Rahmani N H, Gulati A, Bhargava H N
Department of Pharmacodynamics (m/c 865), University of Illinois, Chicago, IL 60612.
Peptides. 1990 Jul-Aug;11(4):693-5. doi: 10.1016/0196-9781(90)90182-5.
The effect of chronic administration of morphine and its withdrawal on the binding of 3H-[3-MeHis2]thyrotropin releasing hormone (3H-MeTRH) to membranes of the spinal cord of the rat was determined. Male Sprague-Dawley rats were implanted with either 6 placebo or 6 morphine pellets (each containing 75-mg morphine base) during a 7-day period. Two sets of animals were used. In one, the pellets were left intact at the time of sacrificing (tolerant-dependent) and in the other, the pellets were removed 16 hours prior to sacrificing (abstinent rats). In placebo-pellet-implanted rats, 3H-MeTRH bound to the spinal cord membranes at a single high affinity binding site with a Bmax of 21.3 +/- 1.6 fmol/mg protein, and an apparent dissociation constant Kd of 4.7 +/- 0.8 nM. In morphine tolerant-dependent or abstinent rats, the binding constants of 3H-MeTRH to spinal cord membranes were unaffected. Previous studies from this laboratory indicate that TRH can inhibit morphine tolerance-dependence and abstinence processes without modifying brain TRH receptors. Together with the present results, it appears that the inhibitory effect of TRH on morphine tolerance-dependence and abstinence is probably not mediated via central TRH receptors but may be due to its interaction with other neurotransmitter systems.
测定了长期给予吗啡及其撤药对3H-[3-甲基组氨酸2]促甲状腺激素释放激素(3H-MeTRH)与大鼠脊髓膜结合的影响。雄性Sprague-Dawley大鼠在7天内植入6个安慰剂或6个吗啡丸(每个含75毫克吗啡碱)。使用了两组动物。一组在处死时丸剂保持完整(耐受依赖组),另一组在处死前16小时取出丸剂(戒断大鼠)。在植入安慰剂丸的大鼠中,3H-MeTRH在单个高亲和力结合位点与脊髓膜结合,Bmax为21.3±1.6 fmol/mg蛋白,表观解离常数Kd为4.7±0.8 nM。在吗啡耐受依赖或戒断大鼠中,3H-MeTRH与脊髓膜的结合常数未受影响。该实验室以前的研究表明,TRH可抑制吗啡耐受依赖和戒断过程,而不改变脑TRH受体。结合目前的结果,似乎TRH对吗啡耐受依赖和戒断的抑制作用可能不是通过中枢TRH受体介导的,而是可能由于其与其他神经递质系统的相互作用。