Reversal effect of Solanum dasyphyllum against rotenone-induced neurotoxicity

1. Park SE, Sapkota K, Choi JH. et al. Rutin from Dendropanax morbifera Leveille protects human dopaminergic cells against rotenone-induced cell injury through inhibiting JNK and p38 MAPK signaling. Neurochem Res. 2014;39(4):707–18.10.1007/s11064-014-1259-5 Search in Google Scholar

2. Hisahara S, Shimohama S. Toxin-induced and genetic animal models of Parkinson’s disease. Parkinsons Dis. 2011;2011:9517–9.10.4061/2011/951709 Search in Google Scholar

3. Enogieru AB, Haylett W, Hiss DC, Bardien S, Ekpo OE. Rutin as a potent antioxidant: implications for neurodegenerative disorders. Oxi Med Cell Longev. 2018;ID 6241017:1–17.10.1155/2018/6241017 Search in Google Scholar

4. Doughari JH. Phytochemicals: Extraction methods, basic structures and mode of action as potential chemotherapeutic agents, phytochemicals – A global perspective of their role in nutrition and health. [http://www.intechopen.com/books/phytochemicalsa-global-perspective-of-their-role-in-nutrition-andhealth/phytochemicals-extractionmethods-basic-structures-and-mode-of-action-as-potentialchemotherapeutic] Search in Google Scholar

5. Renaud J, Martinol M. Resveratrol as a protective molecule for neuroinflammation: A review of mechanisms. Curr Pharm Biotechnol. 2014;15:1–12.10.2174/1389201015666140617101332 Search in Google Scholar

6. Adesina SK. Constituents of Solanum Dasyphyllum fruit. J Nat Prod. 1985;48(1):147.10.1021/np50037a033 Search in Google Scholar

7. Ali Z, Xu ZL; Zhang DY, He XL, Bahadur L, Yi XY. Molecular diversity analysis of eggplant (Solanum melongena) genetic resources. Genet Mol Res. 2013;10(2):1141–55.10.4238/vol10-2gmr1279 Search in Google Scholar

8. Ajayi IA, Ojelere O. Evaluation of the antimicrobial properties of the ethanolic extracts of some medicinal plant Seeds from South-West Nigeria. IOSR-JPBS. 2014;9(4):80–5.10.9790/3008-09418085 Search in Google Scholar

9. Coune C, Denoel A. Etude phytochimique des solanaceae d’afrique centrale i. Les alcalo~deds e Solanum dasyphyllum. Planta Med. 1975;28:168–71.10.1055/s-0028-1097846 Search in Google Scholar

10. Puy velde LV, Geysen D, Ayobangira F, Nakizamungu E, Nswimiyimana A, Kalisa A. screening of medicinal plants of Rwanda for Acaricidal activity. J Ethnopharmacol. 1985;13:209–15.10.1016/0378-8741(85)90008-X Search in Google Scholar

11. Clementino-Neto J, Pereira JC, Vasconcelos LHC, de Souza ILL, Silva ADS, Silva TMG, et al. Toxicological, Antidiarrheal, and Spasmolytic Activities of Solanum paniculatum. Planta Med. 2016; 82:58–64. Search in Google Scholar

12. Obade E, Ilesanmi OB, Crown O, Akinmoladun AC, Olaleye MT, Akindahunsi AA. Neuromodulatory effect of solvent fractions of Africa eggplant (Solanum dadyphyllum) against KCN-induced mitochondria damage, viz. NADH-succinate dehydrogenase, NADH- cytochrome c reductase, and succinate-cytochrome c reductase. Clin Phytosci. 2018;4(9):1–9. Search in Google Scholar

13. Li X, He G, Mu X, Xu B, Tian S, Yu X, et al. Protective effects of baicalein against rotenone-induced neurotoxicity in PC12 cells and isolated rat brain mitochondria. Eur J Pharmacol. 2012;674:227–33.10.1016/j.ejphar.2011.09.18121996316 Search in Google Scholar

14. Sherer TB, Betarbet R, Testa CM, Seo BB, Richardson JR, Kim JH, et al. Mechanism of toxicity in rotenone models of Parkinson’s disease. J Neurosci. 2003;23(34):10756–64.10.1523/JNEUROSCI.23-34-10756.2003 Search in Google Scholar

15. Swarnkar S, Tyagi E, Agrawal R, Singh MP, Nath C. A comparative study on oxidative stress induced by LPS and rotenone in homogenates of rat brain regions. ETAP. 2009;27:219–24.10.1016/j.etap.2008.10.003 Search in Google Scholar

16. Okhawa H. Assay for lipid peroxide in animal tissues by Thiobarbituric acid reaction. Annu Rev Biochem. 1979;95:351–2.10.1016/0003-2697(79)90738-3 Search in Google Scholar

17. Levine RL, Garland D, Oliver C, Amici A, Climent I, Lenz A. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol. 1990;186:464–78.10.1016/0076-6879(90)86141-H Search in Google Scholar

18. Ellman GL, Courtney KD, Andres V, Feather-Stone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7:88–95.10.1016/0006-2952(61)90145-9 Search in Google Scholar

19. Spinazzi M, Casarin A, Pertegato V, Salviati L, Angelini C. Assessment of mitochondrial respiratory chain enzymatic activities on tissues and cultured cells. Nat Protoc. 2012;7(6):1235–46.10.1038/nprot.2012.05822653162 Search in Google Scholar

20. Kollareth DMJ, Muralidhara M. Neuroprotective efficacy of a combination of Fish oil and Ferulic acid against 3-nitropropionic acid-induced oxidative stress and neurotoxicity in rats: behavioral and biochemical evidence. APNM. 2003;39(4):1–10. Search in Google Scholar

21. Kchaou W, Abbès F, Blecker C, Attia H, Besbes S. 2013. Effects of extraction solvents on phenolic contents and antioxidant activities of Tunisian date varieties (Phoenix dactylifera L.). Industrial Crops Products. 2013;45:262–9.10.1016/j.indcrop.2012.12.028 Search in Google Scholar

22. Ngo TV, Scarlett CJ, Bowyer MC, Ngo PD, Vuong QV. Impact of different extraction solvents on bioactive compounds and antioxidant capacity from the root of Salacia chinensis L. J Food Qual. 2017;1:1–8.10.1155/2017/9305047 Search in Google Scholar

23. Belwal T, Ezzat SM, Rastrelli L, Bhatt ID, Daglia M, Baldi A, et al. A critical analysis of extraction techniques used for botanicals: trends, priorities, industrial uses, and optimization strategies. TrAC. 2018;100:82–102.10.1016/j.trac.2017.12.018 Search in Google Scholar

24. Dirar AI, Alsaadi DHM, Wada M, Mohamed MA, Watanabe T, Devkota HP. 2019. Effects of extraction solvents on total phenolic and flavonoid contents and biological activities of extracts from Sudanese medicinal plants. S Afr J Bot. 2019;120:261–7.10.1016/j.sajb.2018.07.003 Search in Google Scholar

25. Roddick JG. Steroidal glycoalkaloid nature and sequences of bioactivity. Adv Exp Med Biol. 1996;404:277–95.10.1007/978-1-4899-1367-8_25 Search in Google Scholar

26. Roddick JG, Weissenberg M, Leonard AL. Membrane disruption and enzyme inhibition by naturally-occurring and modified chacotriose-containing Solanum steroidal glycoalkaloids. Phytochemistry. 2001; 56(6):603–10.10.1016/S0031-9422(00)00420-9 Search in Google Scholar

27. Tai BH, Doan VV, Pham Yen PH, Nhiem NX, Cuc NT, Trang DT, et al. Two new steroidal alkaloid saponins from the whole plants of Solanum nigrum. NPC. 2018;13(11):1457–60.10.1177/1934578X1801301111 Search in Google Scholar

28. Shela MK, Patil MJ, Bhujbal SS, Chaudhari RB. Evaluation of the anticonvulsant activity of the ethanolic extracts from leaves of Excoecaria agallocha. FJPS. 2018;4(2):215–9. Search in Google Scholar

29. Velmurugan BK, Rathinasamy B, Lohanathan BP, Thiyagarajan V, Weng C. Neuroprotective role of phytochemicals. Molecules. 2018; 23(2485):1–15.10.3390/molecules23102485622249930262792 Search in Google Scholar

30. Muralidhara GK. (2013) Neuroprotective effects of tomato seed extract against rotenone-induced oxidative impairments and neurotoxicity in mice. Toxicol Lett. 2013;221(Suppl.):S237. Search in Google Scholar

31. Sudati JH, Vieira FA, Pavin SS, Mundstock D, Seeger RL, Golombieski R, et al. Valeriana officinalis attenuates the rotenone-induced toxicity in Drosophila melanogaster. Neurotoxicology. 2013;37:118–26.10.1016/j.neuro.2013.04.00623639798 Search in Google Scholar

32. Thakur P, Nehru B. Long-term heat shock proteins (HSPs) induction by carbenoxolone improves hallmark features of Parkinson’s disease in a rotenone-based model. Neuropharmacol. 2013;79C:190–200.10.1016/j.neuropharm.2013.11.01624296154 Search in Google Scholar

33. Betarbet R, Canet-Aviles RM, Sherer TB, Mastroberardino PG, McLendon C, Kim JH, et al. Intersecting pathways to neurodegeneration in Parkinson’s disease: effects of the pesticide rotenone on DJ-1, alpha-synuclein, and the ubiquitin-proteasome system. Neurobiol Dis. 2006;22(2):404–20.10.1016/j.nbd.2005.12.00316439141 Search in Google Scholar

34. Joseph D, Muralidhara KM. Enhanced neuroprotective effect of fish oil in combination with quercetin against3-nitropropionic acid-induced oxidative stress in rat brain. Prog Neuro-Psychopharmacol Biol Psychiatry. 2013;40:83–92.10.1016/j.pnpbp.2012.08.01822960609 Search in Google Scholar

35. Muralidhara CG. Neuroprotective effect of aqueous extract of Selaginella delicatula as evidenced by abrogation of rotenone-induced motor deficits, oxidative dysfunctions, and neurotoxicity in mice. Cell Mol Neurobiol. 2013;33:929–42.10.1007/s10571-013-9959-y23868340 Search in Google Scholar

36. Yankuzo HM, Baraya YS, Mustapha Z, Wong KK, Yaacob NS. Immunomodulatory effects of a bioactive fraction of Strobilanthes crispus in NMU-induced rat mammar y tumor model. J Ethnopharmacol. 2018;213:31–7.10.1016/j.jep.2017.10.02429100935 Search in Google Scholar

37. Liu Z, Zhou T, Ziegler AC, Dimitrion P, Zuo L. Oxidative stress in neurodegenerative diseases: From molecular mechanisms to clinical applications. Oxi Med Cell Longev. 2017;ID 2525967:1–11.10.1155/2017/2525967552966428785371 Search in Google Scholar

38. Moreira PI, Zhu X, Wang X, Lee H, Nunomuro A, Petersen RB, et al. Mitochondria: a therapeutic target in neurodegeneration. BBA. 2010;1802:212–20.10.1016/j.bbadis.2009.10.007279054019853657 Search in Google Scholar

39. Ilesanmi OB, Akinmoladun AC, Olayeriju OS, Saliu IO, Olaleye MT, Akindahunsi AA. Modulation of key biochemical markers relevant to stroke by Antiaris africana leaf extract following cerebral ischemia/reperfusion injury. Afr J Tradit Complement Altern Med. 2017;14(4):253–64.10.21010/ajtcam.v14i4.28547147328638888 Search in Google Scholar

40. Pandey S, Singh B, Khan MMAA, Mahdi AA. Pharmacological profile of Bacopa monnieri: An approach to prevention and treatment of diseases. Herb Med Mod Drug Discovery. 2017;189–204. Search in Google Scholar

41. Sandler M, Glover S. Neurotoxins and monoamine oxidase B inhibitors: possible mechanisms for the neuroprotective effect of (y¨) deprenyl. Inhibitors of Monoamine Oxidase B.1993:169–81.10.1007/978-3-0348-6348-3_8 Search in Google Scholar

42. Dalle-Donne I, Scaloni A, Giustarini D, Cavarra E, Tell G, Lungarella G, Colombo R, et al. 2005. Proteins as biomarkers of oxidative/nitrosative stress in diseases: the contribution of redox proteomics. Mass Spectrom Rev. 2005;24:55–99.10.1002/mas.2000615389864 Search in Google Scholar