Gentiana lutea extract ameliorates scopolamine-induced amnesia in mice via cholinergic modulation and inhibition of Aβ/p-tau protein accumulation

Tripathi Rashmi , Sachdeva Monika , Kumar Nitin

Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (10) : 420 -431.

PDF
Asian Pacific Journal of Tropical Biomedicine ›› 2025, Vol. 15 ›› Issue (10) :420 -431. DOI: 10.4103/apjtb.apjtb_232_25
Original Article
research-article
Gentiana lutea extract ameliorates scopolamine-induced amnesia in mice via cholinergic modulation and inhibition of Aβ/p-tau protein accumulation
Author information +
History +
PDF

Abstract

Objective: To investigate the potential of hydro-alcoholic extract of Gentiana lutea roots (GLE) in scopolamine-induced amnesia model in mice.

Methods: The active chemical constituents were determined by GC-MS analysis. In vitro antioxidant activity was performed by the DPPH free radical scavenging method. Ex vivo anti-acetylcholinesterase assay was conducted to investigate the effect on the cholinergic system. A scopolamine-induced memory impairment model was used. The levels of beta-amyloid (Aβ) and tau protein were measured. The behavioral studies were performed through Morris water maze and passive avoidance learning tests, followed by estimation of biochemical markers (GSH and MDA), immunohistochemistry, and histopathological studies on isolated brain tissues.

Results: GLE exhibited DPPH free radical scavenging activity with an IC50 value of (76.68±2.28) μg/mL. GLE also manifested inhibitory effect on acetylcholinesterase [IC50 (36.58±0.73) μg/mL] to upregulate the cholinergic system. GLE at 200 mg/kg and 400 mg/kg significantly restored the memory impairment induced by scopolamine. GLE at 200 mg/kg and 400 mg/kg significantly reduced brain oxidative stress (P<0.001). Immunohistochemistry investigation showed a significant reduction in Aβ deposition and p-tau protein expression in the GLE treatment groups (P<0.001). Administration of GLE effectively reduced scopolamine-induced neuronal damage in a dose-dependent manner.

Conclusions: The study demonstrates that GLE ameliorates scopolamine-induced memory impairment by alleviating Aβ/p-tau protein accumulation and upregulation in the cholinergic system to improve cognitive dysfunction and behavioral problems.

Keywords

Amnesia / Beta amyloid / Scopolamine / Alzheimer’s disease / Acetylcholine / p-tau protein / Acetylcholinesterase / Gentiana lutea

Cite this article

Download citation ▾
Tripathi Rashmi, Sachdeva Monika, Kumar Nitin. Gentiana lutea extract ameliorates scopolamine-induced amnesia in mice via cholinergic modulation and inhibition of Aβ/p-tau protein accumulation. Asian Pacific Journal of Tropical Biomedicine, 2025, 15 (10) : 420-431 DOI:10.4103/apjtb.apjtb_232_25

登录浏览全文

4963

注册一个新账户 忘记密码

Conflict of interest statement

The authors declare that there is no conflict of interest.

Funding

The study received no extramural funding.

Data availability statement

The data supporting the findings of this study are available from the corresponding author upon request.

Authors’ contributions

TR conceptualized the study, conducted the experimental work, and data analysis, and drafted the manuscript. SM arranged all the necessary resources, supervised the investigation, and reviewed the manuscript. KN critically reviewed and edited the manuscript. All the authors reviewed and approved the final version of the manuscript.

Publisher’s note

The Publisher of the Journal remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Acknowledgments

The authors gratefully acknowledge the support of Raj Kumar Goel Institute of Technology (Pharmacy) management for providing the necessary research facilities that contributed significantly to the successful completion of this work.

References

[1]

Porsteinsson AP, Isaacson RS, Knox S, Sabbagh MN, Rubino I. Diagnosis of early Alzheimer’s disease: Clinical practice in 2021. J Prev Alzheimers Dis 2021; 8(3):371-386.

[2]

Choudhary A, Ranjan JK, Asthana HS. Prevalence of dementia in India: A systematic review and meta-analysis. Indian J Public Health 2021; 65(2):152-158.

[3]

Singh AK, Rai SN, Maurya A, Mishra G, Awasthi R, Shakya A, et al. Therapeutic potential of phytoconstituents in management of Alzheimer’s disease. Evid Based Complement Alternat Med 2021; 2021(1):1-19.

[4]

Mehla J, Gupta P, Pahuja M, Diwan D, Diksha D. Indian medicinal herbs and formulations for Alzheimer’s disease, from traditional knowledge to scientific assessment. Brain Sci 2020; 10(12):1-31.

[5]

Du X, Wang X, Geng M. Alzheimer’s disease hypothesis and related therapies. Transl Neurodegener 2018; 7:1-7.

[6]

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(4):877-907.

[7]

Pardo-Moreno T, González-Acedo A, Rivas-Domínguez A, García-Morales V, García-Cozar FJ, Ramos-Rodríguez JJ, et al. Therapeutic approach to Alzheimer’s disease: Current treatments and new perspectives. Pharmaceutics 2022; 14(6):1-20.

[8]

Du X, Wang X, Geng M. Alzheimer’s disease hypothesis and related therapies. Transl Neurodegener 2018; 7:1-7.

[9]

Bai R, Guo J, Ye XY, Xie Y, Xie T. Oxidative stress: The core pathogenesis and mechanism of Alzheimer’s disease. Ageing Res Rev 2022; 77. doi: 1016/j.arr.2022.101619.

[10]

San Tang K. The cellular and molecular processes associated with scopolamine-induced memory deficit: A model of Alzheimer’s biomarkers. Life Sci 2019; 233:1-6.

[11]

Kinney JW, Bemiller SM, Murtishaw AS, Leisgang AM, Salazar AM, Lamb BT. Inflammation as a central mechanism in Alzheimer’s disease. Alzheimers Dement 2018; 4:575-590.

[12]

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(4):877-907.

[13]

Prakash O, Singh R, Kumar S, Srivastava S, Ved A. Gentiana lutea Linn. (yellow gentian): A comprehensive. J Ayurvedic Herb Med 2017; 3:175-181.

[14]

Pan Y, Zhao YL, Zhang J, Li WY, Wang YZ. Phytochemistry and pharmacological activities of the genus Gentiana (Gentianaceae). Chem Biodiversity 2016; 13:107-150.

[15]

Cafaro T, Carnicelli V, Caprioli G, Maggi F, Celenza G, Perilli M, et al. Anti-apoptotic and anti-inflammatory activity of Gentiana lutea root extract. Adv Trad Med 2020; 20:619-630.

[16]

Mustafa AM, Caprioli G, Dikmen M, Kaya E, Maggi F, Sagratini G, et al. Evaluation of neuritogenic activity of cultivated, wild and commercial roots of Gentiana lutea L. J Funct Foods 2015; 19:164-173.

[17]

Yang M, Zhou KY, Li FF, Yang HY, Yin M, Zhang LH, et al. Effects of Gentiana delavayi flower extract on APP processing in APP/PS1 CHO cells. Biol Pharm Bull 2020; 43(5):767-773.

[18]

Nastasijević B, Lazarević-Pašti T, Dimitrijević-Branković S, Pašti I, Vujačić A, Joksić G, et al. Inhibition of myeloperoxidase and antioxidative activity of Gentiana lutea extracts. J Pharm Biomed Anal Open 2012; 66:191-196.

[19]

Sharma T, Pandey B, Shrestha BK, Koju GM, Thusa R, Karki N. Phytochemical screening of medicinal plants and study of the effect of phytoconstituents in seed germination. Tribh Univ J 2020; 35(2):1-11.

[20]

Genwali GR, Acharya PP, Rajbhandari M. Isolation of gallic acid and estimation of total phenolic content in some medicinal plants and their antioxidant activity. Nepal J Sci Technol 2013; 14(1):95-102.

[21]

Tepal P. Phytochemical screening, total flavonoid and phenolic content assays of various solvent extracts of tepal of Musa paradisiaca. MJAS 2016; 20(5):1181-1190.

[22]

Sundaram DP, Govindaswamy S, KS SS, Selvamani P, Latha S. Aristolochia bracteolata Lam’s toxicity profile and neuroprotective effects in mice with memory impairment triggered by scopolamine. J Pharmacol Pharmacother 2023; 14(3):238-245.

[23]

Asaduzzaman M, Uddin MJ, Kader MA, Alam AH, Rahman AA, Rashid M, et al. In vitro acetylcholinesterase inhibitory activity and the antioxidant properties of Aegle marmelos leaf extract: Implications for the treatment of Alzheimer’s disease. Psychogeriatrics 2014; 14(1):1-10.

[24]

Islam MA, Zaman S, Biswas K, Al-Amin MY, Hasan MK, Alam AH, et al. Evaluation of cholinesterase inhibitory and antioxidant activity of Wedelia chinensis and isolation of apigenin as an active compound. BMC Complement Med Ther 2021; 21:1-12.

[25]

OECD Guidelines for the testing of chemicals, revised draft guidelines 423: Acute Oral toxicity- Acute toxic class method.Revised document. CPCSEA, Ministry of Social Justice and Empowerment, Govt. of India; 2000.

[26]

Gupta R, Singh HK. Nootropic potential of Alternanthera sessilis and Clerodendrum infortunatum leaves on mice. Asian Pac J Trop Dis 2012; 2:465-470.

[27]

Ahmadi N, Safari S, Mirazi N, Karimi SA, Komaki A. Effects of vanillic acid on Aβ1-40-induced oxidative stress and learning and memory deficit in male rats. Brain Res Bull 2021; 170:264-273.

[28]

Labban S, Alghamdi BS, Alshehri FS, Kurdi M. Effects of melatonin and resveratrol on recognition memory and passive avoidance performance in a mouse model of Alzheimer’s disease. Behav Brain Res 2021; 402:1-9.

[29]

Abu-Elfotuh K, Hamdan AM, Mohamed SA, Bakr RO, Ahmed AH, Atwa AM, et al. The potential anti-Alzheimer’s activity of Oxalis corniculata Linn. methanolic extract in experimental rats: Role of APOE4/LRP1, TLR4/NF-κβ/NLRP3, Wnt 3/β-catenin/GSK-3β autophagy and apoptotic cues. J Ethnopharmacol 2024; 324:1-17.

[30]

Chaudhary G, Sharma U, Jagannathan NR, Gupta YK. Evaluation of Withania somnifera in a middle cerebral artery occlusion model of stroke in rats. Clin Exp Pharmacol Physiol Suppl 2003;( 5-6): 399-404.

[31]

Jayant S, Sharma BM, Sharma B. Protective effect of transient receptor potential vanilloid subtype 1 (TRPV1) modulator, against behavioral, biochemical and structural damage in experimental models of Alzheimer’s disease. Brain Res 2016; 1642:397-408.

[32]

Kageyama Y, Irie Y, Matsushima Y, Segawa T, Bellier JP, Hidaka K, et al. Characterization of a conformation-restricted amyloid β peptide and immunoreactivity of its antibody in human AD brain. ACS Chem Neurosci 2021; 12(18):3418-3432.

[33]

Pattanashetti LA, Patil BM, Hegde HV, Kangle RP. L.) Potential ameliorative effect of Cynodon dactylon ( pers on scopolamine-induced amnesia in rats: Restoration of cholinergic and antioxidant pathways. Indian J Pharmacol 2021; 53(1):50-59.

[34]

Mirzaee F, Hosseini A, Jouybari HB, Davoodi A, Azadbakht M. Medicinal, biological and phytochemical properties of Gentiana species. J Tradit Complement Med 2017; 7(4):400-408.

[35]

de Andrade Teles RB, Diniz TC, Costa Pinto TC, Gama e Silva M, de Lavor ÉM, et al. Flavonoids as therapeutic agents in Alzheimer’s and Parkinson’s diseases: A systematic review of preclinical evidences. Oxid Med Cell Longev 2018; 2018(1):1-21.

[36]

Wang Z, Cui X, Yan W, Liu N, Shang J, Yi X, et al. Mollugin activates GLP-1R to improve cognitive dysfunction in type 2 diabetic mice. Life Sci 2023;331. doi: 10.1016/j.lfs.2023.122026.

[37]

Ozturk Sarikaya SB. Acetylcholinesterase inhibitory potential and antioxidant properties of pyrogallol. J Enzyme Inhib Med Chem 2015; 30(5):761-766.

[38]

Chen Z, Liu Q, Zhao Z, Bai B, Sun Z, Cai L, et al. Effect of hydroxyl on antioxidant properties of 2, 3-dihydro-3, 5-dihydroxy-6-methyl-4 H-pyran-4-one to scavenge free radicals. RSC Adv 2021; 11(55):34456-34461.

[39]

Ali Reza AS, Hossain MS, Akhter S, Rahman MR, Nasrin MS, Uddin MJ, et al. In vitro antioxidant and cholinesterase inhibitory activities of Elatostema papillosum leaves and correlation with their phytochemical profiles: A study relevant to the treatment of Alzheimer’s disease. BMC Complement Altern Med 2018; 18:1-8.

[40]

Chen WN, Yeong KY. Scopolamine, a toxin-induced experimental model, used for research in Alzheimer’s disease. CNS Neurol Disord Drug Target 2020; 19(2):85-93.

[41]

Simunkova M, Alwasel SH, Alhazza IM, Jomova K, Kollar V, Rusko M, et al. Management of oxidative stress and other pathologies in Alzheimer’s disease. Arch Toxicol 2019; 93(9):2491-2513.

[42]

Marcus DL, Thomas C, Rodriguez C, Simberkoff K, Tsai JS, Strafaci JA, et al. Increased peroxidation and reduced antioxidant enzyme activity in Alzheimer’s disease. Exp Neurol 1998; 150(1):40-44.

[43]

Patel KS, Dharamsi A, Priya M, Jain S, Mandal V, Girme A, et al. Saffron (extract attenuates chronic scopolamine-induced cognitive impairment, amyloid beta, and neurofibrillary tangles accumulation in rats. J Ethnopharmacol 2024; 326:1-13.

[44]

Arya R, Jain S, Paliwal S, Madan K, Sharma S, Mishra A, et al. BACE1 inhibitors: A promising therapeutic approach for the management of Alzheimer’s disease. Asian Pac J Trop Biomed 2024; 14(9):369-381.

[45]

Barai P, Raval N, Acharya S, Acharya N. Neuroprotective effects of Bergenia ciliata on NMDA induced injury in SH-SY5Y cells and attenuation of cognitive deficits in scopolamine induced amnesia in rats. Biomed Pharmacother 2018; 108:374-390.

PDF

0

Accesses

0

Citation

Detail

Sections
Recommended

/