Natural Products and Bioprospecting ›› 2026, Vol. 16 ›› Issue (5): 75-75.DOI: 10.1007/s13659-026-00621-3
• REVIEWS • Previous Articles Next Articles
Shirsendu Nag Saikat1, Nawfal Hasan Siam2
Received:2025-11-20
Accepted:2026-02-11
Online:2026-10-08
Shirsendu Nag Saikat1, Nawfal Hasan Siam2
通讯作者:
Nawfal Hasan Siam,E-mail:nawfalhasansiam@gmail.com
Shirsendu Nag Saikat, Nawfal Hasan Siam. Translational potential of medicinal plants for Alzheimer’s disease: integrated evidence from molecular mechanisms to preclinical and clinical findings[J]. Natural Products and Bioprospecting, 2026, 16(5): 75-75.
Shirsendu Nag Saikat, Nawfal Hasan Siam. Translational potential of medicinal plants for Alzheimer’s disease: integrated evidence from molecular mechanisms to preclinical and clinical findings[J]. 应用天然产物, 2026, 16(5): 75-75.
| [1] Knopman DS, Amieva H, Petersen RC, Chételat G, Holtzman DM, Hyman BT, et al. Alzheimer disease. Nat Rev Dis Primers. 2021;7:33. https://doi.org/10.1038/s41572-021-00269-y. [2] Korczyn AD, Grinberg LT. Is Alzheimer disease a disease? Nat Rev Neurol. 2024;20:245-51. https://doi.org/10.1038/s41582-024-00940-4. [3] Abeysinghe AADT, Deshapriya RDUS, Udawatte C. Alzheimer’s disease; a review of the pathophysiological basis and therapeutic interventions. Life Sci. 2020;256:117996. https://doi.org/10.1016/j.lfs.2020.117996. [4] Matziorinis AM, Koelsch S. The promise of music therapy for Alzheimer’s disease: a review. Ann N Y Acad Sci. 2022;1516:11-7. https://doi.org/10.1111/nyas.14864. [5] Huang L-K, Chao S-P, Hu C-J. Clinical trials of new drugs for Alzheimer disease. J Biomed Sci. 2020;27:18. https://doi.org/10.1186/s12929-019-0609-7. [6] Huang L-K, Kuan Y-C, Lin H-W, Hu C-J. Clinical trials of new drugs for Alzheimer disease: a 2020-2023 update. J Biomed Sci. 2023;30:83. https://doi.org/10.1186/s12929-023-00976-6. [7] Calabrò M, Rinaldi C, Santoro G, Crisafulli C. The biological pathways of Alzheimer disease: a review. AIMS Neurosci. 2021;8:86-132. https://doi.org/10.3934/Neuroscience.2021005. [8] Better MA. Alzheimer’s disease facts and figures. Alzheimer’s Dement. 2018;2018(14):367-429. https://doi.org/10.1016/j.jalz.2018.02.001. [9] Yiannopoulou KG, Papageorgiou SG. Current and future treatments in Alzheimer Disease: an update. J Cent Nerv Syst Dis. 2020;12:117957352090739. https://doi.org/10.1177/1179573520907397. [10] Tiwari S, Atluri V, Kaushik A, Yndart A, Nair M. Alzheimer’s disease: pathogenesis, diagnostics, and therapeutics. Int J Nanomed. 2019;14:5541-54. https://doi.org/10.2147/IJN.S200490. [11] Tripathi P, Lodhi A, Rai S, Nandi N, Dumoga S, Yadav P, et al. Review of pharmacotherapeutic targets in Alzheimer’s disease and its management using traditional medicinal plants. Degener Neurol Neuromuscul Dis. 2024;14:47-74. https://doi.org/10.2147/DNND.S452009. [12] Gregory J, Vengalasetti YV, Bredesen DE, Rao RV. Neuroprotective herbs for the management of Alzheimer’s disease. Biomolecules. 2021;11:543. https://doi.org/10.3390/biom11040543. [13] Uddin MJ, Russo D, Rahman MM, Uddin SB, Halim MA, Zidorn C, et al. Anticholinesterase activity of eight medicinal plant species: in vitro and in silico studies in the search for therapeutic agents against Alzheimer’s disease. Evid Based Complement Altern Med. 2021;2021:1-14. https://doi.org/10.1155/2021/9995614. [14] Nagori K, Nakhate KT, Yadav K, Ajazuddin, Pradhan M. Unlocking the therapeutic potential of medicinal plants for Alzheimer’s disease: preclinical to clinical trial insights. Future Pharmacol. 2023;3:877-907. https://doi.org/10.3390/futurepharmacol3040053. [15] Dey A, Nandy S, Mukherjee A, Pandey DK. Plant natural products as neuroprotective nutraceuticals: preclinical and clinical studies and future implications. Proc Natl Acad Sci India Sect B Biol Sci. 2020;90:929-43. https://doi.org/10.1007/s40011-020-01170-6. [16] John OO, Amarachi IS, Chinazom AP, Adaeze E, Kale MB, Umare MD, et al. Phytotherapy: a promising approach for the treatment of Alzheimer’s disease. Pharmacol Res - Mod Chin Med. 2022;2:100030. https://doi.org/10.1016/j.prmcm.2021.100030. [17] Taqui R, Debnath M, Ahmed S, Ghosh A. Advances on plant extracts and phytocompounds with acetylcholinesterase inhibition activity for possible treatment of Alzheimer’s disease. Phytomed Plus. 2022;2:100184. https://doi.org/10.1016/j.phyplu.2021.100184. [18] Yu D-T, Li R-X, Sun J-R, Rong X-W, Guo X-G, Zhu G-D. Global mortality, prevalence and disability-adjusted life years of Alzheimer’s disease and other dementias in adults aged 60 years or older, and the impact of the COVID-19 pandemic: a comprehensive analysis for the global burden of disease 2021. BMC Psychiatry. 2025;25:503. https://doi.org/10.1186/s12888-025-06661-2. [19] Angelopoulou E, Paudel YN, Papageorgiou SG, Piperi C. APOE genotype and Alzheimer’s disease: the influence of lifestyle and environmental factors. ACS Chem Neurosci. 2021;12:2749-64. https://doi.org/10.1021/acschemneuro.1c00295. [20] Cui L, Hou N-N, Wu H-M, Zuo X, Lian Y-Z, Zhang C-N, et al. Prevalence of Alzheimer’s disease and Parkinson’s disease in China: an updated systematical analysis. Front Aging Neurosci. 2020. https://doi.org/10.3389/fnagi.2020.603854. [21] Rahman M, Tabassum A, Sultana S, Saha T, Nayeem MAJ, Jahan I, et al. Epidemiology and risk factors of Alzheimer’s disease and related dementias in South and Southeast Asia: a systematic review and meta-analysis protocol. BMJ Open. 2025;15:e105955. https://doi.org/10.1136/bmjopen-2025-105955. [22] Nadeem Zafar M. Epidemiology of Alzheimer’s disease and dementia in India: a systematic literature review. Med Sci Ukraine. 2025;21:133-41. https://doi.org/10.32345/2664-4738.2.2025.14. [23] Nianogo RA, Rosenwohl-Mack A, Yaffe K, Carrasco A, Hoffmann CM, Barnes DE. Risk factors associated with Alzheimer disease and related dementias by sex and race and ethnicity in the US. JAMA Neurol. 2022;79:584. https://doi.org/10.1001/jamaneurol.2022.0976. [24] Leahy TP, Simpson A, Sammon C, Ballard C, Gsteiger S. Estimating the prevalence of diagnosed Alzheimer disease in England across deprivation groups using electronic health records: a clinical practice research datalink study. BMJ Open. 2023;13:e075800. https://doi.org/10.1136/bmjopen-2023-075800. [25] Bonnechère B, Liu J, Thompson A, Amin N, van Duijn C. Does ethnicity influence dementia, stroke and mortality risk? Evidence from the UK Biobank. Front Public Health. 2023. https://doi.org/10.3389/fpubh.2023.1111321. [26] Dhana K, Beck T, Desai P, Wilson RS, Evans DA, Rajan KB. Prevalence of Alzheimer’s disease dementia in the 50 US states and 3142 counties: a population estimate using the 2020 bridged-race postcensal from the National Center for Health Statistics. Alzheimers Dement. 2023;19:4388-95. https://doi.org/10.1002/alz.13081. [27] Donkor DM, Marfo E, Bockarie A, Tettevi EJ, Antwi MH, Dogah J, et al. Genetic and environmental risk factors for dementia in African adults: a systematic review. Alzheimer’s Dement. 2025. https://doi.org/10.1002/alz.70220. [28] Chambers-Richards T, Chireh B, D’Arcy C. Trends in prevalence of self-reports of Alzheimer’s disease/dementia among non-institutionalized individuals 45+ in Canada, 1994-2014. J Public Health Res. 2022. https://doi.org/10.1177/22799036221135221. [29] Dobson AJ, Flicker L, Almeida OP, Waller M, Anstey K. Different estimates of the prevalence of dementia in Australia, 2021. Med J Aust. 2023;218:320-1. https://doi.org/10.5694/mja2.51838. [30] Cheung G, To E, Rivera-Rodriguez C, Ma’u E, Chan AHY, Ryan B, et al. Dementia prevalence estimation among the main ethnic groups in New Zealand: a population-based descriptive study of routinely collected health data. BMJ Open. 2022;12:e062304. https://doi.org/10.1136/bmjopen-2022-062304. [31] Amiri F, Safiri S, Shamekh A, Ebrahimi A, Sullman MJM, Kolahi A-A. Prevalence, deaths and disability-adjusted life years due to Alzheimer’s disease and other dementias in Middle East and North Africa, 1990-2021. Sci Rep. 2025;15:7058. https://doi.org/10.1038/s41598-025-89899-w. [32] Dhillon A, Fazal J. Overview and regional context of Alzheimer’s disease in the Middle East and North Africa region. Cureus. 2025. https://doi.org/10.7759/cureus.83164. [33] Ghajarbeygi P, Hajhoseini A, Hosseini M-S, Sharifan A. An in vitro and in vivo cholinesterase inhibitory activity of Pistacia khinjuk and Allium sativum essential oils. J Pharmacopuncture. 2019;22:231-8. https://doi.org/10.3831/kpi.2019.22.031. [34] Jung HY, Lee KY, Yoo DY, Kim JW, Yoo M, Lee S, et al. Essential oils from two Allium species exert effects on cell proliferation and neuroblast differentiation in the mouse dentate gyrus by modulating brain-derived neurotrophic factor and acetylcholinesterase. BMC Complement Altern Med. 2016. https://doi.org/10.1186/s12906-016-1384-6. [35] Choi J-H, Lee E-B, Jang H-H, Cha Y-S, Park Y-S, Lee S-H. Allium hookeri extracts improve Scopolamine-induced cognitive impairment via activation of the cholinergic system and anti-neuroinflammation in mice. Nutrients. 2021;13:2890. https://doi.org/10.3390/nu13082890. [36] Sushma, Sahu MR, Murugan NA, Mondal AC. Amelioration of amyloid-β induced Alzheimer’s disease by Bacopa monnieri through modulation of mitochondrial dysfunction and GSK-3β/Wnt/β-catenin signaling. Mol Nutr Food Res. 2024;68:e2300245. https://doi.org/10.1002/mnfr.202300245. [37] Saini N, Singh D, Sandhir R. Bacopa monnieri prevents colchicine-induced dementia by anti-inflammatory action. Metab Brain Dis. 2019;34:505-18. https://doi.org/10.1007/s11011-018-0332-1. [38] Palollathil A, Najar MA, Amrutha S, Pervaje R, Modi PK, Prasad TSK. Bacopa monnieri confers neuroprotection by influencing signaling pathways associated with interleukin 4, 13 and extracellular matrix organization in Alzheimer’s disease: a proteomics-based perspective. Neurochem Int. 2024;180:105864. https://doi.org/10.1016/j.neuint.2024.105864. [39] Ahmed HH, Mohamed EM, El-dsoki SM. Evidences for the promising therapeutic potential of Boswellia serrata against Alzheimer’s disease: pre-clinical study. Int J Pharm Pharm Sci. 2014;6:384-92. [40] Matthews DG, Khorani M, Bobe G, Caruso M, Magana AA, Gray NE, et al. Centella asiatica improves cognitive function and alters the hippocampal metabolome of aged Tg2576 and wild-type mice. J Alzheimers Dis Rep. 2024;8:1611-38. https://doi.org/10.1177/25424823241296740. [41] Chen C-L, Tsai W-H, Chen C-J, Pan T-M. Centella asiatica extract protects against amyloid β1-40-induced neurotoxicity in neuronal cells by activating the antioxidative defence system. J Tradit Complement Med. 2016;6:362-9. https://doi.org/10.1016/j.jtcme.2015.07.002. [42] Matthews DG, Caruso M, Murchison C, Zhu J, Wright KM, Harris C, et al. Centella asiatica improves memory and promotes antioxidative signaling in 5XFAD mice. Antioxidants Basel. 2019;8:630. https://doi.org/10.3390/antiox8120630. [43] Oh K-N, Bae D, Oh D-R, Hong J-A, Kim Y, Kim E, et al. TLR4/NF-κB-mediated anti-inflammatory and cognitive protective actions of Curcuma longa and Ar-turmerone in Alzheimer’s disease models. J Microbiol Biotechnol. 2025;35:e2506044. https://doi.org/10.4014/jmb.2506.06044. [44] Ahmed M, Ali SA, Hassan S, Raja R, Lodhi M, Mansoor N. Valuating the anti-Alzheimer potential of various plants’s extracts and their fractions through modulation of insulin fibrillation. J Popul Ther Clin Pharmacol. 2024;31:1653-69. https://doi.org/10.53555/m43wjc22. [45] Eun C-S, Lim J-S, Lee J, Lee S-P, Yang S-A. The protective effect of fermented Curcuma longa L. on memory dysfunction in oxidative stress-induced C6 gliomal cells, proinflammatory-activated BV2 microglial cells, and scopolamine-induced amnesia model in mice. BMC Complement Altern Med. 2017. https://doi.org/10.1186/s12906-017-1880-3. [46] Bharate SS, Kumar V, Singh G, Singh A, Gupta M, Singh D, et al. Preclinical development of Crocus sativus-based botanical lead IIIM-141 for Alzheimer’s disease: chemical standardization, efficacy, formulation development, pharmacokinetics, and safety pharmacology. ACS Omega. 2018;3:9572-85. https://doi.org/10.1021/acsomega.8b00841. [47] Patel KS, Dharamsi A, Priya M, Jain S, Mandal V, Girme A, et al. Saffron (Crocus sativus L.) extract attenuates chronic scopolamine-induced cognitive impairment, amyloid beta, and neurofibrillary tangles accumulation in rats. J Ethnopharmacol. 2024;326:117898. https://doi.org/10.1016/j.jep.2024.117898. [48] Batarseh YS, Bharate SS, Kumar V, Kumar A, Vishwakarma RA, Bharate SB, et al. Crocus sativus extract tightens the blood-brain barrier, reduces amyloid β load and related toxicity in 5XFAD mice. ACS Chem Neurosci. 2017;8:1756-66. https://doi.org/10.1021/acschemneuro.7b00101. [49] Liu X, Hao W, Qin Y, Decker Y, Wang X, Burkart M, et al. Long-term treatment with Ginkgo biloba extract EGb 761 improves symptoms and pathology in a transgenic mouse model of Alzheimer’s disease. Brain Behav Immun. 2015;46:121-31. https://doi.org/10.1016/j.bbi.2015.01.011. [50] Yu T, Xing Y, Gao Q, Wang D, Chen H, Wang H, et al. Ginkgo biloba extract drives gut flora and microbial metabolism variation in a mouse model of Alzheimer’s disease. Pharmaceutics. 2023;15:2746. https://doi.org/10.3390/pharmaceutics15122746. [51] Özşimşek A, Övey İS, Karaçay E, Yulug B. Protective and therapeutic role of Ginkgo biloba extract through TRPV1 channels in an in vitro Alzheimer’s disease model. Arch Neuropsychiatry. 2023. https://doi.org/10.29399/npa.28166. [52] Zavala-Ocampo LM, López-Camacho PY, Aguirre-Hernández E, Cárdenas-Vázquez R, Bonilla-Jaime H, Basurto-Islas G. Neuroprotective effects of Petiveria alliacea on scopolamine-induced learning and memory impairment mouse model. J Ethnopharmacol. 2024;318:116881. https://doi.org/10.1016/j.jep.2023.116881. [53] Valu M-V, Soare LC, Ducu C, Moga S, Negrea D, Vamanu E, et al. Hericium erinaceus (Bull.) Pers. ethanolic extract with antioxidant properties on scopolamine-induced memory deficits in a zebrafish model of cognitive impairment. J Fungi. 2021;7:477. https://doi.org/10.3390/jof7060477. [54] Trovato A, Siracusa R, Di Paola R, Scuto M, Ontario ML, Bua O, et al. Redox modulation of cellular stress response and lipoxin A4 expression by Hericium erinaceus in rat brain: relevance to Alzheimer’s disease pathogenesis. Immun Ageing. 2016. https://doi.org/10.1186/s12979-016-0078-8. [55] Ohba T, Yoshino Y, Ishisaka M, Abe N, Tsuruma K, Shimazawa M, et al. JapaneseHuperzia serrata extract and the constituent, huperzine A, ameliorate the scopolamine-induced cognitive impairment in mice. Biosci Biotechnol Biochem. 2015;79:1838-44. https://doi.org/10.1080/09168451.2015.1052773. [56] Dang TK, Hong S, Dao VT, Nguyen DT, Van NK, Nguyen HT, et al. Neuroprotective effects of total alkaloids fraction of Huperzia serrata on <scp>scopolamine-induced</scp> neurodegenerative animals. PTR Phytother Res/Phytother Res. 2022;37:140-50. https://doi.org/10.1002/ptr.7602. [57] Soodi M, Naghdi N, Hajimehdipoor H, Choopani S, Sahraei E. Memory-improving activity of Melissa officinalis extract in naïve and scopolamine-treated rats. Res Pharm Sci. 2015;9:107-14. [58] Zhang J, An S, Hu W, Teng M, Wang X, Qu Y, et al. The neuroprotective properties of Hericium erinaceus in glutamate-damaged differentiated PC12 cells and an Alzheimer’s disease mouse model. Int J Mol Sci. 2016;17:1810. https://doi.org/10.3390/ijms17111810. [59] Beheshti S, Shahmoradi B. Therapeutic effect of Melissa officinalis in an amyloid-β rat model of Alzheimer’s disease. J Herbmed Pharmacol. 2018;7:193-9. https://doi.org/10.15171/jhp.2018.31. [60] Andriana K, Nurdiana N, Barlianto W, Wiyasa IWA, Rahayu M. Effect of Nigella sativa L. extract on improving memory function through reducing GSK3β activation and Aβ42/40 ratio. J Pharm Pharmacogn Res. 2022;10:328-37. https://doi.org/10.56499/jppres21.1211_10.2.328. [61] Arslan SO, Uysal F, Koç A, Çam Özünlü SA. Nigella sativa oil attenuates neuroinflammation and cognitive deficits in a rat model of Alzheimer’s disease. Cukurova Med J. 2025;50:317-27. https://doi.org/10.17826/cumj.1588353. [62] Khan RU, Jawad SM, Kiyani MM, Shah SA, Bashir S, Khan H. Nigella sativa extract abrogates traumatic brain injury-induced memory impairment in adult mice. Heliyon. 2024;10:e38106. https://doi.org/10.1016/j.heliyon.2024.e38106. [63] Tran TL, Nguyen TH, Hang N, Phuong TT, Nguyen TT, Tran HL, et al. Neuroprotective effects of the ethanol extract of Salvia miltiorrhiza in Northern Vietnam against amyloid beta25-35-induced learning and memory impairment in vivo and cytotoxicity in vitro. Pharm Sci Asia. 2021;48:231-8. https://doi.org/10.29090/psa.2021.03.19.140. [64] Yuen CW, Murugaiyah V, Najimudin N, Azzam G. Danshen (Salvia miltiorrhiza) water extract shows potential neuroprotective effects in Caenorhabditis elegans. J Ethnopharmacol. 2021;266:113418. https://doi.org/10.1016/j.jep.2020.113418. [65] Kim M-S, Bang JH, Lee J, Kim HW, Sung SH, Han J-S, et al. Salvia miltiorrhiza extract protects white matter and the hippocampus from damage induced by chronic cerebral hypoperfusion in rats. BMC Complement Altern Med. 2015;15:415. https://doi.org/10.1186/s12906-015-0943-6. [66] Borai IH, Ezz MK, Rizk MZ, Aly HF, El-Sherbiny M, Matloub AA, et al. Therapeutic impact of grape leaves polyphenols on certain biochemical and neurological markers in AlCl3-induced Alzheimer’s disease. Biomed Pharmacother. 2017;93:837-51. https://doi.org/10.1016/j.biopha.2017.07.038. [67] Rapaka D, Bitra VR, Vishala TC, Akula A. Vitis vinifera acts as anti-Alzheimer’s agent by modulating biochemical parameters implicated in cognition and memory. J Ayurveda Integr Med. 2019;10:241-7. https://doi.org/10.1016/j.jaim.2017.06.013. [68] Duangjan C, Rangsinth P, Zhang S, Gu X, Wink M, Tencomnao T. Vitis vinifera leaf extract protects against glutamate-induced oxidative toxicity in HT22 hippocampal neuronal cells and increases stress resistance properties in Caenorhabditis elegans. Front Nutr. 2021. https://doi.org/10.3389/fnut.2021.634100. [69] Fuloria S, Mehta J, Chandel A, Sekar M, Rani NNIM, Begum MY, et al. A Comprehensive review on the therapeutic potential of Curcuma longa Linn. in relation to its major active constituent curcumin. Front Pharmacol. 2022;13:820806. https://doi.org/10.3389/fphar.2022.820806. [70] Moldoveanu C-A, Tomoaia-Cotisel M, Sevastre-Berghian A, Tomoaia G, Mocanu A, Pal-Racz C, et al. A review on current aspects of curcumin-based effects in relation to neurodegenerative, neuroinflammatory and cerebrovascular diseases. Molecules. 2024;30:43. https://doi.org/10.3390/molecules30010043. [71] Nunes YC, Mendes NM, Pereira E, Chehadi AC, Lamas CB, Haber S, et al. Curcumin: a golden approach to healthy aging: a systematic review of the evidence. Nutrients. 2024;16:2721. https://doi.org/10.3390/nu16162721. [72] Kou J, Wang M, Shi J-Z, Zhang H, Pu X, Song S, et al. Curcumin reduces cognitive deficits by inhibiting neuroinflammation through the endoplasmic reticulum stress pathway in Apolipoprotein E4 transgenic mice. ACS Omega. 2021;6:6654-62. https://doi.org/10.1021/acsomega.0c04810. [73] Shao S, Ye X, Su W, Wang Y. Curcumin alleviates Alzheimer’s disease by inhibiting inflammatory response, oxidative stress and activating the AMPK pathway. J Chem Neuroanat. 2023;134:102363. https://doi.org/10.1016/j.jchemneu.2023.102363. [74] Genchi G, Lauria G, Catalano A, Carocci A, Sinicropi MS. Neuroprotective effects of Curcumin in neurodegenerative diseases. Foods. 2024;13:1774. https://doi.org/10.3390/foods13111774. [75] Su W, Wang Y, Shao S, Ye X. Crocin ameliorates neuroinflammation and cognitive impairment in mice with Alzheimer’s disease by activating PI3K/AKT pathway. Brain Behav. 2024. https://doi.org/10.1002/brb3.3503. [76] Wani A, Al Rihani SB, Sharma A, Weadick B, Govindarajan R, Khan SU, et al. Crocetin promotes clearance of amyloid-β by inducing autophagy via the STK11/LKB1-mediated AMPK pathway. Autophagy. 2021;17:3813-32. https://doi.org/10.1080/15548627.2021.1872187. [77] Golpour- Hamedani S, Pourmasoumi M, Hejri Zarifi S, Askari G, Jamialahmadi T, Bagherniya M, et al. Therapeutic effects of saffron and its components on neurodegenerative diseases. Heliyon. 2024;10:e24334-e24334. https://doi.org/10.1016/j.heliyon.2024.e24334. [78] Li Y, Yuan X, Shen Y, Zhao J, Yue R, Liu F, et al. Bacopaside I ameliorates cognitive impairment in APP/PS1 mice via immune-mediated clearance of β-amyloid. Aging. 2016;8:521-33. https://doi.org/10.18632/aging.100913. [79] Ramasamy S, Chin SP, Sukumaran SD, Buckle MJC, Kiew LV, Chung LY. In silico and in vitro analysis of Bacoside A Aglycones and its derivatives as the constituents responsible for the cognitive effects of Bacopa monnieri. PLoS ONE. 2015;10:e0126565. https://doi.org/10.1371/journal.pone.0126565. [80] Callizot N, Campanari ML, Rouvière L, Jacquemot G, Henriques A, Garayev E, et al. Huperzia serrata extract ‘NSP01’ with neuroprotective effects-potential synergies of Huperzine A and polyphenols. Front Pharmacol. 2021;12:681532. https://doi.org/10.3389/fphar.2021.681532. [81] Zhu X, Xu J-B, Gao F, Wan L-X. Advances in the structural modification of Alzheimer’s disease drug—Huperzine A. Bioorg Chem. 2025;154:108012. https://doi.org/10.1016/j.bioorg.2024.108012. [82] Hashimoto M, Nakai T, Masutani T, Unno K, Akao Y. Improvement of learning and memory in Senescence-Accelerated Mice by S-Allylcysteine in mature garlic extract. Nutrients. 2020;12:1834. https://doi.org/10.3390/nu12061834. [83] Kaur S, Raj K, Gupta YK, Singh S. Allicin ameliorates aluminium- and copper-induced cognitive dysfunction in Wistar rats: relevance to neuro-inflammation, neurotransmitters and Aβ(1-42) analysis. JBIC J Biol Inorg Chem. 2021;26:495-510. https://doi.org/10.1007/s00775-021-01866-8. [84] Marefati N, Beheshti F, Vafaee F, Barabadi M, Hosseini M. The effects of incensole acetate on neuro-inflammation, brain-derived neurotrophic factor and memory impairment induced by lipopolysaccharide in rats. Neurochem Res. 2021;46:2473-84. https://doi.org/10.1007/s11064-021-03381-3. [85] Jebelli A, Khalaj-Kondori M, Bonyadi M, Ali M, Rahmati-Yamchi M. Beta-boswellic acid and ethanolic extract of olibanum regulating the expression levels of CREB-1 and CREB-2 Genes. PubMed. 2019;18:877-86. https://doi.org/10.22037/ijpr.2019.1100665. [86] Liu S, Chen L, Li J, Sun Y, Xu Y, Li Z, et al. Asiaticoside mitigates Alzheimer’s Disease pathology by attenuating inflammation and enhancing synaptic function. Int J Mol Sci. 2023;24:11976. https://doi.org/10.3390/ijms241511976. [87] Chalatsa I, Arvanitis DA, Koulakiotis NS, Giagini A, Skaltsounis AL, Papadopoulou-Daifoti Z, et al. The Crocus sativus compounds trans-Crocin 4 and trans-Crocetin modulate the amyloidogenic pathway and tau misprocessing in Alzheimer Disease neuronal cell culture models. Front Neurosci. 2019;13:249. https://doi.org/10.3389/fnins.2019.00249. [88] Sorrenti V, Contarini G, Sut S, Dall’Acqua S, Confortin F, Pagetta A, et al. Curcumin prevents acute neuroinflammation and long-term memory impairment induced by systemic lipopolysaccharide in mice. Front Pharmacol. 2018. https://doi.org/10.3389/fphar.2018.00183. [89] Xiang J, Yang F, Zhu W, Cai M, Li X-T, Zhang J-S, et al. Bilobalide inhibits inflammation and promotes the expression of Aβ degrading enzymes in astrocytes to rescue neuronal deficiency in AD models. Transl Psychiatry. 2021;11:1-8. https://doi.org/10.1038/s41398-021-01594-2. [90] Martínez-Mármol R, Chai Y, Conroy JN, Khan Z, Hong S, Kim SB, et al. Hericerin derivatives activates a pan-neurotrophic pathway in central hippocampal neurons converging to ERK1 /2 signaling enhancing spatial memory. J Neurochem. 2023. https://doi.org/10.1111/jnc.15767. [91] Yamamoto S, Kayama T, Noguchi-Shinohara M, Hamaguchi T, Yamada M, Abe K, et al. Rosmarinic acid suppresses tau phosphorylation and cognitive decline by downregulating the JNK signaling pathway. NPJ Sci Food. 2021;5:1. https://doi.org/10.1038/s41538-021-00084-5. [92] Kou J, Shi J, He Y, Hao J, Zhang H, Luo D, et al. Luteolin alleviates cognitive impairment in Alzheimer’s disease mouse model via inhibiting endoplasmic reticulum stress-dependent neuroinflammation. Acta Pharmacol Sin. 2021. https://doi.org/10.1038/s41401-021-00702-8. [93] Liang W, Zhao X, Feng J, Song F, Pan Y. Ursolic acid attenuates beta-amyloid-induced memory impairment in mice. Arq Neuropsiquiatr. 2016;74:482-8. https://doi.org/10.1590/0004-282x20160065. [94] Elibol B, Beker M, Terzioglu-Usak S, Dalli T, Kilic U. Thymoquinone administration ameliorates Alzheimer’s disease-like phenotype by promoting cell survival in the hippocampus of amyloid beta1-42 infused rat model. Phytomedicine. 2020;79:153324. https://doi.org/10.1016/j.phymed.2020.153324. [95] Tang Y, Huang D, Zhang M-H, Zhang W-S, Tang Y-X, Shi Z-X, et al. Salvianolic Acid B inhibits Aβ generation by modulating BACE1 activity in SH-SY5Y-APPsw cells. Nutrients. 2016;8:333. https://doi.org/10.3390/nu8060333. [96] Ding B, Lin C, Liu Q, He Y, Ruganzu JB, Jin H, et al. Tanshinone IIA attenuates neuroinflammation via inhibiting RAGE/NF-κB signaling pathway in vivo and in vitro. J Neuroinflamm. 2020. https://doi.org/10.1186/s12974-020-01981-4. [97] Choi J, Choi S-Y, Hong Y, Han Y-E, Oh S-J, Lee B, et al. The central administration of vitisin a, extracted from Vitis vinifera, improves cognitive function and related signaling pathways in a scopolamine-induced dementia model. Biomed Pharmacother. 2023;163:114812. https://doi.org/10.1016/j.biopha.2023.114812. [98] El-Saadony MT, Saad AM, Korma SA, Salem HM, El-Mageed TAA, Alkafaas SS, et al. Garlic bioactive substances and their therapeutic applications for improving human health: a comprehensive review. Front Immunol. 2024. https://doi.org/10.3389/fimmu.2024.1277074. [99] Tedeschi P, Nigro M, Travagli A, Catani M, Cavazzini A, Merighi S, et al. Therapeutic potential of allicin and aged garlic extract in Alzheimer’s disease. Int J Mol Sci. 2022;23:6950. https://doi.org/10.3390/ijms23136950. [100] Afolayan O, Nwaogu V, Idowu O, Dosumu O. Differential oxido-reductive activities of aged garlic extract and S-allyl-cysteine in genetically modified Drosophila model of Alzheimer’s disease. BMC Complement Med Ther. 2025. https://doi.org/10.1186/s12906-025-05093-5. [101] Bychowski M, Kwaśna J, Górski M, Załęska A, Kaźmierczyk I, Lenart K, et al. Recent advances in Bacopa monnieri research: neuroprotective effects and cognitive decline mitigation in neurodegenerative diseases with a focus on Alzheimer’s and Parkinson’s diseases. Qual Sport. 2024;35:56377. https://doi.org/10.12775/qs.2024.35.56377. [102] Valotto Neto LJ, Reverete de Araujo M, Moretti Junior RC, Mendes Machado N, Joshi RK, dos Santos Buglio D, et al. Investigating the neuroprotective and cognitive-enhancing effects of Bacopa monnieri: a systematic review focused on inflammation, oxidative stress, mitochondrial dysfunction, and apoptosis. Antioxidants. 2024;13:393. https://doi.org/10.3390/antiox13040393. [103] Dadhich A, Jain R, Sharma MM. Bacopa monnieri (L.) Wettst. plant extract mediated synthesis of metallic nanoparticles and regulation of bacoside-A-memory enhancer compound and their application: a comprehensive review. Plant Nano Biol. 2025;11:100133. https://doi.org/10.1016/j.plana.2024.100133. [104] Samuel K, Medikeri A, Pasha T, AnsariMoh F, Saudagar A. Centella asiatica: a traditional herbal medicine. World J Adv Res Rev. 2022;15:512-24. https://doi.org/10.30574/wjarr.2022.15.1.0726. [105] Aszrin FN, Adam SH, Mutalib MA, Tang HC, Gee S. An overview of Centella asiatica and its therapeutic applications. Life Sci Med Biomed. 2024. https://doi.org/10.28916/lsmb.8.1.2024.146. [106] Speers AB, García-Jaramillo M, Feryn A, Matthews DG, Lichtenberg T, Caruso M, et al. Centella asiatica alters metabolic pathways associated with Alzheimer’s disease in the 5xFAD mouse model of ß-amyloid accumulation. Front Pharmacol. 2021. https://doi.org/10.3389/fphar.2021.788312. [107] Wright KM, Bollen M, David J, Speers A, Brandes MS, Gray NE, et al. Pharmacokinetics and pharmacodynamics of key components of a standardized Centella asiatica product in cognitively impaired older adults: a phase 1, double-blind, randomized clinical trial. Antioxidants. 2022;11:215. https://doi.org/10.3390/antiox11020215. [108] Hein ZM, Gopalakrishna PK, Kanuri AK, Thomas W, Hussan F, Naik VR, et al. Centella asiatica: advances in extraction technologies. Phytochem Therap Appl. 2025;15:1081. https://doi.org/10.3390/life15071081. [109] Jiang J, Han R, Ren H, Yao Y, Jiang W. A review of neuroprotective properties of Centella asiatica (L.) Urb. and its therapeutic effects. Ann Med. 2025. https://doi.org/10.1080/07853890.2025.2559122. [110] Sultana A, Woo J. Structure-based identification of potent modulators from Centella asiatica targeting BACE-1. Heliyon. 2025;11:e42652-e42652. https://doi.org/10.1016/j.heliyon.2025.e42652. [111] Aissa R, Ibourki M, Ait Bouzid H, Bijla L, Oubannin S, Sakar EH, et al. Phytochemistry, quality control and medicinal uses of Saffron (Crocus sativus L.): an updated review. J Med Life. 2023;16:822-36. https://doi.org/10.25122/jml-2022-0353. [112] Anaeigoudari F, Anaeigoudari A, Kheirkhah-Vakilabad A. A review of therapeutic impacts of saffron (Crocus sativus L.) and its constituents. Physiol Rep. 2023. https://doi.org/10.14814/phy2.15785. [113] Yang W, Qiu X, Wu Q, Chang F, Zhou T, Zhou M, et al. Active constituents of saffron (Crocus sativus L.) and their prospects in treating neurodegenerative diseases (review). Exp Ther Med. 2023. https://doi.org/10.3892/etm.2023.11934. [114] Baluchnejadmojarad T, Mohamadi-Zarch S-M, Roghani M. Safranal, an active ingredient of saffron, attenuates cognitive deficits in amyloid β-induced rat model of Alzheimer’s disease: underlying mechanisms. Metab Brain Dis. 2019;34:1747-59. https://doi.org/10.1007/s11011-019-00481-6. [115] Kulić Ž, Lehner MD, Dietz GPH. Ginkgo biloba leaf extract EGb 761® as a paragon of the product by process concept. Front Pharmacol. 2022. https://doi.org/10.3389/fphar.2022.1007746. |
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