期刊论文详细信息
BMC Complementary and Alternative Medicine
Memory-enhancing activities of the aqueous extract of Albizia adianthifolia leaves in the 6-hydroxydopamine-lesion rodent model of Parkinson’s disease
Lucian Hritcu6  Théophile Dimo4  Monica Hancianu5  Oana Cioanca5  Zenovia Olteanu6  Nolé Tsabang3  Harquin Simplice Foyet1  Alain Bertrand Dongmo2  Galba Jean Beppe1 
[1] Department of Agriculture, Cattle farming and Derived products, High Institute of the Sahel, University of Maroua, Maroua, Cameroon;Department of Animal Biology and Physiology, University of Douala, Douala, Cameroon;Centre for Research on Medicinal Plants and Traditional Medicine, Institute of Medical Research and Medicinal Plant Studies, Yaoundé, Cameroon;Laboratory of Animal Physiology, University of Yaoundé I, Yaounde, Cameroon;Faculty of Pharmacy, University of Medicine and Pharmacy “Gr. T. Popa”, Iasi, Romania;Department of Biology, Alexandru Ioan Cuza University, Iasi, Romania
关键词: Parkinson disease;    Memory;    6-hydroxydopamine-lesion rat;    Antioxidant activity;    Albizia adianthifolia extract;   
Others  :  1220181
DOI  :  10.1186/1472-6882-14-142
 received in 2013-10-07, accepted in 2014-04-25,  发布年份 2014
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【 摘 要 】

Background

Albizia adianthifolia (Schumach.) W. Wright (Fabaceae) is a traditional herb largely used in the African traditional medicine as analgesic, purgative, anti-inflammatory, antioxidant, antimicrobial and memory-enhancer drug. This study was undertaken in order to evaluate the possible cognitive-enhancing and antioxidative effects of the aqueous extract of A. adianthifolia leaves in the 6-hydroxydopamine-lesion rodent model of Parkinson’s disease.

Methods

The effect of the aqueous extract of A. adianthifolia leaves (150 and 300 mg/kg, orally, daily, for 21 days) on spatial memory performance was assessed using Y-maze and radial arm-maze tasks, as animal models of spatial memory. Pergolide - induced rotational behavior test was employed to validate unilateral damage to dopamine nigrostriatal neurons. Also, in vitro antioxidant activity was assessed through the estimation of total flavonoid and total phenolic contents along with determination of free radical scavenging activity. Statistical analyses were performed using two-way analysis of variance (ANOVA). Significant differences were determined by Tukey’s post hoc test. F values for which p < 0.05 were regarded as statistically significant. Pearson’s correlation coefficient and regression analysis were used in order to evaluate the association between behavioral parameters and net rotations in rotational behavior test.

Results

The 6-OHDA-treated rats exhibited the following: decrease of spontaneous alternations percentage within Y-maze task and increase of working memory errors and reference memory errors within radial arm maze task. Administration of the aqueous extract of A. adianthifolia leaves significantly improved these parameters, suggesting positive effects on spatial memory formation. Also, the aqueous extract of A. adianthifolia leaves showed potent in vitro antioxidant activity. Furthermore, in vivo evaluation, the aqueous extract of A. adianthifolia leaves attenuated the contralateral rotational asymmetry observed by pergolide challenge in 6-OHDA-treated rats.

Conclusions

Taken together, our results suggest that the aqueous extract of A. adianthifolia leaves possesses antioxidant potential and might provide an opportunity for management neurological abnormalities in Parkinson’s disease conditions.

【 授权许可】

   
2014 Beppe et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Choi JG, Kim HG, Kim MC, Yang WM, Huh Y, Kim SY, Oh MS: Polygalae radix inhibits toxin-induced neuronal death in the Parkinson's disease models. J Ethnopharmacol 2011, 134(2):414-421.
  • [2]Dick FD, De Palma G, Ahmadi A, Scott NW, Prescott GJ, Bennett J, Semple S, Dick S, Counsell C, Mozzoni P, Haites N, Wettinger SB, Mutti A, Otelea M, Seaton A, Soderkvist P, Felice A: Environmental risk factors for Parkinson’s disease and parkinsonism: the Geoparkinson study. Occup Environ Med 2007, 64:666-672.
  • [3]Foyet HS, Hritcu L, Ciobica A, Stefan M, Kamtchouing P, Cojocaru D: Methanolic extract of Hibiscus asper leaves improves spatial memory deficits in the 6-hydroxydopamine-lesion rodent model of Parkinson's disease. J Ethnopharmacol 2011, 133:773-779.
  • [4]Meissner WG, Frasier M, Gasser T, Goetz CG, Lozano A, Piccini P, Obeso JA, Rascol O, Schapira A, Voon V, Weiner DM, Tison F, Bezard E: Priorities in Parkinson's disease research. Nat Rev Drug Discov 2011, 10(5):377-393.
  • [5]Fukae J, Mizuno Y, Hattori N: Mitochondrial dysfunction in parkinson’s disease. Mitochondrion 2007, 7(1–2):58-62.
  • [6]Henchcliffe C, Beal MF: Mitochondrial biology and oxidative stress in parkinson’s disease pathogenesis. Nat Clin Pract Neurol 2008, 4:600-609.
  • [7]Zhou C, Huang Y, Przedborski S: Oxidative stress in parkinson's disease: a mechanism of pathogenic and therapeutic significance. Ann N Y Acad Sci 2008, 1147:93-104.
  • [8]Moreira EG, Rial D, Aguiar A Jr, Figueiredo C, Siqueira J, DalBó S, Horst H, Oliveira J, Mancini G, dos Santos T, Villarinho J, Pinheiro F, Marino-Neto J, Ferreira J, Bem A, Latini A, Pizzolatti M, Ribeiro-do-Valle R, Prediger RS: Proanthocyanidin-rich fraction from Croton celtidifolius Baill confers neuroprotection in the intranasal 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine rat model of Parkinson’s disease. J Neural Transm 2010, 117(12):1337-1351.
  • [9]Myung SY, Hibiki K, Dae JK, Hong SC, Jin HS: Experimental strategy to identify genes susceptible to oxidative stress in nigral dopaminergic neurons. Neurochem Res 2004, 29:1223-1234.
  • [10]Song J-X, Sze SC-W, Ng T-B, Lee CK-F, Leung GPH, Shaw P-C, Tong Y, Zhang Y-B: Anti-parkinsonian drug discovery from herbal medicines: what have we got from neurotoxic models? J Ethnopharmacol 2012, 139(3):698-711.
  • [11]Cannon JR, Greenamyre JT: Neurotoxic in vivo models of parkinson’s disease recent advances. Prog Brain Res 2010, 184:17-33.
  • [12]Beal MF: Experimental models of parkinson’s disease. Nat Rev Neurosci 2001, 2:325-334.
  • [13]Blum D, Torch S, Lambeng N, Nissou M, Benabid AL, Sadoul R, Verna JM: Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson’s disease. Prog Neurobiol 2001, 65:135-172.
  • [14]Singh S, Dikshit M: Apoptotic neuronal death in Parkinson’s disease: involvement of nitric oxide. Brain Res Rev 2007, 54:233-250.
  • [15]Fox SH, Brotchie JM: The MPTP-lesioned non-human primate models of Parkinson’s disease. Past, present, and future. Prog Brain Res 2010, 184:133-157.
  • [16]Houghton PJ, Howes MJ: Natural products and derivatives affecting neurotransmission relevant to Alzheimer’s and Parkinson’s disease. Neurosignals 2005, 14:6-22.
  • [17]Hritcu L, Foyet HS, Stefan M, Mihasan M, Asongalem AE, Kamtchouing P: Neuroprotective effect of the methanolic extract of Hibiscus asper leaves in 6-hydroxydopamine-lesioned rat model of Parkinson's disease. J Ethnopharmacol 2011, 137(1):585-591.
  • [18]Todorov IN, Zaikov GE, Degterev IA: Bioactive compounds: biotransformation of biological action, mechanism of antistress and anabolic action of Eleutherococcus. Commack, New York: Nova Science Publishers, Inc.; 1993.
  • [19]Van Wyk B-E, Gericke N: People’s Plants: A guide to useful plants of Southern Africa. Pretoria: Briza Publications; 2000.
  • [20]Watt JM, Breyer-Brandwyk MG: The medicinal and poisonous plants of Southern and Easthern Africa. 2nd edition. E&S Livingstone LTD: Edinburgh and London; 1962.
  • [21]Stafford GI, Pedersen ME, Van Staden J, Jäger AK: Review on plants with CNS-effects used in traditional South African medicine against mental diseases. J Ethnopharmacol 2008, 119(3):513-537.
  • [22]Haddad M, Miyamoto T, Laurens V, Lacaille-Dubois MA: Two new biologically active triterpenoidal saponins acylated with salicylic acid from Albizia adianthifolia. J Nat Prod 2003, 66:372-377.
  • [23]Kim WK, Jung JW, Ahn NY, Oh HR, Lee BK, Oh JK, Cheong JH, Chun HS, Ryu JH: Anxiolytic-like effects of extracts from Albizzia julibrissin bark in the elevated plus-maze in rats. Life Sci 2004, 75:2787-2795.
  • [24]Jung Y-H, Ha R-R, Kwon S-H, Hong S-I, Lee K-H, Kim S-Y, Lee S-Y, Jang C-G: Anxiolytic effects of Julibroside C1 isolated from Albizzia julibrissin in mice. Prog Neuro-Psychoph 2013, 44:184-192.
  • [25]Kokila K, Priyadharshini S, Sujatha V: Phytopharmacological properties of albizia species: a review. Int J Pharm Pharm Sci 2013, 5:70-73.
  • [26]Chang CC, Yang MH, Wen MH, Chern JC: Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal 2002, 10:178-182.
  • [27]Singleton VL, Rossi JA: Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagent. Am J Enol Viticult 1965, 16:144-158.
  • [28]Seal T: Antioxidant activity of some wild edible plants of Meghalaya state of India: A comparison using two solvent extraction systems. 2012, 4:51-56.
  • [29]Paxinos G, Watson C: The Rat Brain in Stereotaxic Coordinates. Elsevier, San Diego: Academic Press; 2005.
  • [30]Franklin AE, Engeland CG, Kavaliers M, Ossenkopp K-P: Lipopolysaccharide-induced hypoactivity and behavioral tolerance development are modulated by the light–dark cycle in male and female rats. Psychopharmacology 2003, 170:399-408.
  • [31]Fuller R, Clemens J: Pergolide: a dopamine agonist at both D1 and D2 receptors. Life Sci 1991, 49:925-930.
  • [32]Herrera-Marschitz M, Arbuthnott G, Ungerstedt U: The rotational model and microdialysis: Significance for dopamine signalling, clinical studies, and beyond. Prog Neurobiol 2010, 90:176-189.
  • [33]Rajendra Kopalli S, Koppula S, Young Shin K, Noh S-J, Jin Q, Yeon Hwang B, Suh Y-H: SF-6 attenuates 6-hydroxydopamine-induced neurotoxicity: An in vitro and in vivo investigation in experimental models of Parkinson's disease. J Ethnopharmacol 2012, 143(2):686-694.
  • [34]Jackson LL: V.T.E. on an elevated maze. J Comp Psychol 1943, 36:99-107.
  • [35]Hritcu L, Cioanca O, Hancianu M: Effects of lavender oil inhalation on improving scopolamine-induced spatial memory impairment in laboratory rats. Phytomedicine 2012, 19(6):529-534.
  • [36]Olton DS, Samuelson RJ: Remembrance of places passed: Spatial memory in rats. J Exp Psychol Anim B 1976, 2:97-116.
  • [37]Wang X, Hai CX, Liang X, Yu SX, Zhang W, Li YL: The protective effects of Acanthopanax senticosus Harms aqueous extracts against oxidative stress: Role of Nrf2 and antioxidant enzymes. J Ethnopharmacol 2010, 127(2):424-432.
  • [38]Mabogo DEN: The Ethnobotany of the Vhavenda. MSc thesis: University of Pretoria; 1990.
  • [39]Tamokou J, Simo Mpetga D, Keilah Lunga P, Tene M, Tane P, Kuiate J: Antioxidant and antimicrobial activities of ethyl acetate extract, fractions and compounds from stem bark of Albizia adianthifolia (Mimosoideae). BMC Complement Altern Med 2012, 12(1):99. BioMed Central Full Text
  • [40]Hall CA, Cuppett SL: Structure activities of natural antioxidants. In Antioxidant methodology in vitro concepts. Edited by Hudson BJL. London: Elsevier Applied Science; 1997:1-18.
  • [41]Pietta P, Sionetti P, Mauri P: Antioxidant activity of selected medicinal plants. J Agric Food Chem 1998, 46:4487-4490.
  • [42]Good M: Spatial memory and hippocampal function: where are we now? Psicológica 2002, 23:109-138.
  • [43]Winnicka MM, Wisniewski K: Bilateral 6-OHDA lesions to the hippocampus attenuate the facilitatory effect of CCK-8US and caerulein on memory in rats. Pharmacol Res 2000, 41:347-353.
  • [44]Kandel ER: The molecular biology of memory storage: A dialogue between genes and synapses. Science 2001, 294(5544):1030-1038.
  • [45]Hritcu L, Ciobica A, Artenie V: Effects of right-unilateral 6-hydroxydopamine infusion-induced memory impairment and oxidative stress: relevance for Parkinson’s disease. Cent Eur J Biol 2008, 3:250-257.
  • [46]Sriraksa N, Wattanathorn J, Muchimapura S, Tiamkao S, Brown K, Chaisiwamongkol K: Cognitive-enhancing effect of quercetin in a rat model of Parkinson's disease induced by 6-Hydroxydopamine. Evid Based Complement Alternat Med 2012, 2012:9. Article ID 823206
  • [47]Taupin P: Apigenin and related compounds stimulate adult neurogenesis. Expert Opin Ther Pat 2009, 19(4):523-527.
  • [48]Yusuf S, Adelaiye BA, Agunu A: Effect of Ziziphus mauritiania (L.) seed extracts on spatial recognition memory of rats as measured by the Y-maze test. J Nat Prod 2009, 2:31-39.
  • [49]Bagheri M, Joghataei M-T, Mohseni S, Roghani M: Genistein ameliorates learning and memory deficits in amyloid β(1–40) rat model of Alzheimer’s disease. Neurobiol Learn Mem 2011, 95(3):270-276.
  • [50]Mizuno M, Yamada K, Olariu A, Nawa H, Nabeshima T: Involvement of brain-derived neurotrophic factor in spatial memory formation and maintenance in a radial arm maze test in rats. J Neurosci 2000, 20(18):7116-7121.
  • [51]Titus ADJ, Shankaranarayana BS, Harsha HN, Ramkumar K, Srikumar BN, Singh SB, Chattarji S, Raju TR: Hypobaric hypoxia-induced dendritic atrophy of hippocampal neurons is associated with cognitive impairment in adult rats. Neuroscience 2007, 145:265-278.
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