Jakubovic A, McGeer E G, McGeer P L
Mol Cell Endocrinol. 1979 Jul;15(1):41-50. doi: 10.1016/0303-7207(79)90069-8.
Various water-insoluble cannabinoids as well as SP-111A, the water-soluble derivative of delta 9-tetrahydrocannabinol (delta 9-THC), reduced hCG and dibutyryl-cAMP stimulated testosterone production by rat testicular Leydig cell preparations. With 0.15 microM (0.05 micrograms/ml) 8-beta-OH-delta 9-THC the inhibition was about 50% of stimulated testosterone synthesis. Dose-related inhibitions were apparent with other cannabinoids and their order of potency in inhibiting stimulated steroidogenesis by the interstitial cells in vitro was found to be: 8-beta-OH-delta 9-THC greater than or equal to 11-OH-delta 9-THC greater than CBN = CBD = CBG greater than or equal delta 9-THC = delta 8-THC. The non-stimulated, basal, steroidogenesis was not affected even with 15 microM cannabinoids. The incorporation of L-[U-14C]leucine into the protein of Leydig cells was markedly reduced by 15 microM cannabinoids under both basal and stimulated conditions. The inhibition of steroidogenesis as well as protein synthesis in rat testicular Leydig cell preparations by various cannabinoids cannot be correlated with their psychoactivity. The present data suggest that cannabinoids at very low concentrations may interfere directly in Leydig cells with both protein and testosterone synthesis, and thus with their function.
多种水不溶性大麻素以及SP - 111A(δ9 - 四氢大麻酚(δ9 - THC)的水溶性衍生物),可降低大鼠睾丸间质细胞制剂中由人绒毛膜促性腺激素(hCG)和二丁酰环磷腺苷(dibutyryl - cAMP)刺激产生的睾酮。使用0.15微摩尔/升(0.05微克/毫升)的8 - β - 羟基 - δ9 - THC时,抑制作用约为刺激睾酮合成量的50%。其他大麻素也呈现出剂量相关的抑制作用,并且发现它们在体外抑制间质细胞刺激类固醇生成的效力顺序为:8 - β - 羟基 - δ9 - THC≥11 - 羟基 - δ9 - THC>大麻酚(CBN) = 大麻二酚(CBD) = 大麻萜酚(CBG)≥δ9 - THC = δ8 - THC。即使使用15微摩尔/升的大麻素,非刺激状态下的基础类固醇生成也未受影响。在基础和刺激条件下,15微摩尔/升的大麻素均显著降低了L - [U - 14C]亮氨酸掺入间质细胞蛋白质中的量。各种大麻素对大鼠睾丸间质细胞制剂中类固醇生成以及蛋白质合成的抑制作用与其精神活性无关。目前的数据表明,极低浓度的大麻素可能直接干扰间质细胞中的蛋白质和睾酮合成,进而影响其功能。