Bartova A, Birmingham M K
J Biol Chem. 1976 Aug 25;251(16):5002-6.
Delta9-Tetrahydrocannabinol (delta9-THC), the active ingredient of marihuana was found to be a highly effective inhibitor in vitro of the NADH-oxidase activity of rat brain and heart mitochondria. The degree of inhibition of the enzyme system obtained from rat brain tissue varied with the region from which it was derived as follows, in the presence of 10(-5) M delta9-THC: hypothalamus plus thalamus plus midbrain, 73 +/- 4%; cerebellum, 66 +/- 4%; medulla oblongata plus pons, 63 +/- 6%; cerebral cortex, 50 +/- 8%. The same concentration inhibited rat heart NADH-oxidase activity 69 +/- 9%. Inhibition of NADH-oxidase activity by a corresponding concentration of deoxycorticosterone was significantly less in all tissue preparations tested, ranging from 11% to 26%. The inhibition of delta9-THC appeared to be competitive and near the amytal-sensitive site of the electron transport system. Suggestive evidence was also obtained for a second site of action, above the cytochrome c site.
Δ⁹-四氢大麻酚(Δ⁹-THC),即大麻的活性成分,被发现是大鼠脑和心肌线粒体NADH氧化酶活性的一种高效体外抑制剂。从大鼠脑组织获得的酶系统的抑制程度随其来源区域而变化,如下所示,在存在10⁻⁵M Δ⁹-THC的情况下:下丘脑加丘脑加中脑,73±4%;小脑,66±4%;延髓加脑桥,63±6%;大脑皮层,50±8%。相同浓度抑制大鼠心脏NADH氧化酶活性69±9%。在所有测试的组织制剂中,相应浓度的脱氧皮质酮对NADH氧化酶活性的抑制明显较小,范围为11%至26%。Δ⁹-THC的抑制作用似乎具有竞争性,且接近电子传递系统的巴比妥类敏感位点。还获得了提示性证据,表明存在第二个作用位点,位于细胞色素c位点之上。