4.7 Article

Reversal effect of simvastatin on the decrease in cannabinoid receptor 1 density in 6-hydroxydopamine lesioned rat brains

Journal

LIFE SCIENCES
Volume 155, Issue -, Pages 123-132

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.lfs.2016.05.005

Keywords

Parkinson's disease; Cannabinoid 1 receptor; 6-hydroxydopamine; Simvastatin; [H-3] SR141716A

Funding

  1. National Natural Science Foundations of China [81271427, 81471291]
  2. 973 Project [2011CB510000]
  3. Scientific Research Foundation of Guangzhou [2014J4100210]
  4. Science and Technology Program of Guangdong of China [2016A050502019]
  5. Guangdong Department of Science & Technology Translational Medicine Center Grant [2011A080300002]
  6. Australia National Health and Medical Research Council Grant (NHMRC) [ID: 514640]
  7. Schizophrenia Research Institute

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Aims: Cannabinoid 1(CB1) receptors are closely correlated to the dopaminergic system and involved in cognitive function. Since wstatins have been used to regulate the progression of Parkinson's disease (PD) via its anti-inflammation and neuroprotective effects, we asked if statins affect the CB1 receptors in the 6-hydroxydopamine (6-OHDA) lesioned rat. Methods: The PD rat model was established by injecting 6-OHDA into the unilateral medial forebrain bundle; while rats were orally pre-treated with simvastatin (1 or 10 mg/kg/day), or saline for 5 days before surgery, and the same treatments for each group were continued for 3 weeks post-surgery. [H-3] SR141716A binding autoradiography was adopted to investigate the alterations in CB1 receptor density in the brains. Findings: The 6-OHDA induced a remarkable downregulation of CB1 receptor density in the prefrontal cortex, caudate putamen, nucleus accumbens, cingulate cortex, hippocampus, and substantia nigra; while simvastatin (10 mg/kg/day) significantly ameliorated this downregulation in those regions. Furthermore, simvastatin (1 mg/kg/day) reversed the 6-OHDA-induced downregulation of CB1 receptors in the substantia nigra and hippocampus. Simvastatin showed minimal changes in [H-3] SR141716A binding in the examined regions in sham rats, but did reveal a significant down-regulation of binding density within the striatum, prefrontal cortex and substantia nigra. Significance: Alterations in the [H-3] SR141716A binding in the examined brain areas may represent the specific regions that mediate motor and cognitive dysfunctions in PD via the endocannabinoid system. Our data suggest a critical role of CB1 receptors in treating PD with simvastatin, and implicate CB1 receptors as a potential therapeutic target in the treatment of PD. (C) 2016 Elsevier Inc. All rights reserved.

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