Garcia M M, Harlan R E
Department of Otolaryngology, University School of Medicine, New Orleans, LA 70112-2699.
Neuroreport. 1993 Oct 25;5(1):65-8. doi: 10.1097/00001756-199310000-00016.
The neuronal intracellular calcium-binding protein calbindin D28k is a neurochemical marker in the striatum, normally expressed in the matrix compartment and absent from the mu-opiate receptor-enriched striosomal (patch) compartment. Because chronic treatment with morphine has been reported to increase calcium levels in synaptosomes of rat striatum, we studied effects of morphine on calbindin immunoreactivity (ir) in rat brain, using immunocytochemistry. Treatment with morphine for 5 days increased calbindin-ir in the striatal matrix, and induced intense calbindin-ir in the patch compartment. Increased calbindin-ir in patches persisted through day 14 post-morphine. Co-administration of the NMDA receptor antagonist MK-801 blocked the morphine-induced increase in calbindin-ir in patches. We suggest that chronic morphine treatment may increase calcium and calbindin levels via increased glutamatergic transmission in striatum. These findings are consistent with reports that MK-801 inhibits tolerance to morphine, and provide a possible mechanism and anatomical substrate for this inhibition.
神经元细胞内钙结合蛋白钙结合蛋白D28k是纹状体中的一种神经化学标志物,通常在基质区室表达,而富含μ-阿片受体的纹状体小体(斑块)区室中不存在。由于据报道,长期用吗啡治疗会增加大鼠纹状体突触体中的钙水平,我们使用免疫细胞化学方法研究了吗啡对大鼠脑内钙结合蛋白免疫反应性(ir)的影响。用吗啡治疗5天可增加纹状体基质中的钙结合蛋白ir,并在斑块区室诱导强烈的钙结合蛋白ir。吗啡注射后第14天,斑块中增加的钙结合蛋白ir持续存在。同时给予NMDA受体拮抗剂MK-801可阻断吗啡诱导的斑块中钙结合蛋白ir的增加。我们认为,长期吗啡治疗可能通过增加纹状体中的谷氨酸能传递来增加钙和钙结合蛋白水平。这些发现与MK-801抑制对吗啡耐受性的报道一致,并为这种抑制提供了一种可能的机制和解剖学基础。