Kalisch B E, Jhamandas K, Boegman R J, Beninger R J
Department of Pharmacology, Queen's University, Kingston, Ont., Canada.
Brain Res. 1994 Dec 30;668(1-2):1-8. doi: 10.1016/0006-8993(94)90504-5.
Previous studies in our laboratory have demonstrated that focal injections of picolinic acid (PIC) protect the cholinergic neurons of the nucleus basalis magnocellularis (nbm) against quinolinic acid (QUIN)-induced neurotoxicity. The present study was designed to examine the effects of chronic infusions of QUIN and PIC on nicotinamide adenine dinucleotide (NADPH) diaphorase containing neurons of the rat striatum. Using osmotic minipumps, QUIN (6 nmol/h) and PIC (18 nmol/h) were infused alone or in combination to examine the neurotoxic effects of QUIN and the potential anti-neurotoxic action of PIC. Exposure to QUIN for 7 days severely depleted NADPH diaphorase-positive neurons. When co-infused with this neurotoxic dose of QUIN, PIC attenuated the depletion of NADPH diaphorase neurons induced by QUIN. The infusion of PIC alone did not affect the number of these neurons. These results indicate that PIC itself is not neurotoxic and effectively prevents chronic QUIN-induced neurotoxicity in the rat striatum. Since PIC and QUIN are derived from the same metabolic pathway, a balance between endogenous compounds that produce neurotoxicity and those antagonizing these effects may be important in normal neuronal function.
我们实验室之前的研究表明,向局部注射吡啶甲酸(PIC)可保护大细胞基底核(nbm)的胆碱能神经元免受喹啉酸(QUIN)诱导的神经毒性。本研究旨在检测长期输注QUIN和PIC对大鼠纹状体中含烟酰胺腺嘌呤二核苷酸磷酸(NADPH)黄递酶的神经元的影响。使用渗透微型泵,单独或联合输注QUIN(6 nmol/h)和PIC(18 nmol/h),以检测QUIN的神经毒性作用以及PIC潜在的抗神经毒性作用。暴露于QUIN 7天会严重消耗NADPH黄递酶阳性神经元。当与该神经毒性剂量的QUIN联合输注时,PIC可减轻QUIN诱导的NADPH黄递酶神经元的消耗。单独输注PIC不会影响这些神经元的数量。这些结果表明,PIC本身无神经毒性,并且可有效预防大鼠纹状体中慢性QUIN诱导的神经毒性。由于PIC和QUIN源自相同的代谢途径,因此在正常神经元功能中,产生神经毒性的内源性化合物与拮抗这些作用的化合物之间的平衡可能很重要。