculatures (Figure 13).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe methandienone group had the highest anabolic to androgenic ratios (27.92 and 8.79), significantly different from the negative control (p = 0.001 and 0.01).
“The group receiving methandienone had the highest anabolic ratios (27.92 and 8.79), showing a significant difference when compared to the negative control at p values of 0.001 and 0.01, respectively.”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe TEAD group showed the highest muscle mass percentage (0.64%) among all groups, two-fold compared to the negative control.
“The group receiving TEAD showed the highest percentage (0.64%) among all groups, two-fold compared to the negative control.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataSteric clashes negatively influence the binding stability of 20-HE in the binding sites of ERα and AR, and indirectly improve its selectivity towards ERβ.
“The docked poses of 20-HE revealed that the steric clashes negatively influence the binding stability of 20-HE in the binding sites of ERα and AR, and indirectly improve selectivity towards ERβ.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataA. dimorphostegia exhibited promising anabolic activity with minimal androgenic side effects.
“A. dimorphostegia exhibited promising anabolic activity with minimal androgenic side effects.”
Quote in the paperSubstantial claimMay combine two claims.
InterpretationcitationTEAD is a potential anabolic agent containing 20-HE together with other secondary metabolites previously reported to have anabolic effects and activities that promote muscle health.
“It could be concluded that TEAD is a potential anabolic agent containing 20-HE together with other secondary metabolites which previously reported to have anabolic effects and activities that promote muscle health [7,73,74,75,76,77,78].”
Quote in the paperSubstantial claim0 of 7 sources checked- cites [7] Isenmann, 2019, Ecdysteroids as Non-Conventional Anabolic Agent: Performance Enhancement by Ecdysterone Supplementation in Humans, Arch. Toxicol. source
Not checked in the free run.
- cites [73] Hamed, 2014, el Chemo-protective effect on hepato-renal toxcicity and cytotoxic activity of lipoidal matter of atriplex lindleyi moq, Orig. Artic. Artic. Int. J. Pharm. Pharm. Sci.
Not checked in the free run.
- cites [74] Rozenberg, 2003, Phytosterol Analysis and Characterization in Spelt (Triticum aestivum Ssp. Spelta L.) and Wheat (T. Aestivum L.) Lipids by LC/APCI-MS, J. Cereal Sci. source
Not checked in the free run.
- cites [75] Chen, 2011, Identification and Quantification of Oleanolic Acid and Ursolic Acid in Chinese Herbs by Liquid Chromatography-Ion Trap Mass Spectrometry, Biomed. Chromatogr. source
Not checked in the free run.
- cites [76] Chermnykh, 1988, The Action of Methandrostenolone and Ecdysterone on the Physical Endurance of Animals and on Protein Metabolism in the Skeletal Muscles, Farm. Toksikol.
Not checked in the free run.
- cites [77] Wang, 2020, Antioxidant Apigenin Relieves Age-Related Muscle Atrophy by Inhibiting Oxidative Stress and Hyperactive Mitophagy and Apoptosis in Skeletal Muscle of Mice, J. Gerontol. -Ser. A Biol. Sci. Med. Sci. source
Not checked in the free run.
- cites [78] Jang, 2017, Apigenin Enhances Skeletal Muscle Hypertrophy and Myoblast Differentiation by Regulating Prmt7, Oncotarget source
Not checked in the free run.
May combine two claims.
Study design and conductown dataA calibration curve for 20-HE was established with the equation y = 0.1248x + 1.1292 and a correlation coefficient R2 = 0.9892.
“The calibration curve equation was established as y = 0.1248x + 1.1292 with a correlation coefficient of R² = 0.9892 (Figure 2b).”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductreasoningMolecular docking used PDB entries 3OLL, 3UUD and 2AM9 for ERβ, ERα and AR, respectively, selected as ligand-bound crystal structures to allow ligand docking into the ligand-binding site.
“In these experiments, the protein data bank (PDB) entries 3OLL, 3UUD and 2AM9 were used for ERβ, ERα and AR, respectively [84,85,86]. These crystal structures were specifically selected as they are in ligand-bound states and therefore their conformations would allow ligand docking into the ligand-binding site.”
Quote in the paperSubstantial claim0 of 3 sources checked- cites [84] Cantin, 2006, Comparison of Crystal Structures of Human Androgen Receptor Ligand-Binding Domain Complexed with Various Agonists Reveals Molecular Determinants Responsible for Binding Affinity, Protein Sci. source
Not checked in the free run.
- cites [85] Rose, 2010, Synthesis and Crystal Structure of a Phosphorylated Estrogen Receptor Ligand Binding Domain, ChemBioChem source
Not checked in the free run.
- cites [86] Delfosse, 2012, Structural and Mechanistic Insights into Bisphenols Action Provide Guidelines for Risk Assessment and Discovery of Bisphenol A Substitutes, Proc. Natl. Acad. Sci. USA source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationSelective activation of ERβ potently induces regeneration and fibrogenesis in toxin-injured muscle in female rats.
“Accumulating evidence showed that selective activation of ERβ potently induces regeneration and fibrogenesis in toxin-injured muscle in female rats [15].”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites [15] Velders, 2012, Selective Estrogen Receptor-β Activation Stimulates Skeletal Muscle Growth and Regeneration, FASEB J. source
Not checked in the free run.
May combine two claims.
Premisenone givenThe current study is the first to report the metabolites profile of the total ethanol extract of the aerial parts of A. dimorphostegia (TEAD) and its anabolic activity together with isolated 20-HE in orchidectomized male rats.
“The current study is the first to report the metabolites profile of the total ethanol extract of the aerial parts of A. dimorphostegia (TEAD), and its anabolic activity together with the isolated 20-hydroxyecdysone (20-HE) in orchidectomized male rats.”
Quote in the paperSubstantial claim- Rests on an assumption: No literature reports the metabolic profile of A. dimorphostegia aerial parts responsible for its anabolic potential.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenThe plant material was identified by Prof. Dr. Ahmed K. Othman, Biology Department, Faculty of Science, Northern Border University, Saudi Arabia.
“The plant collected was identified by Prof. Dr. Ahmed K. Othman, Biology Department, Faculty of Science, Northern Border University, Saudi Arabia.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenA voucher specimen (PHG-P-AM-245) was deposited at the herbarium of the Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, Egypt.
“A voucher specimen was placed at the herbarium (PHG-P-AM-245) at the Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, Egypt.”
Quote in the paperNot a substantial claimMay combine two claims.
PremisecitationBoth ERα and ERβ are expressed in skeletal muscles of mice and humans.
“Both ERα and ERβ are expressed in skeletal muscles of mice and humans [10,12,13,14].”
Quote in the paperSubstantial claim0 of 4 sources checked- cites [10] Wiik, 2009, Expression of Both Oestrogen Receptor Alpha and Beta in Human Skeletal Muscle Tissue, Histochem. Cell Biol. source
Not checked in the free run.
- cites [12] Milanesi, 2009, Expression and Subcellular Distribution of Native Estrogen Receptor β in Murine C2C12 Cells and Skeletal Muscle Tissue, Steroids source
Not checked in the free run.
- cites [13] Wiik, 2003, Oestrogen Receptor β Is Expressed in Adult Human Skeletal Muscle Both at the MRNA and Protein Level, Acta Physiol. Scand. source
Not checked in the free run.
- cites [14] Milanesi, 2008, Expression and Localization of Estrogen Receptor α in the C2C12 Murine Skeletal Muscle Cell Line, J. Cell Biochem. source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Premisecitation20-HE has low acute toxicity.
“the most widely investigated ecdysteroid was 20-HE due to its low acute toxicity [8,19].”
Quote in the paperNot a substantial claim0 of 2 sources checked- cites [8] Bathori, 2008, Phytoecdysteroids and Anabolic-Androgenic Steroids - Structure and Effects on Humans, Curr. Med. Chem. source
Not checked in the free run.
- cites [19] Kacsala, 2008, 20-Hydroxyecdysone Increases Fiber Size in a Muscle-Specific Fashion in Rat, Phytomedicine source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataTwo rats died at days 2 and 5 after orchidectomy.
“Rats were then left to recover for one week; two rats died at days 2 and 5.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataTwenty-three rats were randomly divided into five groups.
“Twenty-three rats with an average weight of 62.25 ± 10.26 g were randomly divided into five groups and treated with test compounds by gavage and subcutaneous (SC) injection (Figure 16).”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenThree independent experiments with three internal replicates were performed in the SRB-U assay.
“Three independent experiments with three internal replicates were performed.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataAnimal handling and experimental design were approved by the Research Ethics Committee of the Faculty of Pharmacy, British University in Egypt.
“Handling of animals and experimental design were approved and conducted according to the guidelines of the Research Ethics Committee of the Faculty of Pharmacy, British University in Egypt, Cairo. (Approval No. EX-2217).”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductnone givenNine random non-overlapping fields per sample tissue section were analyzed for determination of muscle fiber cross-sectional area.
“Nine random non-overlapping fields per sample tissue section were analyzed for determination of muscle fibers cross sectional area.”
Quote in the paperSubstantial claim
The paper relies on this without support.
No literature reports the metabolic profile of A. dimorphostegia aerial parts responsible for its anabolic potential.
“Considering the cited studies, nothing was found in the literature reporting the metabolic profile of A. dimorphostegia aerial parts responsible for its anabolic potential.”
The paper relies on this without support.
Findings of anabolic effects in orchidectomized rats are predictive of anabolic effects in humans.
“These findings indicate that A. dimorphostegia is a promising candidate for use as an anabolic agent and warrants further clinical investigation.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Phytoecdysteroids influence signal transduction through membrane-bound receptors, particularly estrogen receptors (alpha and beta).
“Phytoecdysteroids influence signal transduction through membrane-bound receptors, particularly estrogen receptors (alpha and beta) [65,66].”
From Phytoecdysteroids: Quantification in Selected Plant Species and Evaluation of Some Effects on Gastric Smooth Muscles (2024) · cites this paper as [66]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
Chromatography stages exceed the stated run time
MinorThe listed stages last 35, 15, 15, 15 and 10 minutes, totaling 90 minutes rather than the stated 70 minutes.
Reported 70 · recomputed 90
“The separation was performed for a total of 70 min using gradient elution from 10% to 75% B in A for the first 35 min at a flow rate 0.5 mL/min”
Compound 27 fragment does not match the stated loss
MinorSubtracting the stated 308-unit loss from the precursor at m/z 579.2 gives 271.2, not the reported fragment at m/z 345.
Reported 345 · recomputed 271.2
“Compound 27 was identified as syringetin rutinoside with a molecular ion peak [M−H]− at m/z 579.2 and a fragment ion peak at m/z 345 owing to the loss of the rutinoside moiety [M−H−(308)]−”
Cites
UCSF Chimera—A visualization system for exploratory research and analysis
Pettersen, E. F., Goddard, T. D., Huang, C. C., Couch, G. S., Greenblatt, D. M., Meng, E. C., & Ferrin, T. E. (2004) · Journal of Computational Chemistry · doi:10.1002/jcc.20084 · Cited by 45,260 · see citing works
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196 · see citing works
Trott, O., & Olson, A. J. (2010) · Journal of Computational Chemistry · doi:10.1002/jcc.21334 · Cited by 38,412 · see citing works
New Colorimetric Cytotoxicity Assay for Anticancer-Drug Screening
Skehan, P., Storeng, R., Scudiero, D. A., Monks, A. P., McMahon, J., Vistica, D. T., Warren, J. T., Bokesch, H. R., Kenney, S., & Boyd, M. R. (1990) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/82.13.1107 · Cited by 9,801 · see citing works
Abubakar, A., & Haque, M. (2020) · Journal of Pharmacy And Bioallied Sciences · doi:10.4103/jpbs.jpbs_175_19 · Cited by 1,629 · see citing works
Delfosse, V., Grimaldi, M., Pons, J.-L., Boulahtouf, A., le Maire, A., Cavailles, V., Labesse, G., Bourguet, W., & Balaguer, P. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1203574109 · Cited by 405 · see citing works
Brito, A., Ramirez, J., Areche, C., Sepúlveda, B., & Simirgiotis, M. J. (2014) · Molecules · doi:10.3390/molecules191117400 · Cited by 358 · see citing works
Kunkel, S. D., Suneja, M., Ebert, S. M., Bongers, K. S., Fox, D. K., Malmberg, S. E., Alipour, F., Shields, R. K., & Adams, C. M. (2011) · Cell Metabolism · doi:10.1016/j.cmet.2011.03.020 · Cited by 345 · see citing works
Molecular Mechanisms of Estrogen Action: Selective Ligands and Receptor Pharmacology
Katzenellenbogen, B. S., Choi, I., Delage-Mourroux, R., Ediger, T. R., Martini, P. G. V., Montano, M., Sun, J., Weis, K., & Katzenellenbogen, J. A. (2000) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/s0960-0760(00)00104-7 · Cited by 289 · see citing works
Pereira de Jésus‐Tran, K., Côté, P., Cantin, L., Blanchet, J., Labrie, F., & Breton, R. (2006) · Protein Science · doi:10.1110/ps.051905906 · Cited by 278 · see citing works
Estrogen receptor and aryl hydrocarbon receptor signaling pathways
Matthews, J. B., & Gustafsson, J.-Α. (2006) · Nuclear Receptor Signaling · doi:10.1621/nrs.04016 · Cited by 277 · see citing works
Allam, R. M., Al-Abd, A. M., Khedr, A., Sharaf, O. A., Nofal, S. M., Khalifa, A. E., Mosli, H. A. M., & Abdel‐Naim, A. B. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.04.008 · Cited by 262 · see citing works
Anabolic-Androgenic Steroid Therapy in the Treatment of Chronic Diseases
Basaria, S. S., Wahlstrom, J. T., & Dobs, A. S. (2001) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.86.11.7983 · Cited by 242 · see citing works
Chen, H.-J., Inbaraj, B. S., & Chen, B. (2011) · International Journal of Molecular Sciences · doi:10.3390/ijms13010260 · Cited by 224 · see citing works
Barros, L., Dueñas, M., Días, M. I., Sousa, M. J., Santos‐Buelga, C., & Ferreira, I. C. F. R. (2012) · Food Chemistry · doi:10.1016/j.foodchem.2012.07.107 · Cited by 221 · see citing works
Phytoecdysteroids and Anabolic Androgenic Steroids--Structure and Effects on Humans
Bathori, M., Toth, N., Hunyadi, A., Marki, A., & Zador, E. (2008) · Current Medicinal Chemistry · doi:10.2174/092986708783330674 · Cited by 201 · see citing works
Christou, M. A., Christou, P. A., Markozannes, G., Tsatsoulis, A., Mastorakos, G., & Tigas, S. (2017) · Sports Medicine · doi:10.1007/s40279-017-0709-z · Cited by 199 · see citing works
Said, R. B., Hamed, A. I., Mahalel, U. A., Al-Ayed, A. S., Kowalczyk, M., Mołdoch, J., Oleszek, W. A., & Stochmal, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18030512 · Cited by 196 · see citing works
Expression of Both Oestrogen Receptor Alpha and Beta in Human Skeletal Muscle Tissue
Wiik, A., Ekman, M., Johansson, O., Jansson, E., & Esbjörnsson, M. (2009) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0512-x · Cited by 190 · see citing works
Ibrahim, R. M., Halawany, A. M. E., Saleh, D. O., Naggar, E. M. B. E., El-Shabrawy, A.-R., & El‐Hawary, S. S. (2015) · Revista Brasileira de Farmacognosia · doi:10.1016/j.bjp.2015.02.008 · Cited by 175 · see citing works
Phytoecdysteroids increase protein synthesis in skeletal muscle cells.
Gorelick-Feldman, J., MacLean, D., Ilic, N., Poulev, A., Lila, M. A., Cheng, D., & Raskin, I. (2008) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf073059z · Cited by 166 · see citing works
Selective estrogen receptor-β activation stimulates skeletal muscle growth and regeneration
Velders, M., Schleipen, B., Fritzemeier, K. H., Zierau, O., & Diel, P. (2012) · The FASEB Journal · doi:10.1096/fj.11-194779 · Cited by 162 · see citing works
Bystrom, L. M., Lewis, B. A., Brown, D. L., ., E. R., & Obendorf, R. L. (2008) · Food Chemistry · doi:10.1016/j.foodchem.2008.04.058 · Cited by 155 · see citing works
Polyphenols profile of pomegranate leaves and their role in green synthesis of silver nanoparticles
Swilam, N., & Nematallah, K. A. (2020) · Scientific Reports · doi:10.1038/s41598-020-71847-5 · Cited by 154 · see citing works
Self-citationSimirgiotis, M. J., Benites, J. F., Areche, C., & Sepúlveda, B. (2015) · Molecules · doi:10.3390/molecules200611490 · Cited by 146 · see citing works
Guo, H. J., Liu, A., Ye, M., Yang, M., & Guo, D. (2007) · Rapid Communications in Mass Spectrometry · doi:10.1002/rcm.2875 · Cited by 142 · see citing works
Atriplex halimus L.: Its biology and uses
Walker, D. J., Lutts, S., Sánchez‐García, M., & Corréal, E. (2013) · Journal of Arid Environments · doi:10.1016/j.jaridenv.2013.09.004 · Cited by 128 · see citing works
Isenmann, E., Ambrosio, G., Joseph, J. F., Mazzarino, M., de la Torre, X., Zimmer, P., Kazlauskas, R., Goebel, C., Botrè, F., Diel, P., et al. (2019) · Archives of Toxicology · doi:10.1007/s00204-019-02490-x · Cited by 127 · cited 2× · see citing works
“A significant increase in muscle mass was observed without an increase in biomarkers for liver or kidney toxicity [7].”
BackgroundAnabolic steroids abuse and male infertility
Osta, R. E., Almont, T., Diligent, C., Hubert, N., Eschwège, P., & Hubert, J. (2016) · Basic and Clinical Andrology · doi:10.1186/s12610-016-0029-4 · Cited by 127 · see citing works
Antioxidant activity of methanolic extracts and some bioactive compounds of Atriplex halimus
Benhammou, N., Bekkara, F. A., & Panovska, T. K. (2009) · Comptes Rendus Chimie · doi:10.1016/j.crci.2009.02.004 · Cited by 124 · see citing works
Wiik, A., Glenmark, B., Ekman, M., Esbjörnsson‐Liljedahl, M., Johansson, O., Bodin, K., Enmark, E., & Jansson, E. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.0001-6772.2003.01186.x · Cited by 122 · see citing works
Beelders, T., de Beer, D., Stander, M. A., & Joubert, E. (2014) · Molecules · doi:10.3390/molecules190811760 · Cited by 116 · see citing works
Francescato, L. N., Debenedetti, S. L., Schwanz, T. G., Bassani, V. L., & Henriques, A. T. (2012) · Talanta · doi:10.1016/j.talanta.2012.11.072 · Cited by 111 · see citing works
Characterization of flavonoids in Millettia nitida var. hirsutissima by HPLC/DAD/ESI-MS
Ye, M., Yang, W., Liu, K., Qiao, X., Li, B.-J., Cheng, J. H., Feng, J., Guo, D., & Zhao, Y. (2011) · Journal of Pharmaceutical Analysis · doi:10.1016/j.jpha.2011.09.009 · Cited by 99 · see citing works
Ecdysteroids: A novel class of anabolic agents?
Parr, M., Botrè, F., Naß, A., Hengevoss, J., Diel, P., & Wolber, G. (2014) · Biology of Sport · doi:10.5604/20831862.1144420 · Cited by 95 · cited 4× · see citing works
“An effect even exceeding methandienone was found in vitro [6], and Chermnykh et al.”
BackgroundResultInfluentialRozenberg, R., Ruibal-Mendieta, N. L., Petitjean, G., Cani, P., Delacroix, D. L., Delzenne, N. M., Meurens, M., Quetin-Leclercq, J., & Habib-Jiwan, J.-L. (2003) · Journal of Cereal Science · doi:10.1016/s0733-5210(03)00022-5 · Cited by 94 · see citing works
Synthesis and Crystal Structure of a Phosphorylated Estrogen Receptor Ligand Binding Domain
Möcklinghoff, S., Rose, R., Carraz, M., Visser, A., Ottmann, C., & Brunsveld, L. (2010) · ChemBioChem · doi:10.1002/cbic.201000532 · Cited by 87 · see citing works
Wang, D., Yang, Y., Zou, X., Zhang, J., Zheng, Z., & Wang, Z. (2020) · The Journals of Gerontology Series A · doi:10.1093/gerona/glaa214 · Cited by 87 · see citing works
Kamal, Z., Ullah, F., Ayaz, M., Sadiq, A., Ahmad, S., Zeb, A., Hussain, A., & Imran, M. (2015) · Biological Research · doi:10.1186/s40659-015-0011-1 · Cited by 86 · see citing works
20-Hydroxyecdysone Increases Fiber Size in a Muscle-Specific Fashion in Rat
Tóth, N., Szabó, A., Kacsala, P., Héger, J., & Zádor, E. (2008) · Phytomedicine · doi:10.1016/j.phymed.2008.04.015 · Cited by 85 · see citing works
Chikhi, I., Allali, H., Dib, M. E. A., Medjdoub, H., & Tabti, B. (2014) · Asian Pacific Journal of Tropical Disease · doi:10.1016/s2222-1808(14)60501-6 · Cited by 84 · see citing works
The complete 1H-NMR assignment of ecdysone and 20-hydroxyecdysone
Girault, J. P., & Lafont, R. (1988) · Journal of Insect Physiology · doi:10.1016/0022-1910(88)90080-7 · Cited by 78 · see citing works
Phytochemical Analysis of Pfaffia glomerata Inflorescences by LC-ESI-MS/MS
Felipe, D. F., Brambilla, L. Z. S., Porto, C., Pilau, E. J., & Cortez, D. (2014) · Molecules · doi:10.3390/molecules191015720 · Cited by 78 · see citing works
Chen, Q., Zhang, Y., Zhang, W., & Chen, Z. (2011) · Biomedical Chromatography · doi:10.1002/bmc.1614 · Cited by 78 · see citing works
Salih, E. Y. A., Fyhrquist, P., Abdalla, A. N., Abdelgadir, A. Y., Kanninen, M., Sipi, M., Luukkanen, O., Fahmi, M. K. M., Elamin, M. H., & Ali, H. (2017) · Antibiotics · doi:10.3390/antibiotics6040037 · Cited by 75 · see citing works
Expression and localization of estrogen receptor α in the C2C12 murine skeletal muscle cell line
Milanesi, L., de Boland, A. R., & Boland, R. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21706 · Cited by 64 · see citing works
Activity Guided Fractionation of Arum italicum Miller Tubers and the LC/MS-MS Profiles
(2017) · Records of Natural Products · doi:10.25135/rnp.06.17.05.089 · Cited by 63 · see citing works
Chernonosov, A. А., Karpova, E. A., & Lyakh, E. M. (2017) · Revista Brasileira de Farmacognosia · doi:10.1016/j.bjp.2017.07.001 · Cited by 60 · see citing works
Apigenin Enhances Skeletal Muscle Hypertrophy and Myoblast Differentiation by Regulating Prmt7
Jang, Y. J., Son, H. J., Choi, Y. M., Ahn, J., Jung, C. H., & Ha, T. Y. (2017) · Oncotarget · doi:10.18632/oncotarget.20962 · Cited by 59 · see citing works
Novotný, L., Abdel‐Hamid, M. E., Hamza, H., Masterova, I., & Grančai, D. (2003) · Journal of Pharmaceutical and Biomedical Analysis · doi:10.1016/s0731-7085(02)00706-9 · Cited by 56 · see citing works
Llorent-Martínez, E. J., Gouveia, S. C., & Castilho, P. C. (2014) · Industrial Crops and Products · doi:10.1016/j.indcrop.2014.10.068 · Cited by 55 · see citing works
Occurrence, biosynthesis, and putative role of ecdysteroids in plants
Adler, J. H., & Grebenok, R. J. (1999) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409239991209282 · Cited by 51 · cited 1× · see citing works
“The compound 20-hydroxyecdysone (20-HE) was identified with a structure identical to that isolated from insects [18].”
BackgroundRao, K. V. R., Mani, P., SATYANARAYANA, B., & Rao, T. R. (2017) · 3 Biotech · doi:10.1007/s13205-016-0581-9 · Cited by 51 · see citing works
Ecdysteroids in Plants and their Pharmacological Effects in Vertebrates and Humans
(2015) · Studies in Natural Products Chemistry · doi:10.1016/b978-0-444-63473-3.00005-8 · Cited by 48 · see citing works
Milanesi, L., Vasconsuelo, A., de Boland, A. R., & Boland, R. (2009) · Steroids · doi:10.1016/j.steroids.2009.01.005 · Cited by 47 · see citing works
Novel flavonoids with antioxidant activity from a Chenopodiaceous plant
Awaad, A. S., Maitland, D. J., Donia, A. E. R. M., Alqasoumi, S. I., & Soliman, G. A. (2011) · Pharmaceutical Biology · doi:10.3109/13880209.2011.591806 · Cited by 40 · see citing works
Phytochemical investigation on Atriplex halimus L. from Sardinia
Clauser, M., Dall’Acqua, S., Loi, M. C., & Innocenti, G. (2013) · Natural Product Research · doi:10.1080/14786419.2013.793684 · Cited by 38 · see citing works
Ben Nejma, A., Nguir, A., Ben Jannet, H., Hamza, M. A., Daïch, A., Othman, M., & Lawson, A. M. (2015) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2015.03.028 · Cited by 38 · see citing works
El‐Askary, H. I., Handoussa, H., Badria, F. A. A.-R., El‐Khatib, A. H., Alsayari, A., Linscheid, M. W., & Motaal, A. A. A. (2018) · Revista Brasileira de Farmacognosia · doi:10.1016/j.bjp.2018.10.001 · Cited by 36 · see citing works
Fábián, L., Argay, G., Kálmán, A., & Báthori, M. (2002) · Acta Crystallographica Section B Structural Science · doi:10.1107/s0108768102005608 · Cited by 35 · see citing works
Чермных, Н. С., Шимановский, Н. Л., Shutko, G. V., & Syrov, V. N. (1988) · PubMed · Cited by 34 · see citing works
Ommati, M. M., Farshad, O., Mousavi, K., Khalili, M., Jamshidzadeh, A., & Heidari, R. (2020) · Biologia · doi:10.2478/s11756-020-00429-7 · Cited by 34 · see citing works
El-Zahar, H., Menze, E. T., Handoussa, H., Osman, A. K., El‐Shazly, M., Mostafa, N. M., & Swilam, N. (2022) · Plants · doi:10.3390/plants11030455 · Cited by 31 · see citing works
Self-citationDetermination of triterpenoids from birch bark by liquid chromatography-tandem mass spectrometry
Kosyakov, D. S., Ul’yanovskii, N. V., & Falev, D. I. (2014) · Journal of Analytical Chemistry · doi:10.1134/s1061934814130061 · Cited by 29 · see citing works
Triterpenoids of Atriplex stocksii
Siddiqui, B. S., Ahmed, S., Ghiasuddin, & Khan, M. A.-U. (1994) · Phytochemistry · doi:10.1016/s0031-9422(00)89541-2 · Cited by 25 · see citing works
Boughalleb, N., Trabelsi, L., & Harzallah‐Skhiri, F. (2009) · Natural Product Research · doi:10.1080/14786410802168494 · Cited by 25 · see citing works
Cytotoxicity ofAtriplex confertifolia
Capua, C. J., Hopson, N. P., Stewart, C. M. M., Johnston, G. R., O'Neill, K. L., Schaalje, G. B., Lee, C. M., & Booth, G. M. (2010) · Journal of Toxicology · doi:10.1155/2010/976548 · Cited by 21 · see citing works
Ayoub, N., Badr, N., Al-Ghamdi, S. S., Alsanosi, S., Alzahrani, A. R., Abdel-Naim, A. B., Nematallah, K. A., & Swilam, N. (2021) · Nutrients · doi:10.3390/nu14010028 · Cited by 19 · see citing works
Self-citationPhytoecdysteroids from Atriplex nummularia
Keckeis, K., Sarker, S. D., & Dinan, L. N. (2000) · Fitoterapia · doi:10.1016/s0367-326x(99)00159-8 · Cited by 18 · see citing works
Atriplex mollis Desf. Aerial Parts: Extraction Procedures, Secondary Metabolites and Color Analysis
Boutaoui, N., Zaiter, L., Benayache, F., Benayache, S., Cacciagrano, F., Cesa, S., Secci, D., Carradori, S., Giusti, A. M., Campestre, C., et al. (2018) · Molecules · doi:10.3390/molecules23081962 · Cited by 18 · see citing works
El‐Aasr, M., Kabbash, A. M., El-Seoud, K. A. A., Ikeda, T., & Al-Madboly, L. A. (2016) · Cited by 18 · see citing works
Dimorphamides A – C, New Polyphenolic Amides from Atriplex dimorphostagia
Karim, A., Fatima, I., Hussain, S., & Malik, A. M. (2011) · Helvetica Chimica Acta · doi:10.1002/hlca.201000297 · Cited by 16 · see citing works
Phenolic composition and prospective anti-infectious properties of Atriplex lindleyi
Souda, S. S. E., Matloub, A. A., Nepveu, F., Valentin, A., & Roques, C. G. (2015) · Asian Pacific Journal of Tropical Disease · doi:10.1016/s2222-1808(15)60931-8 · Cited by 15 · see citing works
Structural Characterization of Polyphenolics in Livistona chinensis Using HPLC-PDA-MS
Ahmed, R. F., El-Khrisy, E. E.-D. A. M., El‐Kashak, W. A., Raey, M. A. E., Nassar, M. I., & Aboutabl, E.-S. (2019) · Journal of Advanced Pharmacy Research · doi:10.21608/aprh.2018.6527.1072 · Cited by 14 · see citing works
Effect of 20-hydroxyecdysone on proteolytic regulation in skeletal muscle atrophy
HIRUNSAI, M., YIMLAMAI, T., & SUKSAMRARN, A. (2016) · In Vivo · doi:10.21873/invivo.11007 · Cited by 13 · see citing works
Cristina, R. T., Hanganu, F., Dumitrescu, E., Муселин, Ф., Butnariu, M., Constantin, A., & Chiurciu, V. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109219 · Cited by 12 · see citing works
Isolation and characterization of flavonoid C-glycosides from Prosopis glandulosa Torr. leaves
Uv, B., Patel, N. A., Kumar, L. S., Gajera, J., Jadhav, A., & Muguli, G. (2018) · Pharmacognosy Magazine · doi:10.4103/pm.pm_505_17 · Cited by 11 · see citing works
Liu, R., Carballo-Arce, A. F., Singh, R., Saleem, A., Rocha, M. E. D. N., Mullally, M., Rojas, M. O., Alvarrez, L. P., Sanchez-Vindas, P. E., Garcia, M., et al. (2019) · Natural Product Communications · doi:10.1177/1934578x1901400104 · Cited by 11 · see citing works
Yusupova, U. Y., Usmanov, D. A., Azamatov, A. A., Ramazonov, N. S., & Jumadilla, R. (2020) · Natural Product Research · doi:10.1080/14786419.2020.1862834 · Cited by 11 · see citing works
SAMIR, M. D. A. F. M. S. M. (2019) · The Medical Journal of Cairo University/The Medical Journal of Cairo University · doi:10.21608/mjcu.2019.53950 · Cited by 10 · see citing works
Makisterone C-20,22-Acetonide from Rhaponticum uniflorum
Olennikov, D. N. (2018) · Chemistry of Natural Compounds · doi:10.1007/s10600-018-2515-8 · Cited by 7 · see citing works
Rybin, V., BOLTENKOV, E. V., & Новожилова, Е. В. (2007) · Natural Product Communications · doi:10.1177/1934578x0700201110 · Cited by 7 · see citing works
Quercetin Glycosides Improve Motor Performance and Muscle Weight in Adult Mice
Kanzaki, N., Takemoto, D., Ono, Y., Izumo, T., Shibata, H., Ye, X., Ingram, D. K., & Ye, J. (2019) · doi:10.35248/2155-9600.19.9.760 · Cited by 7 · see citing works
Lipids from Atriplex dimorphostegia leaves
Asilbekova, D. T., Tursunkhodzhaeva, F. M., & Gazizov, F. Y. (2008) · Chemistry of Natural Compounds · doi:10.1007/s10600-009-9181-9 · Cited by 4 · see citing works
Anabolic and androgenic effects of certain Atriplex species grown in Egypt
El‐Kersh, D. M., El-Sakhawy, F. S., Abou-Hussein, D. R., & Sleem, A. A. (2012) · Cited by 3 · see citing works
[Studies on the chemical constituents in seeds of Atriplex centralasiatica].
Zhang, Y., & Zhao, Y. (2005) · PubMed · Cited by 2 · see citing works
Chemical and Biological Investigation of Atriplex Canescens
Kumarihamy, M., Cutler, S., Tekwani, B., Chaurasya, N., & Muhammad, I. (2013) · Planta Medica · doi:10.1055/s-0033-1348716 · Cited by 1 · see citing works
Review: Theory and Practice of Histological Techniques, by John D. Bancroft and Alan Stevens
Mazur, J. E. (1978) · The American Biology Teacher · doi:10.2307/4446343 · Cited by 1 · see citing works
Dinan (1999) · doi:10.1002/(sici)1520-6327(1999)41:1
Flagged first, then by citations
1 of the 90 references couldn’t be matched to a known paper.
Research works printed but not linked: 6
- Zwetsloot, K.A., Committee Alan Utter, T.C., Member, M., Committee Kelly Cole, T.J., Poole, M.C., and Williams, C.D. (2017). Effects of Phytoecdysteroids on Skeletal Muscle Function and Protein Synthesis after Eccentric Damage. [Ph.D. Thesis, Appalachian State University].
- Gelin, 2003, CHENOPODIACEAE. Li Ke, Flora China, 5, 351
- Emam, 2011, Bioactive Constituents of Atriplex halimus Plant Shalabia, J. Nat. Prod., 4, 25
- Khalaf, 2011, LC/MS Analysis of Sterolic Compounds from Glycyrrhiza glabra, Stud. UBB Chem., 56, 97
- Hamed, 2014, el Chemo-protective effect on hepato-renal toxcicity and cytotoxic activity of lipoidal matter of atriplex lindleyi moq, Orig. Artic. Artic. Int. J. Pharm. Pharm. Sci., 6, 187
- Verma, 2011, Anabolic effect of Bombax ceiba linn. root in idiopathic involuntary weight loss—A case study, J. Herb. Med. Toxicol., 5, 1
Cited by
Sorted by citations
YAP represses the TEAD–NF-κB complex and inhibits the growth of clear cell renal cell carcinoma
Li, Z., Su, P., Yu, M., Zhang, X., Xu, Y., Jia, T., Yang, P., Zhang, C., Sun, Y., Li, X., et al. (2024) · Science Signaling · doi:10.1126/scisignal.adk0231 · Cited by 12 · see citing works
El‐Nashar, H. A. S., Al‐Qaaneh, A. M., Bhuia, M. S., Chowdhury, R., Abdel-Maksoud, M. A., Ebaid, H., Malik, A. R., Islam, M. T., Aufy, M., & Elhawary, E. A. (2024) · Frontiers in Chemistry · doi:10.3389/fchem.2024.1462309 · Cited by 9 · see citing works
Nie, X., Chen, M., Jin, C., Zhou, X., Yu, N., Lu, Y., & Meng, X. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.106228 · Cited by 8 · see citing works
Todorova, V., Ivanova, S., Yotov, V., Zaytseva, E., Ardasheva, R., Turiyski, V., Prissadova, N., & Ivanov, K. (2024) · Molecules · doi:10.3390/molecules29215145 · Cited by 7 · see citing works
Peptides of Yeast Saccharomyces cerevisiae Activated by the Aquatic Extract of Atriplex sibirica L.
Sergeeva, I., Permyakova, L., Markov, A., Рябоконева, Л. А., Atuchin∥⊥, V. V., Anshukov, A., Li, Y., & Proskuryakova, L. A. (2023) · ACS Food Science & Technology · doi:10.1021/acsfoodscitech.3c00455 · Cited by 7 · see citing works
Ak, G., Nilofar, N., Saka, E., Uba, A. İ., Rodrigues, M. J., Fernandes, E., Custódio, L. M. B., Yıldıztugay, E., Yapıcı, İ., Gülçın, İ., et al. (2025) · Zeitschrift für Naturforschung C · doi:10.1515/znc-2025-0220 · Cited by 3 · see citing works
Self-citationBatool, S., Hussain, I., Sheikh, M., Iqbal, M. A., Chin, K. L., Mahmood, S., Aftab, M., Khalid, M., Ahmad, F. J., Shaheen, N., et al. (2025) · New Journal of Chemistry · doi:10.1039/d5nj01089f · Cited by 1 · see citing works
Moussavou, G. N., Abogo, J. M., Nkolo, P., Moutsinga, M. M., Lemah-Yottoh, R.-K., Foundikou, H., Tsanyema-Bignoumba, B.-S., Obiang, C. S., Ella, B. E. N., Tchouya, G. R. F., et al. (2026) · Journal of the Indian Chemical Society · doi:10.1016/j.jics.2026.102974 · Cited by 1 · see citing works
Puri, S., Kashyap, U., Sharma, U. K., & Reddy, S. G. E. (2025) · Journal of Pest Science · doi:10.1007/s10340-025-01956-5
Chemical Constituents and Antimicrobial Activity of the Halophyte Atriplex leucoclada
Othman, A., Abdelkarem, F. M., Amen, Y. M., Abdulrahman, M. S., & Shimizu, K. (2026) · Natural Product Communications · doi:10.1177/1934578x261427064
Pharmacokinetic and Safety Profiles of Phytoecdysteroids in Mammals
Dinan, L. N., & Lafont, R. (2026) · Springer eBooks · doi:10.1007/978-981-95-8423-9_7
- Authors
- Zaghloul, E., Handousa, H., Singab, A. N. B., Elmazar, M. M., Ayoub, I. M., & Swilam, N.
- Affiliations
- British University in Egypt (EG)
- German University in Cairo (EG)
- Ain Shams University (EG)
- Department of Pharmacology, Faculty of Pharmacy, The British University in Egypt (BUE), Cairo 11837, Egypt
- Corresponding author
- Singab, Abdel Nasser B.
- Swilam, Noha
- Venue
- Plants
- Publisher
- MDPI AG
- Published
- 2023-01-03
- Volume
- 12
- Issue
- 1
- Pages
- 206
- ISSN
- 2223-7747 (ISSN-L)
- PMC
- PMC9824417
- OpenAlex
- W4313466471
- Cited by
- 11
- References
- 90
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 3 · 2023: 1
- FWCI
- 0.98
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Plants (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Phytochemical Studies and Bioactivities
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Medicinal Plants and Bioactive Compounds
- Keywords
- phytoecdysteroids, 20-hydroxyecdysone, anabolic activity, androgenic activity, orchiectomy, muscle mass, androgen receptor, polyphenols, triterpenoids, metabolite profiling
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review