High-Altitude Medicinal Plants as Promising Source of Phytochemical Antioxidants to Combat Lifestyle-Associated Oxidative Stress-Induced Disorders
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Oxidative stress, driven by reactive oxygen, nitrogen, and sulphur species (ROS, RNS, RSS), poses a significant threat to cellular integrity and human health. Generated during mitochondrial respiration, inflammation, UV exposure and pollution, these species damage cells and contribute to pathologies like cardiovascular issues, neurodegeneration, cancer, and metabolic syndromes. Lifestyle factors exert a substantial influence on oxidative stress levels, with mitochondria emerging as pivotal players in ROS generation and cellular equilibrium. Phytochemicals, abundant in plants, such as carotenoids, ascorbic acid, tocopherols and polyphenols, offer diverse antioxidant mechanisms. They scavenge free radicals, chelate metal ions, and modulate cellular signalling pathways to mitigate oxidative damage. Furthermore, plants thriving in high-altitude regions are adapted to extreme conditions, and synthesize secondary metabolites, like flavonoids and phenolic compounds in bulk quantities, which act to form a robust antioxidant defence against oxidative stress, including UV radiation and temperature fluctuations. These plants are promising sources for drug development, offering innovative strategies by which to manage oxidative stress-related ailments and enhance human health. Understanding and harnessing the antioxidant potential of phytochemicals from high-altitude plants represent crucial steps in combating oxidative stress-induced disorders and promoting overall wellbeing. This study offers a comprehensive summary of the production and physio-pathological aspects of lifestyle-induced oxidative stress disorders and explores the potential of phytochemicals as promising antioxidants. Additionally, it presents an appraisal of high-altitude medicinal plants as significant sources of antioxidants, highlighting their potential for drug development and the creation of innovative antioxidant therapeutic approaches.
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The formation of copper deposits requires electron donation from a metallic reducing agent.
“These findings confirm that the formation of copper deposits requires electron donation from a metallic reducing agent [34], [35], [36], [37].”
From Identification of the Redox Reaction Between CuSO₄ and Zn Through Visual Observation in Basic Chemistry (2026) · cites this paper as [34]
The Introduction (§1.1.2) discusses electron transfer in mitochondrial ROS production, while §2 describes phytochemicals transferring electrons to neutralize radicals. Neither passage addresses copper deposits or a requirement for electron donation from a metallic reducing agent; searches for copper deposition and metallic reducing agents found no supporting passage in our copy. Page numbers were not available. (LLM, conf=0.74)
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- [1]Liguori I. Russo G. Curcio F. Bulli G. Aran L. Della-Morte D. Gargiulo G. Testa G. Cacciatore F. Bonaduce D. Oxidative Stress, Aging, and Diseases Clin. Interv. Aging 2018 13 757 772 10.2147/CIA.S158513 29731617 PMC5927356 · DOI · Paper page
- [3]Trachootham D. Lu W. Ogasawara M.A. Valle N.R.-D. Huang P. Redox Regulation of Cell Survival Antioxid. Redox Signal. 2008 10 1343 1374 10.1089/ars.2007.1957 18522489 PMC2932530 · DOI · Paper page
- [4]Birben E. Sahiner U.M. Sackesen C. Erzurum S. Kalayci O. Oxidative Stress and Antioxidant Defense World Allergy Organ. J. 2012 5 9 19 10.1097/WOX.0b013e3182439613 23268465 PMC3488923 · DOI
- [5]de Almeida A.J.P.O. de Oliveira J.C.P.L. da Silva Pontes L.V. de Souza Júnior J.F. Gonçalves T.A.F. Dantas S.H. de Almeida Feitosa M.S. Silva A.O. de Medeiros I.A. ROS: Basic Concepts, Sources, Cellular Signaling, and Its Implications in Aging Pathways Oxid. Med. Cell. Longev. 2022 2022 1225578 10.1155/2022/1225578 36312897 PMC9605829 · DOI
- [6]Fujii J. Homma T. Osaki T. Superoxide Radicals in the Execution of Cell Death Antioxidants 2022 11 501 10.3390/antiox11030501 35326151 PMC8944419 · DOI
- [7]Forcados G.E. Muhammad A. Oladipo O.O. Makama S. Meseko C.A. Metabolic Implications of Oxidative Stress and Inflammatory Process in SARS-CoV-2 Pathogenesis: Therapeutic Potential of Natural Antioxidants Front. Cell. Infect. Microbiol. 2021 11 654813 10.3389/fcimb.2021.654813 34123871 PMC8188981 · DOI
- [8]Masenga S.K. Kabwe L.S. Chakulya M. Kirabo A. Mechanisms of Oxidative Stress in Metabolic Syndrome Int. J. Mol. Sci. 2023 24 7898 10.3390/ijms24097898 37175603 PMC10178199 · DOI
- [9]Mudau F.N. Chimonyo V.G.P. Modi A.T. Mabhaudhi T. Neglected and Underutilised Crops: A Systematic Review of Their Potential as Food and Herbal Medicinal Crops in South Africa Front. Pharmacol. 2022 12 809866 10.3389/fphar.2021.809866 35126143 PMC8811033 · DOI
- [10]Juan C.A. Pérez de la Lastra J.M. Plou F.J. Pérez-Lebeña E. The Chemistry of Reactive Oxygen Species (ROS) Revisited: Outlining Their Role in Biological Macromolecules (DNA, Lipids and Proteins) and Induced Pathologies Int. J. Mol. Sci. 2021 22 4642 10.3390/ijms22094642 33924958 PMC8125527 · DOI · Paper page
- [11]Panday A. Sahoo M.K. Osorio D. Batra S. NADPH Oxidases: An Overview from Structure to Innate Immunity-Associated Pathologies Cell. Mol. Immunol. 2015 12 5 23 10.1038/cmi.2014.89 25263488 PMC4654378 · DOI · Paper page
- [12]Eguchi N. Vaziri N.D. Dafoe D.C. Ichii H. The Role of Oxidative Stress in Pancreatic β Cell Dysfunction in Diabetes Int. J. Mol. Sci. 2021 22 1509 10.3390/ijms22041509 33546200 PMC7913369 · DOI
- [13]Muscolo A. Mariateresa O. Giulio T. Mariateresa R. Oxidative Stress: The Role of Antioxidant Phytochemicals in the Prevention and Treatment of Diseases Int. J. Mol. Sci. 2024 25 3264 10.3390/ijms25063264 38542238 PMC10970659 · DOI
- [14]Zhu H. Liu C. Qian H. Pharmaceutical Potential of High-Altitude Plants for Fatigue-Related Disorders: A Review Plants 2022 11 2004 10.3390/plants11152004 35956482 PMC9370126 · DOI
- [15]Semwal P. Painuli S. Cruz-Martins N. Dioscorea Deltoidea Wall. Ex Griseb: A Review of Traditional Uses, Bioactive Compounds and Biological Activities Food Biosci. 2021 41 100969 10.1016/j.fbio.2021.100969 · DOI
- [16]Llauradó Maury G. Méndez Rodríguez D. Hendrix S. Escalona Arranz J.C. Fung Boix Y. Pacheco A.O. García Díaz J. Morris-Quevedo H.J. Ferrer Dubois A. Aleman E.I. Antioxidants in Plants: A Valorization Potential Emphasizing the Need for the Conservation of Plant Biodiversity in Cuba Antioxidants 2020 9 1048 10.3390/antiox9111048 33121046 PMC7693031 · DOI
- [17]Pizzino G. Irrera N. Cucinotta M. Pallio G. Mannino F. Arcoraci V. Squadrito F. Altavilla D. Bitto A. Oxidative Stress: Harms and Benefits for Human Health Oxid. Med. Cell. Longev. 2017 2017 8416763 10.1155/2017/8416763 28819546 PMC5551541 · DOI · Paper page
- [18]Bhattacharyya A. Chattopadhyay R. Mitra S. Crowe S.E. Oxidative Stress: An Essential Factor in the Pathogenesis of Gastrointestinal Mucosal Diseases Physiol. Rev. 2014 94 329 354 10.1152/physrev.00040.2012 24692350 PMC4044300 · DOI · Paper page
- [19]Phaniendra A. Jestadi D.B. Periyasamy L. Free Radicals: Properties, Sources, Targets, and Their Implication in Various Diseases Indian J. Clin. Biochem. 2015 30 11 26 10.1007/s12291-014-0446-0 25646037 PMC4310837 · DOI · Paper page
- [20]Checa J. Aran J.M. Reactive Oxygen Species: Drivers of Physiological and Pathological Processes J. Inflamm. Res. 2020 13 1057 1073 10.2147/JIR.S275595 33293849 PMC7719303 · DOI
- [22]Vona R. Pallotta L. Cappelletti M. Severi C. Matarrese P. The Impact of Oxidative Stress in Human Pathology: Focus on Gastrointestinal Disorders Antioxidants 2021 10 201 10.3390/antiox10020201 33573222 PMC7910878 · DOI · Paper page
- [24]Sharma P. Jha A.B. Dubey R.S. Pessarakli M. Reactive Oxygen Species, Oxidative Damage, and Antioxidative Defense Mechanism in Plants under Stressful Conditions J. Bot. 2012 2012 217037 10.1155/2012/217037 · DOI
- [25]Wang Y. Branicky R. Noë A. Hekimi S. Superoxide Dismutases: Dual Roles in Controlling ROS Damage and Regulating ROS Signaling J. Cell Biol. 2018 217 1915 1928 10.1083/jcb.201708007 29669742 PMC5987716 · DOI
- [26]Carraro E. Schilirò T. Biorci F. Romanazzi V. Degan R. Buonocore D. Verri M. Dossena M. Bonetta S. Gilli G. Physical Activity, Lifestyle Factors and Oxidative Stress in Middle Age Healthy Subjects Int. J. Environ. Res. Public Health 2018 15 1152 10.3390/ijerph15061152 29865194 PMC6025138 · DOI
- [28]Rani V. Deep G. Singh R.K. Palle K. Yadav U.C.S. Oxidative Stress and Metabolic Disorders: Pathogenesis and Therapeutic Strategies Life Sci. 2016 148 183 193 10.1016/j.lfs.2016.02.002 26851532 · DOI
- [29]Dubois-deruy E. Peugnet V. Turkieh A. Pinet F. Oxidative Stress in Cardiovascular Diseases Antioxidants 2020 9 864 10.3390/antiox9090864 32937950 PMC7554855 · DOI
- [30]Griendling K.K. Camargo L.L. Rios F.J. Alves-Lopes R. Montezano A.C. Touyz R.M. Oxidative Stress and Hypertension Circ. Res. 2021 128 993 1020 10.1161/CIRCRESAHA.121.318063 33793335 PMC8293920 · DOI
- [31]Murphy E. Liu J.C. Mitochondrial Calcium and Reactive Oxygen Species in Cardiovascular Disease Cardiovasc. Res. 2023 119 1105 1116 10.1093/cvr/cvac134 35986915 PMC10411964 · DOI
- [33]Wei Z. Li X. Li X. Liu Q. Cheng Y. Oxidative Stress in Parkinson’s Disease: A Systematic Review and Meta-Analysis Front. Mol. Neurosci. 2018 11 236 10.3389/fnmol.2018.00236 30026688 PMC6041404 · DOI
- [34]Davalli P. Marverti G. Lauriola A. D’Arca D. Targeting Oxidatively Induced DNA Damage Response in Cancer: Opportunities for Novel Cancer Therapies Oxid. Med. Cell. Longev. 2018 2018 2389523 10.1155/2018/2389523 29770165 PMC5892224 · DOI
- [35]Klaunig J.E. Oxidative Stress and Cancer Curr. Pharm. Des. 2019 24 4771 4778 10.2174/1381612825666190215121712 30767733 · DOI
- [36]Tangvarasittichai S. Oxidative Stress, Insulin Resistance, Dyslipidemia and Type 2 Diabetes Mellitus World J. Diabetes 2015 6 456 10.4239/wjd.v6.i3.456 25897356 PMC4398902 · DOI
- [37]Manna P. Jain S.K. Obesity, Oxidative Stress, Adipose Tissue Dysfunction, and the Associated Health Risks: Causes and Therapeutic Strategies Metab. Syndr. Relat. Disord. 2015 13 423 444 10.1089/met.2015.0095 26569333 PMC4808277 · DOI
- [38]Tan B.L. Norhaizan M.E. Liew W.-P.-P. Sulaiman Rahman H. Antioxidant and Oxidative Stress: A Mutual Interplay in Age-Related Diseases Front. Pharmacol. 2018 9 01162 10.3389/fphar.2018.01162 30405405 PMC6204759 · DOI
- [39]Dias T.R. Martin-Hidalgo D. Silva B.M. Oliveira P.F. Alves M.G. Endogenous and Exogenous Antioxidants As a Tool to Ameliorate Male Infertility Induced by Reactive Oxygen Species Antioxid. Redox Signal. 2020 33 767 785 10.1089/ars.2019.7977 32368933 · DOI
- [40]Moussa Z. Judeh Z.M.A. Ahmed S.A. Nonenzymatic Exogenous and Endogenous Antioxidants Free Radical Medicine and Biology IntechOpen London, UK 2020 10.5772/intechopen.87778 · DOI
- [41]Krishnamurthy P. Wadhwani A. Antioxidant Enzymes and Human Health Antioxidant Enzyme IntechOpen London, UK 2012 10.5772/48109 · DOI
- [42]Irato P. Santovito G. Enzymatic and Non-Enzymatic Molecules with Antioxidant Function Antioxidants 2021 10 579 10.3390/antiox10040579 33918542 PMC8070535 · DOI
- [43]Couto N. Wood J. Barber J. The Role of Glutathione Reductase and Related Enzymes on Cellular Redox Homoeostasis Network Free Radic. Biol. Med. 2016 95 27 42 10.1016/j.freeradbiomed.2016.02.028 26923386 · DOI
- [44]Cox G.M. Harrison T.S. McDade H.C. Taborda C.P. Heinrich G. Casadevall A. Perfect J.R. Superoxide Dismutase Influences the Virulence of Cryptococcus neoformans by Affecting Growth within Macrophages Infect. Immun. 2003 71 173 180 10.1128/IAI.71.1.173-180.2003 12496163 PMC143417 · DOI
- [45]Niki E. Oxidative Stress and Antioxidants: Distress or Eustress? Arch. Biochem. Biophys. 2016 595 19 24 10.1016/j.abb.2015.11.017 27095209 · DOI · Paper page
- [46]Bouayed J. Bohn T. Exogenous Antioxidants—Double-Edged Swords in Cellular Redox State: Health Beneficial Effects at Physiologic Doses versus Deleterious Effects at High Doses Oxid. Med. Cell. Longev. 2010 3 228 237 10.4161/oxim.3.4.12858 20972369 PMC2952083 · DOI · Paper page
- [47]Kasote D.M. Katyare S.S. Hegde M.V. Bae H. Significance of Antioxidant Potential of Plants and Its Relevance to Therapeutic Applications Int. J. Biol. Sci. 2015 11 982 991 10.7150/ijbs.12096 26157352 PMC4495415 · DOI
- [48]Sofowora A. Ogunbodede E. Onayade A. The Role and Place of Medicinal Plants in the Strategies for Disease Prevention Afr. J. Tradit. Complement. Altern. Med. 2013 10 210 229 10.4314/ajtcam.v10i5.2 24311829 PMC3847409 · DOI
- [49]Kumar A. Guleria S. Ghosh D. Dogra V. Kumar S. Managing Reactive Oxygen Species—Some Learnings from High Altitude Extremophytes Environ. Exp. Bot. 2021 189 104525 10.1016/j.envexpbot.2021.104525 · DOI
- [50]Das K. Roychoudhury A. Reactive Oxygen Species (ROS) and Response of Antioxidants as ROS-Scavengers during Environmental Stress in Plants Front. Environ. Sci. 2014 2 53 10.3389/fenvs.2014.00053 · DOI
- [51]Lee M.T. Lin W.C. Yu B. Lee T.T. Antioxidant Capacity of Phytochemicals and Their Potential Effects on Oxidative Status in Animals—A Review Asian-Australas. J. Anim. Sci. 2016 30 299 308 10.5713/ajas.16.0438 27660026 PMC5337908 · DOI
- [52]Ponnampalam E.N. Kiani A. Santhiravel S. Holman B.W.B. Lauridsen C. Dunshea F.R. The Importance of Dietary Antioxidants on Oxidative Stress, Meat and Milk Production, and Their Preservative Aspects in Farm Animals: Antioxidant Action, Animal Health, and Product Quality—Invited Review Animals 2022 12 3279 10.3390/ani12233279 36496798 PMC9738477 · DOI
- [53]Kumar A. P N. Kumar M. Jose A. Tomer V. Oz E. Proestos C. Zeng M. Elobeid T. K S. Major Phytochemicals: Recent Advances in Health Benefits and Extraction Method Molecules 2023 28 887 10.3390/molecules28020887 36677944 PMC9862941 · DOI · Paper page
- [54]González-Peña M.A. Ortega-Regules A.E. Anaya de Parrodi C. Lozada-Ramírez J.D. Chemistry, Occurrence, Properties, Applications, and Encapsulation of Carotenoids—A Review Plants 2023 12 313 10.3390/plants12020313 36679026 PMC9865331 · DOI
- [56]Yabuzaki J. Carotenoids Database: Structures, chemical fingerprints and distribution among organisms Database J. Biol. Databases Curation 2017 2017 bax004 10.1093/database/bax004 28365725 PMC5574413 · DOI
- [57]Merhan O. The Biochemistry and Antioxidant Properties of Carotenoids Carotenoids IntechOpen London, UK 2017 10.5772/67592 · DOI
- [58]Sindhu E.R. Kavya A.K. Binitha P.P. Role of Carotenoids in Preventing Oxidative Stress—Induced Cancer Handbook of Oxidative Stress in Cancer: Therapeutic Aspects Springer Singapore 2022 351 363 10.1007/978-981-16-5422-0_27 · DOI
- [59]Khoo H.-E. Prasad K.N. Kong K.-W. Jiang Y. Ismail A. Carotenoids and Their Isomers: Color Pigments in Fruits and Vegetables Molecules 2011 16 1710 1738 10.3390/molecules16021710 21336241 PMC6259627 · DOI
- [60]Tapiero H. Townsend D.M. Tew K.D. The Role of Carotenoids in the Prevention of Human Pathologies Biomed. Pharmacother. 2004 58 100 110 10.1016/j.biopha.2003.12.006 14992791 PMC6361147 · DOI
- [61]Ramel F. Birtic S. Cuiné S. Triantaphylidès C. Ravanat J.-L. Havaux M. Chemical Quenching of Singlet Oxygen by Carotenoids in Plants Plant Physiol. 2012 158 1267 1278 10.1104/pp.111.182394 22234998 PMC3291260 · DOI
- [62]Park H.-A. Hayden M.M. Bannerman S. Jansen J. Crowe-White K.M. Anti-Apoptotic Effects of Carotenoids in Neurodegeneration Molecules 2020 25 3453 10.3390/molecules25153453 32751250 PMC7436041 · DOI
- [63]Tan B.L. Norhaizan M.E. Carotenoids: How Effective Are They to Prevent Age-Related Diseases? Molecules 2019 24 1801 10.3390/molecules24091801 31075966 PMC6539799 · DOI
- [64]Maria A.G. Graziano R. Nicolantonio D. Carotenoids: Potential Allies of Cardiovascular Health? Food Nutr. Res. 2015 59 26762 10.3402/fnr.v59.26762 25660385 PMC4321000 · DOI
- [65]Mrowicka M. Mrowicki J. Kucharska E. Majsterek I. Lutein and Zeaxanthin and Their Roles in Age-Related Macular Degeneration—Neurodegenerative Disease Nutrients 2022 14 827 10.3390/nu14040827 35215476 PMC8874683 · DOI
- [66]Akram N.A. Shafiq F. Ashraf M. Ascorbic Acid-A Potential Oxidant Scavenger and Its Role in Plant Development and Abiotic Stress Tolerance Front. Plant Sci. 2017 8 613 10.3389/fpls.2017.00613 28491070 PMC5405147 · DOI
- [67]Flieger J. Flieger W. Baj J. Maciejewski R. Antioxidants: Classification, Natural Sources, Activity/Capacity Measurements, and Usefulness for the Synthesis of Nanoparticles Materials 2021 14 4135 10.3390/ma14154135 34361329 PMC8347950 · DOI
- [68]Gallie D.R. L-Ascorbic Acid: A Multifunctional Molecule Supporting Plant Growth and Development Scientifica 2013 2013 795964 10.1155/2013/795964 24278786 PMC3820358 · DOI
- [69]Hasanuzzaman M. Nahar K. Anee T.I. Fujita M. Glutathione in Plants: Biosynthesis and Physiological Role in Environmental Stress Tolerance Physiol. Mol. Biol. Plants 2017 23 249 268 10.1007/s12298-017-0422-2 28461715 PMC5391355 · DOI
- [70]Carr A. Maggini S. Vitamin C and Immune Function Nutrients 2017 9 1211 10.3390/nu9111211 29099763 PMC5707683 · DOI · Paper page
- [71]Gęgotek A. Skrzydlewska E. Antioxidative and Anti-Inflammatory Activity of Ascorbic Acid Antioxidants 2022 11 1993 10.3390/antiox11101993 36290716 PMC9598715 · DOI · Paper page
- [72]Morelli M.B. Gambardella J. Castellanos V. Trimarco V. Santulli G. Vitamin C and Cardiovascular Disease: An Update Antioxidants 2020 9 1227 10.3390/antiox9121227 33287462 PMC7761826 · DOI
- [73]Chambial S. Dwivedi S. Shukla K.K. John P.J. Sharma P. Vitamin C in Disease Prevention and Cure: An Overview Indian J. Clin. Biochem. 2013 28 314 328 10.1007/s12291-013-0375-3 24426232 PMC3783921 · DOI
- [74]Jiang Q. Natural Forms of Vitamin E: Metabolism, Antioxidant, and Anti-Inflammatory Activities and Their Role in Disease Prevention and Therapy Free Radic. Biol. Med. 2014 72 76 90 10.1016/j.freeradbiomed.2014.03.035 24704972 PMC4120831 · DOI
- [75]Almagro L. Sabater-Jara A.B. Belchí-Navarro S. Pedreño M.Á. Recent Trends in the Biotechnological Production of Tocopherols Using in Vitro Cultures Phytochem. Rev. 2021 20 1193 1207 10.1007/s11101-021-09742-8 · DOI
- [76]Pritam P. Deka R. Bhardwaj A. Srivastava R. Kumar D. Jha A.K. Jha N.K. Villa C. Jha S.K. Antioxidants in Alzheimer’s Disease: Current Therapeutic Significance and Future Prospects Biology 2022 11 212 10.3390/biology11020212 35205079 PMC8869589 · DOI
- [77]Szewczyk K. Chojnacka A. Górnicka M. Tocopherols and Tocotrienols—Bioactive Dietary Compounds; What Is Certain, What Is Doubt? Int. J. Mol. Sci. 2021 22 6222 10.3390/ijms22126222 34207571 PMC8227182 · DOI
- [78]Rizvi S. Raza S.T. Ahmed F. Ahmad A. Abbas S. Mahdi F. The Role of Vitamin e in Human Health and Some Diseases Sultan Qaboos Univ. Med. J. 2014 14 e157-65 24790736 PMC3997530
- [79]Rudrapal M. Khairnar S.J. Khan J. Dukhyil A.B. Ansari M.A. Alomary M.N. Alshabrmi F.M. Palai S. Deb P.K. Devi R. Dietary Polyphenols and Their Role in Oxidative Stress-Induced Human Diseases: Insights Into Protective Effects, Antioxidant Potentials and Mechanism(s) of Action Front. Pharmacol. 2022 13 806470 10.3389/fphar.2022.806470 35237163 PMC8882865 · DOI
- [80]Wu S. Chen W. Lu S. Zhang H. Yin L. Metabolic Engineering of Shikimic Acid Biosynthesis Pathway for the Production of Shikimic Acid and Its Branched Products in Microorganisms: Advances and Prospects Molecules 2022 27 4779 10.3390/molecules27154779 35897952 PMC9332510 · DOI
- [81]Kanner J. Food Polyphenols as Preventive Medicine Antioxidants 2023 12 2103 10.3390/antiox12122103 38136222 PMC10740609 · DOI
- [82]Lobo V. Patil A. Phatak A. Chandra N. Free Radicals, Antioxidants and Functional Foods: Impact on Human Health Pharmacogn. Rev. 2010 4 118 10.4103/0973-7847.70902 22228951 PMC3249911 · DOI · Paper page
- [83]Ullah A. Munir S. Badshah S.L. Khan N. Ghani L. Poulson B.G. Emwas A.-H. Jaremko M. Important Flavonoids and Their Role as a Therapeutic Agent Molecules 2020 25 5243 10.3390/molecules25225243 33187049 PMC7697716 · DOI · Paper page
- [84]Hassanein E.H.M. Althagafy H.S. Baraka M.A. Abd-alhameed E.K. Ibrahim I.M. Abd El-Maksoud M.S. Mohamed N.M. Ross S.A. The Promising Antioxidant Effects of Lignans: Nrf2 Activation Comes into View Naunyn Schmiedebergs Arch. Pharmacol. 2024 10.1007/s00210-024-03102-x PMC11422461 38695909 · DOI
- [85]Kumar N. Goel N. Phenolic Acids: Natural Versatile Molecules with Promising Therapeutic Applications Biotechnol. Rep. 2019 24 e00370 10.1016/j.btre.2019.e00370 31516850 PMC6734135 · DOI
- [86]Panche A.N. Diwan A.D. Chandra S.R. Flavonoids: An Overview J. Nutr. Sci. 2016 5 e47 10.1017/jns.2016.41 28620474 PMC5465813 · DOI
- [87]Dias M.C. Pinto D.C.G.A. Silva A.M.S. Plant Flavonoids: Chemical Characteristics and Biological Activity Molecules 2021 26 5377 10.3390/molecules26175377 34500810 PMC8434187 · DOI
- [88]Lü J. Lin P.H. Yao Q. Chen C. Chemical and Molecular Mechanisms of Antioxidants: Experimental Approaches and Model Systems J. Cell. Mol. Med. 2010 14 840 860 10.1111/j.1582-4934.2009.00897.x 19754673 PMC2927345 · DOI
- [89]Kumar S. Pandey A.K. Chemistry and Biological Activities of Flavonoids: An Overview Sci. World J. 2013 2013 162750 10.1155/2013/162750 24470791 PMC3891543 · DOI
- [90]Reinisalo M. Kårlund A. Koskela A. Kaarniranta K. Karjalainen R.O. Polyphenol Stilbenes: Molecular Mechanisms of Defence against Oxidative Stress and Aging-Related Diseases Oxid. Med. Cell. Longev. 2015 2015 340520 10.1155/2015/340520 26180583 PMC4477219 · DOI
- [91]Pinyaev S.I. Kuzmenko T.P. Revina N.V. Parchaykina M.V. Pronin A.S. Syusin I.V. Novozhilova O.S. Revin V.V. Chudaikina E.V. Revina E.S. Influence of Resveratrol on Oxidation Processes and Lipid Phase Characteristics in Damaged Somatic Nerves BioMed Res. Int. 2019 2019 2381907 10.1155/2019/2381907 31886183 PMC6927059 · DOI
- [92]Wang H.H. Liu M. Portincasa P. Wang D.Q.-H. Recent Advances in the Critical Role of the Sterol Efflux Transporters ABCG5/G8 in Health and Disease Lipid Transfer in Lipoprotein Metabolism and Cardiovascular Disease. Advances in Experimental Medicine and Biology Spinger Berlin/Heidelberg, Germany 2020 105 136 10.1007/978-981-15-6082-8_8 PMC8118135 32705597 · DOI
- [93]Bakrim S. Benkhaira N. Bourais I. Benali T. Lee L.-H. El Omari N. Sheikh R.A. Goh K.W. Ming L.C. Bouyahya A. Health Benefits and Pharmacological Properties of Stigmasterol Antioxidants 2022 11 1912 10.3390/antiox11101912 36290632 PMC9598710 · DOI · Paper page
- [94]Arivarasu L. In-Vitro Antioxidant Potential of Beta-Sitosterol: A Preface Cureus 2023 15 e45617 10.7759/cureus.45617 37868551 PMC10588763 · DOI
- [95]Li X. Xin Y. Mo Y. Marozik P. He T. Guo H. The Bioavailability and Biological Activities of Phytosterols as Modulators of Cholesterol Metabolism Molecules 2022 27 523 10.3390/molecules27020523 35056839 PMC8781140 · DOI
- [96]Hashim A.M. Alharbi B.M. Abdulmajeed A.M. Elkelish A. Hozzein W.N. Hassan H.M. Oxidative Stress Responses of Some Endemic Plants to High Altitudes by Intensifying Antioxidants and Secondary Metabolites Content Plants 2020 9 869 10.3390/plants9070869 32659963 PMC7412441 · DOI
- [97]Crupi P. Faienza M.F. Naeem M.Y. Corbo F. Clodoveo M.L. Muraglia M. Overview of the Potential Beneficial Effects of Carotenoids on Consumer Health and Well-Being Antioxidants 2023 12 1069 10.3390/antiox12051069 37237935 PMC10215867 · DOI
- [98]Mannino G. Di Stefano V. Lauria A. Pitonzo R. Gentile C. Vaccinium macrocarpon (Cranberry)-Based Dietary Supplements: Variation in Mass Uniformity, Proanthocyanidin Dosage and Anthocyanin Profile Demonstrates Quality Control Standard Needed Nutrients 2020 12 992 10.3390/nu12040992 32260055 PMC7230672 · DOI
- [99]Fagbohun O.F. Gillies C.R. Murphy K.P.J. Rupasinghe H.P.V. Role of Antioxidant Vitamins and Other Micronutrients on Regulations of Specific Genes and Signaling Pathways in the Prevention and Treatment of Cancer Int. J. Mol. Sci. 2023 24 6092 10.3390/ijms24076092 37047063 PMC10093825 · DOI
- [100]Cory H. Passarelli S. Szeto J. Tamez M. Mattei J. The Role of Polyphenols in Human Health and Food Systems: A Mini-Review Front. Nutr. 2018 5 370438 10.3389/fnut.2018.00087 PMC6160559 30298133 · DOI · Paper page
- [101]Chiang H.-M. Chen H.-C. Wu C.-S. Wu P.-Y. Wen K.-C. Rhodiola Plants: Chemistry and Biological Activity J. Food Drug Anal. 2015 23 359 369 10.1016/j.jfda.2015.04.007 28911692 PMC9351785 · DOI
- [102]Vezza T. Canet F. de Marañón A.M. Bañuls C. Rocha M. Víctor V.M. Phytosterols: Nutritional Health Players in the Management of Obesity and Its Related Disorders Antioxidants 2020 9 1266 10.3390/antiox9121266 33322742 PMC7763348 · DOI
- [103]Radomska-Leśniewska D.M. Skopiński P. Bałan B.J. Białoszewska A. Jóźwiak J. Rokicki D. Skopińska-Różewska E. Borecka A. Hevelke A. Review Paper Angiomodulatory Properties of Rhodiola spp. and other Natural Antioxidants Cent. Eur. J. Immunol. 2015 2 249 262 10.5114/ceji.2015.52839 PMC4637400 26557041 · DOI
- [104]Panth N. Paudel K.R. Parajuli K. Reactive Oxygen Species: A Key Hallmark of Cardiovascular Disease Adv. Med. 2016 2016 9152732 10.1155/2016/9152732 27774507 PMC5059509 · DOI
- [105]Münzel T. Camici G.G. Maack C. Bonetti N.R. Fuster V. Kovacic J.C. Impact of Oxidative Stress on the Heart and Vasculature J. Am. Coll. Cardiol. 2017 70 212 229 10.1016/j.jacc.2017.05.035 28683969 PMC5663297 · DOI
- [106]Padovan J.C. Dourado T.M.H. Pimenta G.F. Bruder-Nascimento T. Tirapelli C.R. Reactive Oxygen Species Are Central Mediators of Vascular Dysfunction and Hypertension Induced by Ethanol Consumption Antioxidants 2023 12 1813 10.3390/antiox12101813 37891892 PMC10604002 · DOI
- [107]Leventopoulos G. Koros R. Travlos C. Perperis A. Chronopoulos P. Tsoni E. Koufou E.-E. Papageorgiou A. Apostolos A. Kaouris P. Mechanisms of Atrial Fibrillation: How Our Knowledge Affects Clinical Practice Life 2023 13 1260 10.3390/life13061260 37374043 PMC10303005 · DOI
- [108]Chang X. Zhang T. Zhang W. Zhao Z. Sun J. Natural Drugs as a Treatment Strategy for Cardiovascular Disease through the Regulation of Oxidative Stress Oxid. Med. Cell. Longev. 2020 2020 5430407 10.1155/2020/5430407 33062142 PMC7537704 · DOI
- [110]Parham S. Kharazi A.Z. Bakhsheshi-Rad H.R. Nur H. Ismail A.F. Sharif S. RamaKrishna S. Berto F. Antioxidant, Antimicrobial and Antiviral Properties of Herbal Materials Antioxidants 2020 9 1309 10.3390/antiox9121309 33371338 PMC7767362 · DOI
- [111]Wilken R. Veena M.S. Wang M.B. Srivatsan E.S. Curcumin: A Review of Anti-Cancer Properties and Therapeutic Activity in Head and Neck Squamous Cell Carcinoma Mol. Cancer 2011 10 12 10.1186/1476-4598-10-12 21299897 PMC3055228 · DOI
- [112]Mokra D. Joskova M. Mokry J. Therapeutic Effects of Green Tea Polyphenol (—)-Epigallocatechin-3-Gallate (EGCG) in Relation to Molecular Pathways Controlling Inflammation, Oxidative Stress, and Apoptosis Int. J. Mol. Sci. 2022 24 340 10.3390/ijms24010340 36613784 PMC9820274 · DOI
- [113]Yang D. Wang T. Long M. Li P. Quercetin: Its Main Pharmacological Activity and Potential Application in Clinical Medicine Oxid. Med. Cell. Longev. 2020 2020 8825387 10.1155/2020/8825387 33488935 PMC7790550 · DOI
- [114]Zhang Y.J. Gan R.Y. Li S. Zhou Y. Li A.N. Xu D.P. Li H.B. Kitts D.D. Antioxidant Phytochemicals for the Prevention and Treatment of Chronic Diseases Molecules 2015 20 21138 21156 10.3390/molecules201219753 26633317 PMC6331972 · DOI · Paper page
- [115]Dobhal Y. Parcha V. Dhasmana D.C. Characterization of New Cardioprotective Principle Isolated from Methanolic Extract of Allium humile Leaves from Himalayan Region Bangladesh J. Pharmacol. 2016 11 383 10.3329/bjp.v11i2.25991 · DOI
- [116]Giuseppe D. Angela D. Davide R. Pamela M. Effects of a Combination of Berberis aristata, Silybum marianum and Monacolin on Lipid Profile in Subjects at Low Cardiovascular Risk; A Double-Blind, Randomized, Placebo-Controlled Trial Int. J. Mol. Sci. 2017 18 343 10.3390/ijms18020343 28178209 PMC5343878 · DOI
- [117]Habanova M. Saraiva J.A. Haban M. Schwarzova M. Chlebo P. Predna L. Gažo J. Wyka J. Intake of Bilberries (Vaccinium myrtillus L.) Reduced Risk Factors for Cardiovascular Disease by Inducing Favorable Changes in Lipoprotein Profiles Nutr. Res. 2016 36 1415 1422 10.1016/j.nutres.2016.11.010 27993193 · DOI
- [118]Karcheva-Bahchevanska D. Nikolova M. Iliev I. Inhibitory Potential of Different Bilberry (Vaccinium myrtillus L.) Extracts on Human Salivary α-Amylase Molecules 2023 28 5820 10.3390/molecules28155820 37570789 PMC10421460 · DOI
- [119]Sun X. Jia B. Sun J. Lin J. Lu B. Duan J. Li C. Wang Q. Zhang X. Tan M. Gastrodia elata Blume: A Review of Its Mechanisms and Functions on Cardiovascular Systems Fitoterapia 2023 167 105511 10.1016/j.fitote.2023.105511 37075984 · DOI
- [120]Chen F. Zhang H.-Y. He D. Rao C.-M. Xu B. Cardioprotective Effect of Gynostemma pentaphyllum against Streptozotocin Induced Cardiac Toxicity in Rats via Alteration of AMPK/Nrf2/HO-1 Pathway J. Oleo Sci. 2022 71 ess21281 10.5650/jos.ess21281 35781259 · DOI
- [121]Dai N. Zhao F. Fang M. Pu F. Kong L. Liu J. Gynostemma pentaphyllum for Dyslipidemia: A Systematic Review of Randomized Controlled Trials Front. Pharmacol. 2022 13 917521 10.3389/fphar.2022.917521 36091752 PMC9459123 · DOI
- [122]Wu M. Yu Z. Li X. Zhang X. Wang S. Yang S. Hu L. Liu L. Paeonol for the Treatment of Atherosclerotic Cardiovascular Disease: A Pharmacological and Mechanistic Overview Front. Cardiovasc. Med. 2021 8 690116 10.3389/fcvm.2021.690116 34368250 PMC8333700 · DOI
- [123]Zhang H. Chen L. Sun X. Yang Q. Wan L. Guo C. Matrine: A Promising Natural Product with Various Pharmacological Activities Front. Pharmacol. 2020 11 588 10.3389/fphar.2020.00588 32477114 PMC7232545 · DOI
- [124]Jung Y.A. Wan X. Yan H. Row K.H. Determination of Matrine and Oxymatrine in Sophora flavescens Ait. via High Performance Liquid Chromatography J. Liq. Chromatogr. Relat. Technol. 2008 31 2752 2761 10.1080/10826070802388326 · DOI
- [125]Janda K. Wojtkowska K. Jakubczyk K. Antoniewicz J. Skonieczna-Żydecka K. Passiflora incarnata in Neuropsychiatric Disorders—A Systematic Review Nutrients 2020 12 3894 10.3390/nu12123894 33352740 PMC7766837 · DOI
- [126]Achika J.I. Yusuf A.J. Ayo R.G. Liman D.U. Flavonoids from Nigerian Indigenous Medicinal Plants and Their Bioactivities: A Review Phytomed. Plus 2023 3 100405 10.1016/j.phyplu.2023.100405 · DOI
- [127]Lam K.Y. Ling A.P.K. Koh R.Y. Wong Y.P. Say Y.H. A Review on Medicinal Properties of Orientin Adv. Pharmacol. Sci. 2016 2016 4104595 10.1155/2016/4104595 27298620 PMC4889806 · DOI
- [128]Ding L. Liu Z. Zhao F. Bai G. Chen L. Yao X. Qiu F. Isolation and Identification of the Metabolites of Paeonol in Human Urine Xenobiotica 2012 42 1206 1212 10.3109/00498254.2012.694492 22680310 · DOI
- [129]Zhang M.-X. Huang X.-Y. Song Y. Xu W.-L. Li Y.-L. Li C. Astragalus propinquus Schischkin and Salvia miltiorrhiza Bunge Promote Angiogenesis to Treat Myocardial Ischemia via Ang-1/Tie-2/FAK Pathway Front. Pharmacol. 2023 13 1103557 10.3389/fphar.2022.1103557 36699092 PMC9868545 · DOI
- [130]Fan C. Sun X. Wang X. Yu H. Therapeutic Potential of the Chemical Composition of Dendrobium nobile Lindl Front. Pharmacol. 2023 14 1163830 10.3389/fphar.2023.1163830 37497110 PMC10366689 · DOI
- [131]Ren J. Fu L. Nile S.H. Zhang J. Kai G. Salvia miltiorrhiza in Treating Cardiovascular Diseases: A Review on Its Pharmacological and Clinical Applications Front. Pharmacol. 2019 10 753 10.3389/fphar.2019.00753 31338034 PMC6626924 · DOI
- [132]Jiang Z. Gao W. Huang L. Tanshinones, Critical Pharmacological Components in Salvia miltiorrhiza Front. Pharmacol. 2019 10 202 10.3389/fphar.2019.00202 30923500 PMC6426754 · DOI
- [133]Li D. Long Y. Yu S. Shi A. Wan J. Wen J. Li X. Liu S. Zhang Y. Li N. Research Advances in Cardio-Cerebrovascular Diseases of Ligusticum Chuanxiong Hort Front. Pharmacol. 2022 12 832673 10.3389/fphar.2021.832673 35173614 PMC8841966 · DOI
- [134]Lin J. Wang Q. Zhou S. Xu S. Yao K. Tetramethylpyrazine: A Review on Its Mechanisms and Functions Biomed. Pharmacother. 2022 150 113005 10.1016/j.biopha.2022.113005 35483189 · DOI
- [135]Jellinger K.A. Basic Mechanisms of Neurodegeneration: A Critical Update J. Cell. Mol. Med. 2010 10 457 487 10.1111/j.1582-4934.2010.01010.x PMC3823450 20070435 · DOI
- [136]Niedzielska E. Smaga I. Gawlik M. Moniczewski A. Stankowicz P. Pera J. Filip M. Oxidative Stress in Neurodegenerative Diseases Mol. Neurobiol. 2016 53 4094 4125 10.1007/s12035-015-9337-5 26198567 PMC4937091 · DOI · Paper page
- [138]Halliwell B. Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life Plant Physiol. 2006 141 312 322 10.1104/pp.106.077073 16760481 PMC1475431 · DOI
- [139]Singh A. Kukreti R. Saso L. Kukreti S. Oxidative Stress: A Key Modulator in Neurodegenerative Diseases Molecules 2019 24 1583 10.3390/molecules24081583 31013638 PMC6514564 · DOI
- [140]Alavi Naini S.M. Soussi-Yanicostas N. Tau Hyperphosphorylation and Oxidative Stress, a Critical Vicious Circle in Neurodegenerative Tauopathies? Oxid. Med. Cell. Longev. 2015 2015 151979 10.1155/2015/151979 26576216 PMC4630413 · DOI
- [141]Csala M. Kardon T. Legeza B. Lizák B. Mandl J. Margittai É. Puskás F. Száraz P. Szelényi P. Bánhegyi G. On the Role of 4-Hydroxynonenal in Health and Disease Biochim. Biophys. Acta (BBA) Mol. Basis Dis. 2015 1852 826 838 10.1016/j.bbadis.2015.01.015 25643868 · DOI
- [142]Brand-Yavin A. Yavin E. Brain Oxidative Stress from a Phospholipid Perspective Handbook of Neurochemistry and Molecular Neurobiology Springer Boston, MA, USA 2009 603 630 10.1007/978-0-387-30378-9_25 · DOI
- [144]Mishra S. Palanivelu K. The Effect of Curcumin (Turmeric) on Alzheimer′s Disease: An Overview Ann. Indian Acad. Neurol. 2008 11 13 10.4103/0972-2327.40220 19966973 PMC2781139 · DOI · Paper page
- [145]Rahman M.H. Akter R. Bhattacharya T. Abdel-Daim M.M. Alkahtani S. Arafah M.W. Al-Johani N.S. Alhoshani N.M. Alkeraishan N. Alhenaky A. Resveratrol and Neuroprotection: Impact and Its Therapeutic Potential in Alzheimer’s Disease Front. Pharmacol. 2020 11 619024 10.3389/fphar.2020.619024 33456444 PMC7804889 · DOI
- [146]Minocha T. Birla H. Obaid A.A. Rai V. Sushma P. Shivamallu C. Moustafa M. Al-Shehri M. Al-Emam A. Tikhonova M.A. Flavonoids as Promising Neuroprotectants and Their Therapeutic Potential against Alzheimer’s Disease Oxid. Med. Cell. Longev. 2022 2022 6038996 10.1155/2022/6038996 36071869 PMC9441372 · DOI
- [147]Kujawska M. Jodynis-Liebert J. Polyphenols in Parkinson’s Disease: A Systematic Review of In Vivo Studies Nutrients 2018 10 642 10.3390/nu10050642 29783725 PMC5986521 · DOI
- [148]Klomparens E. Ding Y. The Neuroprotective Mechanisms and Effects of Sulforaphane Brain Circ. 2019 5 74 10.4103/bc.bc_7_19 31334360 PMC6611193 · DOI
- [149]Wang J. Sun B.-L. Xiang Y. Tian D.-Y. Zhu C. Li W.-W. Liu Y.-H. Bu X.-L. Shen L.-L. Jin W.-S. Capsaicin Consumption Reduces Brain Amyloid-Beta Generation and Attenuates Alzheimer’s Disease-Type Pathology and Cognitive Deficits in APP/PS1 Mice Transl. Psychiatry 2020 10 230 10.1038/s41398-020-00918-y 32661266 PMC7359297 · DOI · Paper page
- [150]Magalingam K.B. Radhakrishnan A.K. Haleagrahara N. Protective Mechanisms of Flavonoids in Parkinson’s Disease Oxid. Med. Cell. Longev. 2015 2015 314560 10.1155/2015/314560 26576219 PMC4630416 · DOI
- [151]Chandran R. Abrahamse H. Identifying Plant-Based Natural Medicine against Oxidative Stress and Neurodegenerative Disorders Oxid. Med. Cell. Longev. 2020 2020 8648742 10.1155/2020/8648742 33014278 PMC7519196 · DOI
- [152]Uță G. Manolescu D.Ș. Avram S. Therapeutic Properties of Several Chemical Compounds of Salvia officinalis L. in Alzheimer’s Disease Mini-Rev. Med. Chem. 2021 21 1421 1430 10.2174/1389557521999201230200209 33390133 · DOI
- [153]Ariani A. Ghofar I. Khotimah H. Nurdiana N. Rahayu M. Asiatic Acid in Centella asiatica Extract towards Morphological Development in an Intermittent Hypoxia Intrauterine Embryo Model and Molecular Prediction Pathway of Insulin-like Growth Factor-1 (IGF-1) Receptor Signalling Open Vet. J. 2023 13 629 10.5455/OVJ.2023.v13.i5.16 37304601 PMC10257456 · DOI
- [154]Mushtaq Z. Imran M. Hussain M. Saeed F. Imran A. Umar M. Abdelgawad M.A. El-Ghorab A.H. Ahmed A. Alsagaby S.A. Asiatic Acid: A Review on Its Polypharmacological Properties and Therapeutic Potential against Various Maladies Int. J. Food Prop. 2023 26 1244 1263 10.1080/10942912.2023.2209702 · DOI
- [157]Fatima U. Roy S. Ahmad S. Al-Keridis L.A. Alshammari N. Adnan M. Islam A. Hassan M.I. Investigating Neuroprotective Roles of Bacopa Monnieri Extracts: Mechanistic Insights and Therapeutic Implications Biomed. Pharmacother. 2022 153 113469 10.1016/j.biopha.2022.113469 36076495 · DOI
- [158]Gubbannavar J. Chandola H. Harisha C. Khanpara K. Shukla V. A Comparative Pharmacognostical and Preliminary Physico-Chemical Analysis of Stem and Leaf of Bacopa monnieri (L.) Pennel and Bacopa Floribunda (R.BR.) Wettst AYU 2013 34 95 10.4103/0974-8520.115441 24049413 PMC3764889 · DOI
- [159]Gray N.E. Alcazar Magana A. Lak P. Wright K.M. Quinn J. Stevens J.F. Maier C.S. Soumyanath A. Centella asiatica: Phytochemistry and Mechanisms of Neuroprotection and Cognitive Enhancement Phytochem. Rev. 2018 17 161 194 10.1007/s11101-017-9528-y 31736679 PMC6857646 · DOI · Paper page
- [161]Ehrnhöfer-Ressler M.M. Fricke K. Pignitter M. Walker J.M. Walker J. Rychlik M. Somoza V. Identification of 1,8-Cineole, Borneol, Camphor, and Thujone as Anti-Inflammatory Compounds in a Salvia officinalis L. Infusion Using Human Gingival Fibroblasts J. Agric. Food Chem. 2013 61 3451 3459 10.1021/jf305472t 23488631 · DOI · Paper page
- [162]Ghorbani A. Esmaeilizadeh M. Pharmacological Properties of Salvia officinalis and Its Components J. Tradit. Complement. Med. 2017 7 433 440 10.1016/j.jtcme.2016.12.014 29034191 PMC5634728 · DOI · Paper page
- [163]Tundis R. Leporini M. Bonesi M. Rovito S. Passalacqua N.G. Salvia officinalis L. from Italy: A Comparative Chemical and Biological Study of Its Essential Oil in the Mediterranean Context Molecules 2020 25 5826 10.3390/molecules25245826 33321838 PMC7763040 · DOI
- [164]Shoukat S. Zia M.A. Uzair M. Attia K.A. Abushady A.M. Fiaz S. Ali S. Yang S.H. Ali G.M. Bacopa monnieri: A Promising Herbal Approach for Neurodegenerative Disease Treatment Supported by in Silico and in Vitro Research Heliyon 2023 9 e21161 10.1016/j.heliyon.2023.e21161 37954293 PMC10637926 · DOI
- [166]He Z. Hu Y. Niu Z. Zhong K. Liu T. Yang M. Ji L. Hu W. A Review of Pharmacokinetic and Pharmacological Properties of Asiaticoside, a Major Active Constituent of Centella asiatica (L.) Urb J. Ethnopharmacol. 2023 302 115865 10.1016/j.jep.2022.115865 36306932 · DOI · Paper page
- [167]Agnihotri V. Walia M. Pathania V. Singh B. Kant K. Evaluation of Antioxidant Activity of Picrorhiza kurroa (Leaves) Extracts Indian J. Pharm. Sci. 2013 75 324 10.4103/0250-474X.117438 24082348 PMC3783750 · DOI
- [168]Burchardt P. Żurawski J. Zuchowski B. Kubacki T. Murawa D. Wiktorowicz K. Wysocki H. State of the Art Paper Low-Density Lipoprotein, Its Susceptibility to Oxidation and the Role of Lipoprotein-Associated Phospholipase A2 and Carboxyl Ester Lipase Lipases in Atherosclerotic Plaque Formation Arch. Med. Sci. 2013 1 151 158 10.5114/aoms.2013.33176 23515030 PMC3598136 · DOI
- [169]Leopold J.A. Loscalzo J. Oxidative Mechanisms and Atherothrombotic Cardiovascular Disease Drug Discov. Today Ther. Strateg. 2008 5 5 13 10.1016/j.ddstr.2008.02.001 21048889 PMC2967043 · DOI
- [170]Savini I. Catani M. Evangelista D. Gasperi V. Avigliano L. Obesity-Associated Oxidative Stress: Strategies Finalized to Improve Redox State Int. J. Mol. Sci. 2013 14 10497 10538 10.3390/ijms140510497 23698776 PMC3676851 · DOI
- [171]Blagov A. Nedosugova L. Kirichenko T. Sukhorukov V. Melnichenko A. Orekhov A. Mitochondrial Dysfunction as a Factor of Energy Metabolism Disorders in Type 2 Diabetes Mellitus Front. Biosci. Sch. 2024 16 5 10.31083/j.fbs1601005 38538341 · DOI
- [172]Dludla P.V. Mabhida S.E. Ziqubu K. Nkambule B.B. Mazibuko-Mbeje S.E. Hanser S. Basson A.K. Pheiffer C. Kengne A.P. Pancreatic β-Cell Dysfunction in Type 2 Diabetes: Implications of Inflammation and Oxidative Stress World J. Diabetes 2023 14 130 146 10.4239/wjd.v14.i3.130 37035220 PMC10075035 · DOI
- [173]Holvoet P. Stress in Obesity and Associated Metabolic and Cardiovascular Disorders Scientifica 2012 2012 205027 10.6064/2012/205027 24278677 PMC3820434 · DOI
- [174]Moutia M. El Azhary K. Elouaddari A. Al Jahid A. Jamal Eddine J. Seghrouchni F. Habti N. Badou A. Capparis spinosa L. Promotes Anti-Inflammatory Response in Vitro through the Control of Cytokine Gene Expression in Human Peripheral Blood Mononuclear Cells BMC Immunol. 2016 17 26 10.1186/s12865-016-0164-x 27483999 PMC4969972 · DOI
- [175]Rocha D.H.A. Pinto D.C.G.A. Silva A.M.S. Macroalgae Specialized Metabolites: Evidence for Their Anti-Inflammatory Health Benefits Mar. Drugs 2022 20 789 10.3390/md20120789 36547936 PMC9783307 · DOI
- [176]Lourenço S.C. Moldão-Martins M. Alves V.D. Antioxidants of Natural Plant Origins: From Sources to Food Industry Applications Molecules 2019 24 4132 10.3390/molecules24224132 31731614 PMC6891691 · DOI
- [177]Cione E. La Torre C. Cannataro R. Caroleo M.C. Plastina P. Gallelli L. Quercetin, Epigallocatechin Gallate, Curcumin, and Resveratrol: From Dietary Sources to Human MicroRNA Modulation Molecules 2019 25 63 10.3390/molecules25010063 31878082 PMC6983040 · DOI
- [178]Ghafouri-Fard S. Shoorei H. Bahroudi Z. Hussen B.M. Talebi S.F. Taheri M. Ayatollahi S.A. Nrf2-Related Therapeutic Effects of Curcumin in Different Disorders Biomolecules 2022 12 82 10.3390/biom12010082 35053230 PMC8773597 · DOI
- [179]García-Martínez B.I. Ruiz-Ramos M. Pedraza-Chaverri J. Santiago-Osorio E. Mendoza-Núñez V.M. Effect of Resveratrol on Markers of Oxidative Stress and Sirtuin 1 in Elderly Adults with Type 2 Diabetes Int. J. Mol. Sci. 2023 24 7422 10.3390/ijms24087422 37108584 PMC10138491 · DOI
- [180]Xu D. Hu M.-J. Wang Y.-Q. Cui Y.-L. Antioxidant Activities of Quercetin and Its Complexes for Medicinal Application Molecules 2019 24 1123 10.3390/molecules24061123 30901869 PMC6470739 · DOI
- [182]Capece U. Moffa S. Improta I. Di Giuseppe G. Nista E.C. Cefalo C.M.A. Cinti F. Pontecorvi A. Gasbarrini A. Giaccari A. Alpha-Lipoic Acid and Glucose Metabolism: A Comprehensive Update on Biochemical and Therapeutic Features Nutrients 2022 15 18 10.3390/nu15010018 36615676 PMC9824456 · DOI
- [183]Yang S. Tao G. Yang L. Wu X. Liu J. Dagher F. Ou S. Song Y. Huang J. Dietary Phytochemical and Metabolic Disease Prevention: Focus on Plant Proteins Front. Nutr. 2023 10 1089487 10.3389/fnut.2023.1089487 36761228 PMC9905127 · DOI
- [184]Martchenko A. Papaelias A. Bolz S.-S. Physiologic Effects of the Maqui Berry (Aristotelia chilensis): A Focus on Metabolic Homeostasis Food Funct. 2024 15 4724 4740 10.1039/D3FO02524A 38618933 · DOI
- [185]Kunc N. Hudina M. Osterc G. Bavcon J. Ravnjak B. Mikulič-Petkovšek M. Phenolic Compounds of Rose Hips of Some Rosa Species and Their Hybrids Native Grown in the South-West of Slovenia during a Two-Year Period (2020–2021) Foods 2023 12 1952 10.3390/foods12101952 37238770 PMC10217035 · DOI
- [186]Oprica L. Bucsa C. Zamfirache M.M. Ascorbic Acid Content of Rose Hip Fruit Depending on Altitude Iran. J. Public Health 2015 44 138 139 26060787 PMC4450003
- [187]Gan R.-Y. Zhang D. Wang M. Corke H. Health Benefits of Bioactive Compounds from the Genus Ilex, a Source of Traditional Caffeinated Beverages Nutrients 2018 10 1682 10.3390/nu10111682 30400635 PMC6265843 · DOI
- [188]Louisa M. Patintingan C.G.H. Wardhani B.W.K. Moringa Oleifera Lam. in Cardiometabolic Disorders: A Systematic Review of Recent Studies and Possible Mechanism of Actions Front. Pharmacol. 2022 13 792794 10.3389/fphar.2022.792794 35431967 PMC9006177 · DOI
- [189]Wang F. Bao Y. Shen X. Zengin G. Lyu Y. Xiao J. Weng Z. Niazirin from Moringa oleifera Lam. Attenuates High Glucose-Induced Oxidative Stress through PKCζ/Nox4 Pathway Phytomedicine 2021 86 153066 10.1016/j.phymed.2019.153066 31447278 · DOI
- [190]Akaberi M. Hosseinzadeh H. Grapes (Vitis vinifera) as a Potential Candidate for the Therapy of the Metabolic Syndrome Phytother. Res. 2016 30 540 556 10.1002/ptr.5570 26800498 · DOI
- [191]Graf B.L. Raskin I. Cefalu W.T. Ribnicky D.M. Plant-Derived Therapeutics for the Treatment of Metabolic Syndrome Curr. Opin. Investig. Drugs 2010 11 1107 1115 20872313 PMC3755736
- [192]Wang Y. Zhang D. Ye W. Yin Z. Fung K.-P. Zhao S. Yao X. Triterpenoid Saponins from Androsace umbellata and Their Anti-Proliferative Activities in Human Hepatoma Cells Planta Med. 2008 74 1280 1284 10.1055/s-2008-1081291 18622900 · DOI
- [193]Xu D.-P. Li Y. Meng X. Zhou T. Zhou Y. Zheng J. Zhang J.-J. Li H.-B. Natural Antioxidants in Foods and Medicinal Plants: Extraction, Assessment and Resources Int. J. Mol. Sci. 2017 18 96 10.3390/ijms18010096 28067795 PMC5297730 · DOI
- [194]Dumanović J. Nepovimova E. Natić M. Kuča K. Jaćević V. The Significance of Reactive Oxygen Species and Antioxidant Defense System in Plants: A Concise Overview Front. Plant Sci. 2021 11 552969 10.3389/fpls.2020.552969 33488637 PMC7815643 · DOI
- [195]Askew E.W. Work at High Altitude and Oxidative Stress: Antioxidant Nutrients Toxicology 2002 180 107 119 10.1016/S0300-483X(02)00385-2 12324188 · DOI
- [196]Seleiman M.F. Al-Suhaibani N. Ali N. Akmal M. Alotaibi M. Refay Y. Dindaroglu T. Abdul-Wajid H.H. Battaglia M.L. Drought Stress Impacts on Plants and Different Approaches to Alleviate Its Adverse Effects Plants 2021 10 259 10.3390/plants10020259 33525688 PMC7911879 · DOI
- [197]Siyar S. Sami S. Majeed A. Heavy Metal Stress in Plants: Effects on Nutrients and Water Uptake Cellular and Molecular Phytotoxicity of Heavy Metals Springer Berlin/Heidelberg, Germany 2020 89 98 10.1007/978-3-030-45975-8_6 · DOI
- [198]Petrovska B. Historical Review of Medicinal Plants’ Usage Pharmacogn. Rev. 2012 6 1 10.4103/0973-7847.95849 22654398 PMC3358962 · DOI
- [199]Kaushik P. Ahlawat P. Singh K. Singh R. Chemical Constituents, Pharmacological Activities, and Uses of Common Ayurvedic Medicinal Plants: A Future Source of New Drugs Adv. Tradit. Med. 2021 23 673 714 10.1007/s13596-021-00621-3 · DOI
- [200]Butola J.S. Samant S.S. Saussurea Species in Indian Himalayan Region: Diversity, Distribution and Indigenous Uses Int. J. Plant Biol. 2010 1 e9 10.4081/pb.2010.e9 · DOI
- [201]Pandey M.M. Rastogi S. Rawat A.K.S. Saussurea costus: Botanical, Chemical and Pharmacological Review of an Ayurvedic Medicinal Plant J. Ethnopharmacol. 2007 110 379 390 10.1016/j.jep.2006.12.033 17306480 · DOI
- [202]Xing W. Wen C. Wang D. Shao H. Liu C. He C. Olatunji O.J. Cardiorenal Protective Effect of Costunolide against Doxorubicin-Induced Toxicity in Rats by Modulating Oxidative Stress, Inflammation and Apoptosis Molecules 2022 27 2122 10.3390/molecules27072122 35408518 PMC9000510 · DOI
- [203]Mlejnek P. Dolezel P. Kriegova E. Pastvova N. N-Acetylcysteine Can Induce Massive Oxidative Stress, Resulting in Cell Death with Apoptotic Features in Human Leukemia Cells Int. J. Mol. Sci. 2021 22 12635 10.3390/ijms222312635 34884437 PMC8657769 · DOI
- [204]Elshaer S.E. Hamad G.M. Hafez E.E. Baghdadi H.H. El-Demerdash F.M. Simal-Gandara J. Root Extracts of Saussurea costus as Prospective Detoxifying Food Additive against Sodium Nitrite Toxicity in Male Rats Food Chem. Toxicol. 2022 166 113225 10.1016/j.fct.2022.113225 35691462 · DOI
- [205]Jain R. Bhardwaj P. Pandey S.S. Kumar S. Arnebia euchroma, a Plant Species of Cold Desert in the Himalayas, Harbors Beneficial Cultivable Endophytes in Roots and Leaves Front. Microbiol. 2021 12 696667 10.3389/fmicb.2021.696667 34335527 PMC8322769 · DOI
- [206]Parray J.A. Kamili A.N. Jan S. Mir M.Y. Shameem N. Ganai B.A. Abd_Allah E.F. Hashem A. Alqarawi A.A. Manipulation of Plant Growth Regulators on Phytochemical Constituents and DNA Protection Potential of the Medicinal Plant Arnebia benthamii BioMed Res. Int. 2018 2018 6870139 10.1155/2018/6870139 29516007 PMC5817313 · DOI
- [207]Kumar A. Shashni S. Kumar P. Pant D. Singh A. Verma R.K. Phytochemical Constituents, Distributions and Traditional Usages of Arnebia euchroma: A Review J. Ethnopharmacol. 2021 271 113896 10.1016/j.jep.2021.113896 33524510 · DOI
- [208]Su L. Yan G. Guan B. Xu W. Hao Y. Wang Y. Zhang Y. Liu L. Shikonin Derivatives Protect Immune Organs from Damage and Promote Immune Responses In Vivo in Tumour-Bearing Mice Phytother. Res. 2012 26 26 33 10.1002/ptr.3503 21538626 · DOI
- [209]Ganie S.A. Dar T.A. Hamid R. Zargar O. Abeer S.U. Masood A. Amin S. Zargar M.A. In Vitro Antioxidant and Cytotoxic Activities of Arnebia benthamii (Wall Ex. G. Don): A Critically Endangered Medicinal Plant of Kashmir Valley Oxid. Med. Cell. Longev. 2014 2014 792574 10.1155/2014/792574 24734152 PMC3964854 · DOI
- [210]Shameem N. Kamili A.N. Parray J.A. Hamid R. Bandh S.A. Antimicrobial and Antioxidant Activity of Methanol Extracts of Arnebia benthamii (Wall Ex. G. Don) Johnston—A Critically Endangered Medicinal Plant of North Western Himalaya J. Anal. Sci. Technol. 2015 6 36 10.1186/s40543-015-0076-z · DOI
- [211]Papp N. Purger D. Czigle S. Czégényi D. Stranczinger S. Tóth M. Dénes T. Kocsis M. Takácsi-Nagy A. Filep R. The Importance of Pine Species in the Ethnomedicine of Transylvania (Romania) Plants 2022 11 2331 10.3390/plants11182331 36145732 PMC9506106 · DOI
- [212]Gülçin İ. Büyükokuroǧlu M.E. Oktay M. Küfrevioǧlu Ö.İ. Antioxidant and Analgesic Activities of Turpentine of Pinus nigra Arn. subsp. pallsiana (Lamb.) Holmboe J. Ethnopharmacol. 2003 86 51 58 10.1016/S0378-8741(03)00036-9 12686441 · DOI
- [213]Kurti F. Giorgi A. Beretta G. Mustafa B. Gelmini F. Testa C. Angioletti S. Giupponi L. Zilio E. Pentimalli D. Chemical Composition, Antioxidant and Antimicrobial Activities of Essential Oils of Different Pinus Species from Kosovo J. Essent. Oil Res. 2019 31 263 275 10.1080/10412905.2019.1584591 · DOI
- [214]Bisht A. Jain S. Misra A. Dwivedi J. Paliwal S. Sharma S. Cedrus deodara (Roxb. Ex D.Don) G.Don: A Review of Traditional Use, Phytochemical Composition and Pharmacology J. Ethnopharmacol. 2021 279 114361 10.1016/j.jep.2021.114361 34166738 · DOI
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- Authors
- Ashraf, M. V., Khan, S., Misri, S., Gaira, K. S., Rawat, S., Rawat, B., Khan, M. A. H., Shah, A. A., Asgher, M., & Ahmad, S.
- Affiliations
- Baba Ghulam Shah Badshah University (IN)
- G.B. Pant Institute of Himalayan Environment and Development (IN)
- Graphic Era University (IN)
- Corresponding author
- Asgher, Mohd
- Ahmad, Shoeb
- ORCID
- Venue
- Pharmaceuticals
- Publisher
- MDPI AG
- Published
- 2024-07-23
- Volume
- 17
- Issue
- 8
- Pages
- 975
- ISSN
- 1424-8247 (ISSN-L)
- PMC
- PMC11357401
- OpenAlex
- W4400983985
- Cited by
- 102
- References
- 419
- Citations by year
- 2026: 51 · 2025: 50 · 2024: 1
- FWCI
- 3.89
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Pharmaceuticals (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- University Grants Commission, New Delhi, India (F 30-459/2019(BSR))
- Topics
- Health Sciences › Medicine › Biochemistry › Phytochemicals and Antioxidant Activities
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Medicinal Plant Research
- Keywords
- oxidative stress, reactive oxygen species, reactive nitrogen species, reactive sulfur species, flavonoids, phenolic compounds, carotenoids, tocopherols, vitamin C, mitochondrial reactive oxygen species, ultraviolet radiation, lifestyle-related diseases, drug development, antioxidant defense
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