Reconstituted mother tinctures of Gelsemium sempervirens L. improve memory and cognitive impairment in mice scopolamine-induced dementia model
Abstract
Ethnopharmacological relevance Gelsemium sempervirens (L.) J.St.-Hil is a herb used for the treatment of various neuroses in both homeopathic and Ayurvedic systems. The present study examines whether Gelsemium reconstituted tincture can protect against scopolamine induced cognitive discrepancies in amnesic mouse model. In order to investigate the protective mechanism of Gelsemium against dementia, in vitro acetyl cholinesterase and β-secretase enzyme inhibition and estimation of glutathione level in mouse brain were carried out.Materials and methods The inhibition study on acetyl cholinesterase and β-secretase enzyme was conducted on brain homogenate supernatant spectrophotometrically using specific substrate. Cognitive enhancement activity was assessed by elevated plus maze and passive avoidance study in scopolamine induced dementia mouse model. Glutathione, an anti-oxidant, was measured spectrophotometrically from scopolamine induced amnesic mice brain supernatant using 5,5'-dithiobis 2-nitrobenzoic acid in the presence and absence of Gelsemium tincture.Results Significant inhibition was found with Gelsemium on AChE and β-secretase enzyme with an IC50 of 9.25 and 16.25 µg/ml, respectively, followed by increasing glutathione levels in comparison to the untreated dementia group. The effect of Gelsemium of scopolamine-induced cognitive deficits was determined by measuring the behavioral parameters and the antioxidant status of the brain after scopolamine (1mg/kg i.p.) injected amnesic mice. Gelsemium significantly demonstrated in vivo anti-dementia activity (60% protection) and increased exploratory behavior.Conclusion Our investigations indicated that alkaloid, iridoids and coumarin enriched reconstituted Gelsemium tincture extract displays promising cognitive enhancement in adult mice after short-term oral treatment. Hence, Gelsemium can be a promising anti-dementia agent, mediating the protection against amnesia, attention disorders and learning dysfunctions through dual inhibition of both acetyl cholinesterases (no false positive effect was shown), β-secretase and antioxidant activity.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
Gelsemium sempervirens, Diospyros lotus, and Lavandula angustifolia improved cognitive performance and significantly reduced AChE activity.
“Other notable plant extracts, such as Gelsemium sempervirens, Diospyros lotus, and Lavandula angustifolia, have demonstrated improved cognitive performance and significant reductions in AChE activity, further supporting their potential neuroprotective benefits [59,60,61].”
From Cholinesterase Inhibitors from Plants and Their Potential in Alzheimer’s Treatment: Systematic Review (2025) · cites this paper as [59]
Cites
Bradford, M. M. (1976) · Analytical Biochemistry · doi:10.1016/0003-2697(76)90527-3 · Cited by 255,302 · see citing works
A new and rapid colorimetric determination of acetylcholinesterase activity
Ellman, G. L., Courtney, K. D., Andres, V., & Featherstone, R. M. (1961) · Biochemical Pharmacology · doi:10.1016/0006-2952(61)90145-9 · Cited by 27,221 · see citing works
The Amyloid Hypothesis of Alzheimer’s Disease: Progress and Problems on the Road to Therapeutics
Hardy, J., & Selkoe, D. J. (2002) · Science · doi:10.1126/science.1072994 · Cited by 13,864 · see citing works
Phytochemical Methods: A Guide to Modern Techniques of Plant Analysis
Harborne, J. B. (1973) · Cited by 5,306 · see citing works
The cholinergic hypothesis of Alzheimer’s disease: A review of progress
Francis, P. T., Palmer, A. M., Snape, M., & Wilcock, G. K. (1999) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.66.2.137 · Cited by 2,198 · cited 1× · see citing works
“Current status of therapeutic management of dementia related disorders is not satisfactory, as it has no permanent cure with existing medication (Francis et al., 1999; Figueiró et al., 2011).”
BackgroundModern Methods of Plant Analysis
Roark, R. C. (1956) · Journal of AOAC INTERNATIONAL · doi:10.1093/jaoac/39.3.895b · Cited by 2,194 · see citing works
Tau-mediated neurodegeneration in Alzheimer’s disease and related disorders
Ballatore, C., Lee, V. M.-Y., & Trojanowski, J. Q. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2194 · Cited by 2,174 · see citing works
Intracellular amyloid-β in Alzheimer's disease
LaFerla, F. M., Green, K. N., & Oddo, S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2168 · Cited by 1,942 · see citing works
Terry, A. V., & Buccafusco, J. J. (2003) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.102.041616 · Cited by 1,159 · see citing works
Raina, P., Santaguida, P., Ismaila, A., Patterson, C., Cowan, D., Levine, M., Booker, L., & Oremus, M. (2008) · Annals of Internal Medicine · doi:10.7326/0003-4819-148-5-200803040-00009 · Cited by 771 · see citing works
Treatment of Alzheimer's disease; current status and new perspectives
Scarpini, E. A., Scheltens, P., & Feldman, H. (2003) · The Lancet Neurology · doi:10.1016/s1474-4422(03)00502-7 · Cited by 720 · see citing works
Targeting acetylcholinesterase and butyrylcholinesterase in dementia
Lane, R. M., Potkin, S. G., & Enz, A. (2005) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145705005833 · Cited by 654 · see citing works
Cholinergic system during the progression of Alzheimer’s disease: therapeutic implications
Mufson, E. J., Counts, S., Perez, S. E., & Ginsberg, S. D. (2008) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.8.11.1703 · Cited by 589 · see citing works
The neuropsychology of down syndrome: evidence for hippocampal dysfunction.
Pennington, B. F., Moon, J., Edgin, J., Stedron, J., & Nadel, L. (2003) · Child Development · doi:10.1111/1467-8624.00522 · Cited by 514 · see citing works
Alzheimer’s disease pathogenesis and therapeutic interventions
Parihar, M. S., & Hemnani, T. (2004) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2003.12.007 · Cited by 434 · see citing works
A comparative study in rodents of standardized extracts of Bacopa monniera and Ginkgo biloba
Das, A., Shanker, G., Nath, C., Pal, R., Singh, S., & Singh, H. K. (2002) · Pharmacology Biochemistry and Behavior · doi:10.1016/s0091-3057(02)00940-1 · Cited by 264 · see citing works
Intracellular Aβ and cognitive deficits precede β-amyloid deposition in transgenic arcAβ mice
Knobloch, M., Konietzko, U., Krebs, D. C., & Nitsch, R. M. (2007) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2006.06.019 · Cited by 259 · see citing works
Elsherbiny, D. A., Khalifa, A. E., Attia, A. S., & Eldenshary, E. E.-D. S. (2003) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2003.09.014 · Cited by 219 · see citing works
Patil, P. O., Bari, S. B., Firke, S. D., Deshmukh, P. K., DONDA, S. T., & Patil, A. (2013) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2013.02.017 · Cited by 203 · see citing works
Memory enhancing effects of saffron in aged mice are correlated with antioxidant protection
Papandreou, M. A., Tsachaki, M., Efthimiopoulos, S., et al. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.01.007 · Cited by 195 · see citing works
Rhee, I. K., van Rijn, R. M., & Verpoorte, R. (2003) · Phytochemical Analysis · doi:10.1002/pca.675 · Cited by 186 · see citing works
Effect of rivastigmine on scopolamine-induced memory impairment in rats
Bejar, C., Wang, R.-H., & Weinstock, M. (1999) · European Journal of Pharmacology · doi:10.1016/s0014-2999(99)00643-3 · Cited by 176 · see citing works
Interactions between APP secretases and inflammatory mediators
Sastre, M., Walter, J., & Gentleman, S. (2008) · Journal of Neuroinflammation · doi:10.1186/1742-2094-5-25 · Cited by 172 · see citing works
Ożarowski, M., Mikołajczak, P. Ł., Bogacz, A., Gryszczyńska, A., Kujawska, M., Jodynis‐Liebert, J., Piasecka, A., Napieczyńska, H., Szulc, M., Kujawski, R., et al. (2013) · Fitoterapia · doi:10.1016/j.fitote.2013.09.012 · Cited by 170 · see citing works
Green tea catechins as a BACE1 (β-Secretase) inhibitor
Jeon, S.-Y., Bae, K., Seong, Y.-H., & Song, K. (2003) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2003.09.018 · Cited by 168 · see citing works
Kaizer, R. R., Corrêa, M. C., Spanevello, R. M., Morsch, V. M., Mazzanti, C. M., Gonçalves, J. F., & Schetinger, M. R. C. (2005) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2005.06.015 · Cited by 158 · see citing works
Jeong, E. J., Lee, K. Y., Kim, S. H., Sung, S. H., & Kim, Y. C. (2008) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2008.04.015 · Cited by 150 · see citing works
Bhattacharyya, S. S., Paul, S., Mandal, S. K., Banerjee, A., Boujedaini, N., & Khuda‐Bukhsh, A. R. (2009) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2009.04.015 · Cited by 119 · see citing works
Self-citationJung, H. A., Jin, S. E., Choi, R. J., Kim, D., Kim, Y. S., Ryu, J. H., Kim, D., Son, Y. K., Park, J. J., & Choi, J. S. (2010) · Life Sciences · doi:10.1016/j.lfs.2010.08.005 · Cited by 118 · see citing works
George, R. C., Lew, J., & Graves, D. J. (2013) · Journal of Alzheimer s Disease · doi:10.3233/jad-122113 · Cited by 112 · see citing works
Liu, R., Gao, M., Qiang, G., Zhang, T.-T., Lan, X., Ying, J., & Du, G.-H. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.009 · Cited by 106 · see citing works
Dose-effect study of Gelsemium sempervirens in high dilutions on anxiety-related responses in mice
Magnani, P., Conforti, A., Zanolin, E., Marzotto, M., & Bellavite, P. (2010) · Psychopharmacology · doi:10.1007/s00213-010-1855-2 · Cited by 104 · see citing works
Zhang, J., Gong, N., Huang, J., et al. (2013) · Pain · doi:10.1016/j.pain.2013.07.027 · Cited by 100 · see citing works
Tota, S., Kamat, P. K., Shukla, R., & Nath, C. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.02.041 · Cited by 88 · see citing works
Neurosteroids’ effects and mechanisms for social, cognitive, emotional, and physical functions
Frye, C. A. (2009) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2009.07.005 · Cited by 88 · see citing works
Function, regulation and therapeutic properties of β-secretase (BACE1)
Willem, M., Lammich, S., & Haass, C. (2009) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2009.01.003 · Cited by 86 · see citing works
Memantine Acts as a Cholinergic Stimulant in the Mouse Hippocampus
Drever, B. D., Anderson, W. G. L., Johnson, H., O’Callaghan, M. J., Seo, S., Choi, D.-Y., Riedel, G., & Platt, B. (2007) · Journal of Alzheimer s Disease · doi:10.3233/jad-2007-12405 · Cited by 69 · see citing works
Effect of high arsenic content in drinking water on rat brain.
Chaudhuri, A. N., Basu, S., Chattopadhyay, S., et al. (1999) · PubMed · Cited by 68 · see citing works
Nasal Colivelin Treatment Ameliorates Memory Impairment Related to Alzheimer's Disease
Yamada, M., Chiba, T., Sasabe, J., Terashita, K., Aiso, S., & Matsuoka, M. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301591 · Cited by 62 · see citing works
Antianxiety activity ofGelsemium sempervirens
Dutt, V., Dhar, V. J., & Sharma, A. (2010) · Pharmaceutical Biology · doi:10.3109/13880200903490521 · Cited by 57 · see citing works
Venard, C., Boujedaini, N., Belon, P., Mensah‐Nyagan, A. G., & Patte‐Mensah, C. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.02.009 · Cited by 53 · see citing works
9-hydroxy substituted iridoids from Gelsemium sempervirens
Jensen, S. R., Kirk, O., Nielsen, B. J., et al. (1987) · Phytochemistry · doi:10.1016/s0031-9422(00)82277-3 · Cited by 51 · see citing works
Role of molecular isoforms of acetylcholinesterase in learning and memory functions
DAS, A., Dikshit, M., & Nath, C. (2005) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2005.02.006 · Cited by 51 · see citing works
Darnaudéry, M., Pallarés, M., Piazza, P., Moal, M. L., & Mayo, W. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03166-9 · Cited by 49 · see citing works
Cytotoxic Steroids of Gelsemium sempervirens
Schun, Y., & Cordell, G. A. (1987) · Journal of Natural Products · doi:10.1021/np50050a012 · Cited by 47 · see citing works
Six new indole alkaloids from Gelsemium sempervirens Ait. f.
Kogure, N., Nishiya, C., Kitajima, M., et al. (2005) · Tetrahedron Letters · doi:10.1016/j.tetlet.2005.06.136 · Cited by 47 · see citing works
Neurobiological aspects of Alzheimer's disease
Chopra, K., Misra, S., & Kuhad, A. (2011) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2011.557363 · Cited by 46 · see citing works
Aremu, A. O., Amoo, S. O., Ndhlala, A. R., et al. (2011) · Food and Chemical Toxicology · doi:10.1016/j.fct.2011.02.003 · Cited by 45 · see citing works
Shinomol, G. K., Raghunath, N. R., Bharath, M. M. S., & ., M. (2013) · Central Nervous System Agents in Medicinal Chemistry · doi:10.2174/1871524911313010003 · Cited by 42 · see citing works
New Oxindole Alkaloids and Iridoid from Carolina jasmine (Gelsemium sempervirens AIT. f.)
Kitajima, M., Urano, A., Kogure, N., et al. (2003) · Chemical and Pharmaceutical Bulletin · doi:10.1248/cpb.51.1211 · Cited by 42 · see citing works
Peredery, O., & Persinger, M. A. (2004) · Phytotherapy Research · doi:10.1002/ptr.1511 · Cited by 38 · see citing works
Trinh, N.-H., Hoblyn, J., Mohanty, S., & Yaffe, K. (2003) · JAMA · doi:10.1001/jama.289.2.210 · Cited by 37 · see citing works
14β-Hydroxygelsedine, a New Oxindole Alkaloid from Gelsemium sempervirens
Schun, Y., & Cordell, G. A. (1985) · Journal of Natural Products · doi:10.1021/np50041a012 · Cited by 30 · see citing works
Hampel, H. J. (2012) · International Psychogeriatrics · doi:10.1017/s1041610212000579 · Cited by 30 · see citing works
Three oxindole alkaloids from Gelsemium species
Lin, L.-Z., Schun, Y., Cordell, G. A., et al. (1991) · Phytochemistry · doi:10.1016/0031-9422(91)83752-7 · Cited by 29 · see citing works
Figueiró, M., Ilha, J., Linck, V. M., Herrmann, A. P., Nardin, P., Menezes, C. B., Achaval, M., Gonçalves, C. A., Porciúncula, L. O., Nunes, D. S., et al. (2010) · Phytomedicine · doi:10.1016/j.phymed.2010.07.013 · Cited by 29 · see citing works
Steroids, Alkaloids, and Coumarins fromGelsemium sempervirens
Zhang, Z., Wang, P., Wei, Y., et al. (2008) · Planta Medica · doi:10.1055/s-0028-1088327 · Cited by 23 · see citing works
Anticholinesterase activities of cold and hot aqueous extracts ofF. racemosastem bark
Ahmed, F., & Urooj, A. (2010) · Pharmacognosy Magazine · doi:10.4103/0973-1296.62897 · Cited by 18 · see citing works
Bousta, D., Soulimani, R., Jarmouni, I. S., Belon, P., Aarab, L., Froment, N., & Younos, C. (2008) · Cited by 4 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
ALNasser, M. N., Alboraiy, G. M., Alsowig, E. M., & Alqattan, F. M. (2025) · Brain Sciences · doi:10.3390/brainsci15020215 · Cited by 35 · see citing works
- Authors
- Palit, P., Mukherjee, D., & Mandal, S. C.
- Affiliations
- Jadavpur University (IN)
- Venue
- Journal of Ethnopharmacology
- Publisher
- Elsevier BV
- Published
- 2015-01
- Volume
- 159
- Pages
- 274-284
- ISSN
- 0378-8741 (ISSN-L)
- OpenAlex
- W2093530701
- Cited by
- 25
- References
- 59
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2023: 6 · 2022: 2 · 2021: 2 · 2019: 3 · 2018: 3 · 2017: 4 · 2016: 2
- FWCI
- 4.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Ethnopharmacology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Complementary and alternative medicine › Medicinal Plants and Neuroprotection
- Health Sciences › Medicine › Pharmacology › Cholinesterase and Neurodegenerative Diseases
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- Gelsemium sempervirens, mother tincture, scopolamine-induced amnesia, cognitive impairment, dementia, acetylcholinesterase inhibition, beta-secretase inhibition, glutathione, antioxidant activity, memory enhancement, iridoids, coumarins, alkaloids, neuroprotection
- MeSH terms
- Acetylcholinesterase, Animals, Avoidance Learning, Behavior, Animal, Brain, Cognition Disorders, Dementia, Glutathione, Male, Phytotherapy, Memory, RNA, Messenger, Scopolamine, Aspartic Acid Endopeptidases, Toxicity Tests, Acute, Plant Preparations, Gelsemium, Mice, Amyloid Precursor Protein Secretases
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.
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