Scopolamine-Induced Alzheimer’s Disease in Wistar Rats: Aqueous Talinum Triangulare Potency on the Hippocampal Nissl Bodies and Long-Term Learning and Memory doi.org/10.26538/tjnpr/v6i1.19

Main Article Content

Eru M. Eru
Sadeyeng E. Anani
Samson O. Paulinus
Otu E. Mesembe
Kelechi C. Uruakpa
Nsikak M. Umoh
Michael E. Oku
Mfon I. Akpaso
Anozeng O. Igiri

Abstract

Alzheimer’s disease is a chronic neurodegenerative ailment represented clinically by studying and recalling alteration by pathologies such as intracellular neurofibrillary tangles and extracellular amyloid plaques. The study aimed at elucidating the potency of aqueous extract of Talinum triangulare leaves on the hippocampal neurons as well as assessing the long term learning and memory of scopolamine-induced Alzheimer’s type rats. Fifty-four Wistar rats (180-200 g) were used for the study; thirty rats were grouped into five groups; A, B, C, D and E while twenty-four rats were used to etablish LD50. Alzheimer’s type cognitive dysfunction was intraperitoneally (ip) induced with scopolamine hydrobromide (SHB) (1 mg/kg, ip) for seven days in groups B-E prior to the oral administration of the extract (875 and 1750 mg/kg and donepezil (1 mg/kg), followed by the Morris water maze test and histochemical staining process (Cresyl Fast Violet stains). The results revealed that the Nissl bodies were mild to moderately stained indicating protein synthesis. The enhancement of learning and memory were also seen in the treated groups compared to the untreated group. The ameliorative potentials may be attributed to the antioxidative properties of Talinum triangulare leaves which restored cells, increased protein synthesis hence, leading to enhanced learning and memory. From the above results, Talinum triangulare has ameliorative effect on the hippocampus of scopolamine-induced Alzheimer’s type cognitive dysfunction in Wistar rats. 

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How to Cite
M. Eru, E., E. Anani, S., O. Paulinus, S., E. Mesembe, O., C. Uruakpa, K., M. Umoh, N., E. Oku, M., I. Akpaso, M., & O. Igiri, A. (2022). Scopolamine-Induced Alzheimer’s Disease in Wistar Rats: Aqueous Talinum Triangulare Potency on the Hippocampal Nissl Bodies and Long-Term Learning and Memory: doi.org/10.26538/tjnpr/v6i1.19. Tropical Journal of Natural Product Research (TJNPR), 6(1), 117-122. https://tjnpr.org/index.php/home/article/view/201
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References

Agbonon A, Eklu-Gadegbeku K, Aklikokou K, Gbeassor M, Akpagana K, Tam TW, Arnason JT, Foster BC. In vitro inhibitory effect of West African medicinal and food plants on human cytochrome P450 3A subfamily. J Ethnopharm. 2010; 128(2):390-394.

Akinola OB, Omotoso OG, Dosumu OO, Akinola OS, Olutufore F. Diabetes-induced prefrontal nissl substance deficit and the effects of neem-better leaf treatment. Int J Morph. 2011; 29(3):850-856.

Bihaqi SW, Singh AP, Tiwari M. Supplementation of Convolvulus pluricaulis attenuates scopolamine-induced increased tau and Amyloid precursor protein (AßPP) expression in rat brain. Ind J Pharm. 2012; 44(5):593-598.

Buccafusco JJ. The Revival of Scopolamine Reversal for the Assessment of Cognition-Enhancing Drugs. In: Buccafusco JJ, editor. Methods of Behavior Analysis in Neuroscience (2nd ed.). Boca Raton (FL): CRC Press/Taylor and Francis. 2009; 91 p.

Cotran RS, Kumar V, Robbins S. Robbins pathologic basis of disease. (4th ed.). London: W. B. Saunders. 1989; 14-20p.

Cohen NJ and Eichenbaum H. Memory, amnesia and the hippocampal system. MIT Press, Cambridge. 1993. 326 p.

Candelario-Jalil E, Mhadu NH, Al-Dalain SM, Martinez G, Leon OS. Time course of oxidative damage in different brain regions following transient cerebral ischemia in gerbils. Neurosci Res. 2001; 41(3):233-241.

Chen KC, Baxter MG, Rodefer JS. Central blockade of muscarinic cholinergic receptors disrupts affective and attentional set-shifting. Eur J Neurosci. 2004; 20(4):1081-1088.

Citron M. Alzheimer’s disease: treatments in discovery and development. Nat Neurosci. 2002; 5(Suppl):1055-1057.

Diana RA, Yonelinas AP, Ranganath C. Medial temporal lobe activity during source retrieval reflects information type, not memory strength. J Cog Neurosci. 2010; 22(8):1808-1818.

David AO, Adelukun EA, Ayoka AO, Oluwayinka OP, Omotoso EO, Odukoya SA, Adeyemi DO. Waterleaf (talinum triangulare) enhances cerebral functions in swiss albino mice. J Neuro Sci. 2008; 25(4):239-246.

Davis RL and Robertson DM. Textbook of neuropathology. (2nd ed.). Williams and Wilkins, London. 1991; 23-26p.

Eru EM, Paulinus SO, Udo-Affah GU, Uruakpa KC, Oku ME, Anani SE, Umoh N, Akpaso MI, Anozeng OI. Hippocampal astrogliotic reduction in scopolamine hydrobromide-induced Alzheimer’s cognitive dysfunction wistar rats following administration of aqueous extract of telfairia occidentalis (Hook F.) seeds. Niger J Physiol Sci 2021; 36: 241-244.

Ekong MB, Igiri AO, Salami E, Egwu OA. Effects of artesunate on Nissl bodies of the cerebellum of wistar rats. JExp Clin Ana, 2008; 7(1):13-16.

Eru EM, Paulinus SO, Igiri AO, Akpaso MI. Enhanced Effect of Aqueous Extract of Telfairia occidentalis Seed on the Microstructure of the Hippocampus of Scopolamine Hydrobromide-Induced Cognitive Dysfunction Rats, Asian J Res Rep Neu. 2020; 3(1):5-10.

Eru EM, Paulinus SO, Udoh-Affah GU, Uruakpa KC, Oku ME, Edet UI, Igiri AO. Neurobehavioural Enhancement in Scopolamine Hydrobromide-Induced Alzheimer Type Cognitive Dysfunction in Rats Following Administration of Ethanol Seed Extract of Telfairia occidentalis (Hook.f.) Cucurbitaceae. Trop J Nat Prod Res. 2020; 4(7):282-285.

Fowler AK, Thompson J, Chen L, Dagda M, Dertien J, Dossou KSS, Kruman II. Differential Sensitivity of Prefrontal Cortex and Hippocampus to Alcohol-Induced Toxicity. PLoS ONE. 2014; 9(9):e106945.

Fenny KL, Andreanus AS, Immaculata M. Uji aktivitiesimmunostimulandaun ginseng sumatera (Talinum triangularewild) leaves and korea ginseng (panasegimseng C. A. Mayer) leaves. Banding. Indonesia. Skripsi, Department Farmasi, Institute Teknology, Banding. 1999; 189p.

Fan Y, Hu J, Li J, Yang Z, Xin X, Wang J, Ding J, Geng N. Effect of acidic oligosaccharide sugar chain on scopolamine-induced memory impairment in rats and its related mechanisms. Neurosci Lett. 2005; 374(3):222-226.

Goggin N, Rowland M, Imrie C, Walsh D, Clyne M, Drumm B. Effect of hilicobacterpylori eradication onnatural history of duodenal ulcer disease. Arch Dis Child. 1989; 79(6):502-505.

Henry G. Gray’s Anatomy; the anatomical basis of clinical practice (40th ed). Churchill Livingstone Elsevier. 2008; 225-393p.

Hasselmo ME and Eichenbaum H. Hippocampal mechanisms for the context-dependent retrieval of episodes. Neu Net. 2005; 18(9):1172-1190.

Hancianu M, Cioanca O, Mihasan M, Hritcu L. Neuroprotective effects of inhaled lavender oil on scopolamine-induced dementia via anti-oxidative activities in rats. Phytomed. 2013; 20(5):446-452.

Hoozemans JJM, Veerhuis R, Rozemuller JM,Eikelenboom P. Neuroinflammation and regeneration in the early stages of Alzheimer's disease pathology. Int J DevNeurosci. 2006; 2-3(24):157-165.

Hardy J and Selkoe DJ. The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics. Sci, 2002; 297(5580):353-356.

Hardy JA and Higgins GA. Alzheimer's disease: the amyloid cascade hypothesis. Sci, 1992; 256(5054):184-185.

Han RW, Zhang RS, Chang M, Peng YL, Wang P, Hu SQ, Choi CL, Yin M, Wang R, Han YF. Reversal of scopolamine induced spatial and recognition memory deficits in mice by novel multifunctional dimers biscognitins. Brain Res. 2012; (1470):59-68.

Jain NK, Patil CS, Kulkarni SK, Singh A. Modulatory role of cyclooxygenase inhibitors in aging- and scopolamine or lipopolysaccharide-induced cognitive dysfunction in mice. Behav Brain Res. 2002; 133(2):369-376.

Kennedy PJ and Shapiro ML. Retrieving memories via internal context requires the hippocampus. J Neurosci. 2004; 24 (31):6979-6985.

Kenneth SS. Anatomy and Physiology; the unity of form and function, third ed. McGraw Hills. United States, 2004; 539p.

Kwon SH, Ma SX, Joo HJ, Lee SY, Jang CG. Inhibitory Effects of Eucommia ulmoidesOliv. Bark on ScopolamineInduced Learning and Memory Deficits in Mice. Biomo Ther (Seoul). 2013; 21:462-469.

Kwon SH, Lee HK, Kim JA, Hong SI, Kim HC, Jo TH, Park YI, Lee CK, Kim YB, Lee SY, Jang, C. G. Neuroprotective effects of chlorogenic acid on scopolamine-induced amnesia via anti-acetylcholinesterase and anti-oxidative activities in mice. Euro J Pharm, 2010;

:210-217.

Kumar U, Dunlop DM, Richardson JS. The acute neurotoxic effect of β-amyloid on mature cultures of rat hippocampal neurons is attenuated by the anti-oxidant U-78517 F. Int J Neurosci. 1994; 79:185-190.

Koffie RM, Meyer-Luehmann M, Hashimoto T, Adams KW, Mielke ML, Garcia-Alloza M, Micheva KD, Smith SJ, Kim ML, Lee VM. Hyman, B. T., Spires-Jones, T. L. Oligomeric amyloid beta associates with postsynaptic densities and correlates with excitatory synapse loss nearsenile plaques. Proc Natl Acad Sci United States of America. 2009; 106(10):4012-4017.

Lee CH, Herman T, Clandinin TR, Lee R, Zipursky SL. Ncadherin regulates target specificity in the Drosophila visual system. Neuron. 2001; 30(2):437-450.

Lee B, Sur B, Shim J, Dae-Hyun H, Lee H. Acupuncture stimulation improves scopolamine-induced cognitive impairment via activation of cholinergic system and regulation of BDNF and CREB expressions in rats. Compl Altern Med. 2014; 14(338):1-14.

Lidner MD, Hogan JB, Hodges DB (Jr.), Orie AF, Chen P, Corsa JA, Leet JE, Gillman KW, Rose GM, Jones KM, Gribkoff BK. Donepezil primarily attenuates scopolamineinduced deficits in psychomotor function, with moderate effects on simple conditioning and attention, and small effects on working memory and spatial mapping. Psychopharm (Berl), 2006; 188:629-640.

Lorke D. A new approach to practical acute toxicity testing. Arch Toxicol. 1983; 54(4):275-287.

Mohamed T and Rao PPN. Alzheimer’s disease: Emerging trends in small molecule therapies. Curr Med Chem. 2011; 18(28):4299-4320.

Morris RGM, Garrud P, Rawlins JN, O'Keefe J. Place navigation impaired in rats with hippocampal lesions. Nature. 1982; 297(5868):681-683.

Nitta A, Katono Y, Itoh A, Hasegawa T, Nabeshima T. Nicotine reverse scopolamine-induced impairment of performance in passive avoidance task in rats through its action on the dopaminergic neuronal system. PharmBiochem Behav. 1994; 49(4):807-812.

Oh JH, Choi BJ, Chang MS, Park KS. Nelumbo nucifera semen extract improves memory in rats with scopolamineinduced amnesia through the induction of choline acetylcholinesterase expression. Neurosci Lett. 2009;55(1):41-44.

Ofusor DA, Adelakun AE, Ayoka AO, Oluwayinka OP, Omotoso EO, Odukossya SA, Adeyemi DO. Water leaf (Talinum triangulare) enhances cerebral functions in Swiss albino mice. J Neurol Sci. 2008; 25:239-246.

Preston AR and Eichenbaum H. Interplay of hippocampus and prefrontal cortex in memory. Curr Bio.2013; 23(17):764-773.

Parle M, Dhingra D, Kulkarni SK. Neuromodulators of learning and memory. Asian Pac J Pharm. 2004; 16:89-99.

Perry G, Cash AD, Smith MA. Alzheimer disease and oxidative stress. J Biomed Biotech. 2002; 2:120-123.

Pharm-Huy LA, He H, Phar-Huy C. Free radical. Antioxidants in disease and health. Int J Biomed Sci. 2008; 4(2):89-96.

Prince M, Bryce R, Ferri C. World Alzheimer Report 2011: The benefits of early diagnosis and intervention. Available from: www.alz.co.uk/worldreport2011. Accessed 15th May 2019.

Rabiei Z, Mokhtari S, Asgharzade S, Gholami M, Rahnama S, Rafieian-Kopaei M. Inhibitory effect of thymus vulgaris extract on memory impairment induced by scopolamine in rat. Asian Pacific J Trop Biomed. 2015; 5(10):845-851.

Rabiei Z, Hojjati M, Rafieian-Kopaeia M, Alibabaei Z. Effect of cyperusrotudusethanolic extract on learning and memory in animal model of Alzheimer. Biomed Aging Pathol. 2013; 3(4):185-191.

Rod RS, Trent DS, Philip T. Anatomy and Physiology. (8thed.) McGraw Hills. United States, 2008; 503p.

Rubio J, Dang H, Gong M, Liu X, Chen SL, Gonzales GF. Aqueous and hydroalcoholic extract of black maca (Lepidium meyenii) improve scopolamine-induced memory impairment in mice. Food Chem Toxicol. 2007; 45(10):1882-1890.

Rubio J, Yucra S, Gasco M, Gonzales GF. Dose-response effect of black maca (Lepidium meyenii) in mice with memory impairment induced by ethanol. Toxicol MechMet. 2011; 21(8):628-634.

Sadeyeng EA, Eru EM, Okon DE, Uruakpa KC, Ugbem TI, Igiri AO. The effect of averrhoa carambola (star fruit)aqueous fruit extract on hippocampal astrocyte expression following diazepam-induced neurotoxicity in wistar rats. Trop J Nat Prod Res 2020; 4(12): 1170-1173.

Suh WH, Suslick KS, Suh YH. Therapeutic agents for Alzheimer’s disease. Cent Ner Sys Agents Med Chem. 2005; 5(4):259-269.

Sutherland RJ, Whishaw IQ, Kolb B. A behavioural analysis of spatial localization following electrolytic, kainite or colchicine-induced damage to the hippocampal formation in rats. Behav Brain Res. 1983; 7(2):133-153.

Saija A, Scalese M, Lauza M, Narzullo D, Bonina F, Castelli F. Flavonoids as antioxidant agents: importance of their interaction with biomembranes. Free Rad Bio Med. 1995; 19(4):481-486.

Terry AV (Jr.). Muscarinic Receptor Antagonists in Rats. In: Levin ED, Buccafusco JJ, editors. Animal Models of Cognitive Impairment. Boca Raton, (Florida): CRCPress/Taylor and Francis. 2006; 59p. Available from: https://pubmed.ncbi.nlm.nih.gov/21204367. accessed

/06/2019

Tota S, Nath C, Najmi AK, Shukla R, Hanif K. Inhibition of central angiotensin converting enzyme ameliorates scopolamine induced memory impairment in mice: role of cholinergic neurotransmission, cerebral blood flow and brain energy metabolism. Behav Brain Res. 2012; 232(1):66-76.

Tsukada H, Kakiuchi T, Ando I, Ouchi Y. Functional activation of cerebral blood flow abolished by scopolamine is reversed by cognitive enhancers associated with cholinesterase inhibition: a positron emission tomography study in unanesthetized monkeys. J Pharm Exp Ther. 1997; 281(3):1408-1414.

Tromfimiuk E, Walesiuk A, Braszko JJ. St. John’s wort (Hypenicumperforatum) diminishes cognitive impairment caused by the chronic restraint stress in rats. PharmacolRes. 2005; 51(3):239-246.

Williams P, Sorribas A, Howes MJ. Natural products as a source of Alzheimer’s drug leads. Nat Prod Rep. 2011; 28(1):48-77.

Yágüez L, Shaw KN, Morris R, Matthews D. The effects on cognitive functions of a movement-based intervention in patients with Alzheimer's type dementia: a pilot study. Int JGer Psy, 2010; 26(2):173-181.

Zheng SQ, PalovcakE, Armache JP, Verba KA, Cheng Y, Agard DA. MotionCor2: anisotropic correction of beaminduced motion for improved cryo-electron microscopy. Nat Met. 2017; 14 (4):331-332.