Coenzyme Q10 attenuates neurodegeneration in the cerebellum induced by chronic exposure to tramadol

被引:0
|
作者
Keyhanifard, Majid [1 ,2 ,3 ]
Javan, Roghayeh [4 ]
Disfani, Reza Ataee [5 ]
Bahrami, Maryam [6 ]
Mirzaie, Mohamad Sedigh [7 ]
Taghiloo, Saeid [8 ]
Mokhtari, Hossein [9 ]
Nasiry, Davood [9 ]
Aghajani, Zahra Sadrzadeh [10 ]
Shooraj, Mahdi [11 ]
机构
[1] Univ Tehran Med Sci, Iranian Board Neurol, Tehran, Iran
[2] Kurdistan Board Neurol, Erbil, Iraq
[3] Zurich Univ, Fellowship Intervent Neuroradiol, Zurich, Switzerland
[4] Sabzevar Univ Med Sci, Noncommunicable Dis Res Ctr, Sabzevar, Iran
[5] Sabzevar Univ Med Sci, Student Res Comm, Sabzevar, Iran
[6] Shahid Beheshti Univ Med Sci, Sch Med, Dept Biol & Anat Sci, Tehran, Iran
[7] Tabriz Univ Med Sci, Fac Rehabil Sci, Dept Physiotherapy, Tabriz, Iran
[8] Mazandaran Univ Med Sci, Dept Immunol, Sch Med, Sari, Iran
[9] Mazandaran Univ Med Sci, Amol Sch Paramed Sci, Dept Paramed, Sari, Iran
[10] Islamic Azad Univ, Sch Pharmacol, Ayatollah Amoli Branch, Amol, Iran
[11] Mazandaran Univ Med Sci, Student Res Comm, Sari, Iran
关键词
Tramadol; Coenzyme Q10; Cerebellum; Apoptosis; Oxidative Stress; Inflammation; APOPTOSIS; AUTOPHAGY; TOXICITY; TISSUES; INJURY; INNATE; USAGE;
D O I
10.1016/j.jchemneu.2023.102367
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Chronic use of tramadol can cause neurotoxic effects and subsequently cause neurodegeneration in the cerebellum. The main damage mechanisms identified are oxidative stress and inflammation. Currently, we investigated the effects of coenzyme Q10 (CoQ10) in attenuates of neurodegeneration in the cerebellum induced by chronic exposure to tramadol.Material and methods: Seventy-two male mature albino rats were allocated into four equal groups, including; non-treated group, CoQ10 group (which received CoQ10 at 200 mg/kg/day orally for three weeks), tramadol group (which received tramadol hydrochloride at 50 mg/kg/day orally for three weeks), and tramadol+CoQ10 group (which received tramadol and CoQ10 at the same doses as the previous groups). Tissue samples were obtained for stereological, immunohistochemical, biochemical, and molecular evaluations. Also, functional tests were performed to evaluate behavioral properties.Results: We found a significant increase in stereological parameters, antioxidant factors (catalase, glutathione, and superoxide dismutase), and behavioral function scores in the tramadol+CoQ10 group compared to the tramadol group (p < 0.05). In addition, malondialdehyde levels, the density of apoptotic cells, as well as the expression of pro-inflammatory (tumor necrosis factor-alpha, interleukin 1 beta, and interleukin 6) and autophagy (lysosome-associated membrane protein 2, autophagy-related 5, beclin 1, and autophagy-related 12) genes were considerably reduced in the tramadol+CoQ10 group compared to the tramadol group (p < 0.05).Conclusion: We conclude that the administration of CoQ10 has neuroprotective effects in the cerebellum of rats that have chronic exposure to tramadol.
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页数:10
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