Bonnin A, Fernández-Ruiz J J, Martín M, Rodríguez de Fonseca F, Hernández M L, Ramos J A
Department of Biochemistry, Faculty of Medicine, Complutense University, Madrid, Spain.
J Neural Transm Gen Sect. 1993;92(2-3):81-95. doi: 10.1007/BF01244868.
In this work, we studied the possible estrogenic modulation of the effects of delta 9-tetrahydrocannabinol (THC) on mesolimbic dopaminergic activity, by examining the effects of an acute dose of this cannabinoid: (i) during the estrous cycle; (ii) after ovariectomy, chronic estrogen-replacement and tamoxifen (TMX)-induced blockade of estrogenic receptors; and (iii) combined with a single and physiological injection of estradiol to ovariectomized rats. THC significantly decreased the density of D 1 dopaminergic receptors and non-significantly increased the L-3,4-dihydroxyphenylacetic acid (DOPAC) content in the limbic forebrain of ovariectomized rats chronically replaced with estrogens. The decrease in D 1 receptors was also produced by TMX, whereas the coadministration of both THC and TMX did not lead to a major decrease. In addition to the trend of THC increasing DOPAC content, this cannabinoid was also able to increase the ratio between DOPAC and dopamine, although this last effect only occurred after coadministration of THC and TMX, which had been ineffective administered individually. All these effects were not seen when THC was administered to normal cycling rats during each phase of estrous cycle and to ovariectomized rats without chronic estrogen replacement or only submitted to a single and acute dose of estradiol. This observation might be related to the fact that the density of limbic cannabinoid receptors increased in chronic estrogen-replaced ovariectomized rats versus normal cycling, ovariectomized or acutely estrogen-treated ovariectomized rats. Interestingly, THC administration in ovariectomized rats was followed by a slight, although significant, increase in tyrosine hydroxylase activity, which was also observed after coadministration of THC with a short-time and acute dose of estradiol. In summary, THC stimulated the presynaptic activity of mesolimbic dopaminergic neurons, but accompanied by a decrease in their postsynaptic sensitivity. These effects did not appear in normal cycling rats being only evident after ovariectomy and chronic estrogen replacement, which might be related to changes in binding characteristics of cannabinoid receptors in this area. Moreover, some of them appeared after TMX-induced blockade of estrogenic cytosolic receptors, which likely suggests the existence of a certain estrogenic modulation of the actions of THC on mesolimbic neurons. On the contrary, coadministration of THC with a single and shortly tested dose of estradiol was always ineffective in modifying THC effects.
在本研究中,我们通过检测急性剂量的δ9 - 四氢大麻酚(THC)的作用,研究其对中脑边缘多巴胺能活性的潜在雌激素调节作用:(i)在发情周期中;(ii)卵巢切除术后、长期雌激素替代及他莫昔芬(TMX)诱导的雌激素受体阻断后;(iii)与向去卵巢大鼠单次生理剂量注射雌二醇联合使用时。THC显著降低了长期接受雌激素替代的去卵巢大鼠边缘前脑D1多巴胺能受体的密度,并使L - 3,4 - 二羟基苯乙酸(DOPAC)含量有不显著增加。TMX也导致了D1受体的减少,而THC与TMX联合给药并未导致D1受体的进一步显著减少。除了THC使DOPAC含量增加的趋势外,该大麻素还能够增加DOPAC与多巴胺的比值,不过这一效应仅在THC与TMX联合给药后出现,单独给药时二者均无效。当在发情周期各阶段给正常循环大鼠以及未进行长期雌激素替代或仅接受单次急性剂量雌二醇的去卵巢大鼠给予THC时,未观察到上述所有效应。这一观察结果可能与以下事实有关:与正常循环、去卵巢或急性雌激素处理的去卵巢大鼠相比,长期雌激素替代的去卵巢大鼠边缘大麻素受体密度增加。有趣的是,给去卵巢大鼠注射THC后,酪氨酸羟化酶活性有轻微但显著的增加,在THC与短期急性剂量雌二醇联合给药后也观察到了这一现象。总之,THC刺激了中脑边缘多巴胺能神经元的突触前活性,但同时伴随着其突触后敏感性的降低。这些效应在正常循环大鼠中未出现,仅在卵巢切除术后和长期雌激素替代后明显,这可能与该区域大麻素受体结合特性的变化有关。此外,其中一些效应在TMX诱导的雌激素胞质受体阻断后出现,这可能表明存在对THC作用于中脑边缘神经元的某种雌激素调节。相反,THC与单次短期检测剂量雌二醇联合给药在改变THC效应方面始终无效。