PMID- 33489038 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220420 IS - 2008-3866 (Print) IS - 2008-3874 (Electronic) IS - 2008-3866 (Linking) VI - 23 IP - 12 DP - 2020 Dec TI - Bee venom attenuates neurodegeneration and motor impairment and modulates the response to L-dopa or rasagiline in a mice model of Parkinson's disease. PG - 1628-1638 LID - 10.22038/ijbms.2020.46469.10731 [doi] AB - OBJECTIVES: This study aimed to investigate the effect of bee venom, a form of alternative therapy, on rotenone-induced Parkinson's disease (PD) in mice. Moreover, the possible modulation by bee venom of the effect of L-dopa/carbidopa or rasagiline was examined. MATERIALS AND METHODS: Rotenone (1.5 mg/kg, subcutaneously; SC) was administered every other day for two weeks and at the same time mice received the vehicle (DMSO, SC), bee venom (0.065, 0.13, and 0.26 mg/kg; intradermal; ID), L-dopa/carbidopa (25 mg/kg, intraperitoneal; IP), L-dopa/carbidopa+bee venom (0.13 mg/kg, ID), rasagiline (1 mg/kg, IP) or rasagiline+bee venom (0.13 mg/kg, ID). Then, wire hanging and staircase tests were performed and mice were euthanized and brains' striata separated. Oxidative stress biomarkers namely, malondialdehyde (MDA), nitric oxide (NO), reduced glutathione (GSH), paraoxonase-1 (PON-1), and total antioxidant capacity (TAC) were measured. Additionally, butyrylcholinesterase (BuChE), monocyte chemoattractant protein-1 (MCP-1), tumor necrosis factor-alpha (TNF-alpha), and dopamine (DA) were evaluated. Brain histopathological changes and caspase-3- expression were done. RESULTS: Bee venom significantly enhanced motor performance and inhibited rotenone-induced oxidative/nitrosative stress, observed as a reduction in both MDA and NO along with increasing GSH, PON-1, and TAC. Besides, bee venom decreased MCP-1, TNF-alpha, and caspase-3 expression together with an increase in BuChE activity and DA content. CONCLUSION: Bee venom alone or in combination with L-dopa/carbidopa or rasagiline alleviated neuronal degeneration compared with L-dopa/carbidopa or rasagiline treatment only. Bee venom via its antioxidant and cytokine reducing potentials might be of value either alone or as adjunctive therapy in the management of PD. FAU - Badawi, Hanaa Mm AU - Badawi HM AD - Holding Company for Biological Products, Vaccines and Drugs (VACSERA), Cairo, Egypt. FAU - Abdelsalam, Rania M AU - Abdelsalam RM AD - Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt. FAU - Abdel-Salam, Omar Me AU - Abdel-Salam OM AD - Department of Toxicology and Narcotics, National Research Centre, Cairo, Egypt. FAU - Youness, Eman R AU - Youness ER AD - Department of Medical Biochemistry, National Research Centre, Cairo, Egypt. FAU - Shaffie, Nermeen M AU - Shaffie NM AD - Department of Pathology, National Research Centre, Cairo, Egypt. FAU - Eldenshary, Ezz-El Din S AU - Eldenshary EDS AD - Department of Pharmacology and Toxicology, Faculty of Pharmacy, Cairo University, Cairo, Egypt. LA - eng PT - Journal Article PL - Iran TA - Iran J Basic Med Sci JT - Iranian journal of basic medical sciences JID - 101517966 PMC - PMC7811814 OTO - NOTNLM OT - Bee venom OT - Dopamine OT - Oxidative stress OT - Parkinson's disease OT - Rotenone EDAT- 2021/01/26 06:00 MHDA- 2021/01/26 06:01 PMCR- 2020/12/01 CRDT- 2021/01/25 05:40 PHST- 2021/01/25 05:40 [entrez] PHST- 2021/01/26 06:00 [pubmed] PHST- 2021/01/26 06:01 [medline] PHST- 2020/12/01 00:00 [pmc-release] AID - 10.22038/ijbms.2020.46469.10731 [doi] PST - ppublish SO - Iran J Basic Med Sci. 2020 Dec;23(12):1628-1638. doi: 10.22038/ijbms.2020.46469.10731.