Repository of Research and Investigative Information

Repository of Research and Investigative Information

Dezful University of Medical Sciences

Venlafaxine prevents morphine antinociceptive tolerance: The role of neuroinflammation and the L-arginine-nitric oxide pathway

(2018) Venlafaxine prevents morphine antinociceptive tolerance: The role of neuroinflammation and the L-arginine-nitric oxide pathway. Experimental Neurology. pp. 134-141. ISSN 0014-4886

Full text not available from this repository.

Official URL: http://apps.webofknowledge.com/InboundService.do?F...

Abstract

Opioid-induced neuroinflammation and the nitric oxide (NO) signal-transduction pathway are involved in the development of opioid analgesic tolerance. The antidepressant venlafaxine (VLF) modulates NO in nervous tissues, and so we investigated its effect on induced tolerance to morphine, neuroinflammation, and oxidative stress in mice. Tolerance to the analgesic effects of morphine were induced by injecting mice with morphine (50 mg/kg) once a day for three consecutive days; the effect of co-administration of VLF (5 or 40 mg/kg) with morphine was similarly tested in a separate group. To determine if the NO precursor L-arginine hydrochloride (L-arg) or NO are involved in the effects rendered by VLF, animals were pre-treated with L-arg (200 mg/kg), or the NO synthesis inhibitors N(omega)-nitro-L-arginine methyl ester (L-NAME; 30 mg/kg) or aminoguanidine hydrochloride (AG; 100 mg/kg), along with VLF (40 mg/kg) for three days before receiving morphine for another three days. Nociception was assessed with a hot-plate test on the fourth day, and the concentration of tumor necrosis factor alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), interleukin-10, brain-derived neurotrophic factor, NO, and oxidative stress factors such as total thiol, malondialdehyde content, and glutathione peroxidase (GPx) activity in the brain was also determined. Co-administration of VLF with morphine attenuated morphine-induced analgesic tolerance and prevented the upregulation of proinflammatory cytokines (TNF-alpha, IL-1 beta, and IL-6), NO, and malondialdehyde in brains of mice with induced morphine tolerance; chronic VLF administration inhibited this decrease in brain-derived neurotrophic factor, total thiol, and GPx levels. Moreover, repeated administration of L-arg before receipt of VLF antagonized the effects induced by VLF, while L-NAME and AG potentiated these effects. VLF attenuates morphine-induced analgesic tolerance, at least partly because of its anti-inflammatory and antioxidative properties. VLF also appears to suppress the development of morphine-induced analgesic tolerance through an L-arg-NO-mediated mechanism.

Item Type: Article
Keywords: Morphine tolerance Venlafaxine Cytokines L-arg-NO pathway Neuroinflammation Oxidative stress Brain-derived neurotrophic factor neurotrophic factor ellagic acid neuropathic pain oxidative stress frontal-cortex spinal-cord tnf-alpha brain expression dependence Neurosciences & Neurology
Subjects: QU Biochemistry. Cell Biology and Genetics > QU 100-133 Biochemistry of the Human Body
Divisions: Education Vice-Chancellor Department > Faculty of Pharmacy > Department of Toxicology and Pharmacology
Page Range: pp. 134-141
Journal or Publication Title: Experimental Neurology
Journal Index: ISI
Volume: 303
Identification Number: https://doi.org/10.1016/j.expneurol.2018.02.009
ISSN: 0014-4886
Depositing User: مهندس مهدی شریفی
URI: http://eprints.dums.ac.ir/id/eprint/137

Actions (login required)

View Item View Item