Department of Biomedical Sciences, Pharmacology Division, College of Medicine, King Faisal University, Al-Ahsa, Saudi Arabia.
Life Sci. 2012 Sep 17;91(7-8):284-92. doi: 10.1016/j.lfs.2012.07.030. Epub 2012 Aug 1.
To investigate the protective effect of cannabidiol, the major non-psychotropic Cannabis constituent, against renal ischemia/reperfusion injury in rats.
Bilateral renal ischemia was induced for 30 min followed by reperfusion for 24h. Cannabidiol (5mg/kg, i.v.) was given 1h before and 12h following the procedure.
Ischemia/reperfusion caused significant elevations of serum creatinine and renal malondialdehyde and nitric oxide levels, associated with a significant decrease in renal reduced glutathione. Cannabidiol significantly attenuated the deterioration in the measured biochemical parameters induced by ischemia/reperfusion. Histopathological examination showed that cannabidiol ameliorated ischemia/reperfusion-induced kidney damage. Immunohistochemical analysis revealed that cannabidiol significantly reduced the expression of inducible nitric oxide synthase, tumor necrosis factor-α, cyclooxygenase-2, nuclear factor-κB, Fas ligand and caspase-3, and increased the expression of survivin in ischemic/reperfused kidney tissue.
Cannabidiol, via its antioxidant and anti-inflammatory properties, may represent a potential therapeutic option to protect against ischemia/reperfusion renal injury.
研究大麻的主要非精神活性成分大麻二酚(CBD)对大鼠肾缺血/再灌注损伤的保护作用。
双侧肾脏缺血 30 分钟,然后再灌注 24 小时。在该过程前 1 小时和后 12 小时给予 CBD(5mg/kg,静脉注射)。
缺血/再灌注导致血清肌酐和肾丙二醛及一氧化氮水平显著升高,同时肾还原型谷胱甘肽水平显著降低。CBD 显著减轻了缺血/再灌注引起的生化参数的恶化。组织病理学检查显示,CBD 改善了缺血/再灌注引起的肾脏损伤。免疫组化分析显示,CBD 显著降低了诱导型一氧化氮合酶、肿瘤坏死因子-α、环氧化酶-2、核因子-κB、Fas 配体和半胱天冬酶-3的表达,同时增加了缺血/再灌注肾组织中存活素的表达。
CBD 通过其抗氧化和抗炎特性,可能成为一种潜在的治疗选择,以防止缺血/再灌注肾损伤。