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药物诱导的鱼类视网膜儿茶酚胺能细胞变化。

Drug-induced changes in catecholaminergic cells of the fish retina.

作者信息

Negishi K, Laufer M, Drujan B D

出版信息

J Neurosci Res. 1980;5(6):599-609. doi: 10.1002/jnr.490050614.

Abstract

The changes in fluorescence intensity and number of visible catecholaminergic cells (CA-cells), as revealed by means of a histofluorescence technique, were used as indicators of the effects of various pharmacological agents upon CA-cells in the retina of fishes (Cyprinus carpio and Eugerres plumieri). The study includes in vivo and in vitro experiments. In the in vivo experiments, intravitreal injection, two or three hours before eye enucleation, of 10 microgram L-DOPA, dopamine, or noradrenaline accentuated CA-cell fluorescence and increased the number of visible cells, whereas 10 microgram of tyramine, octopamine, synephrine, or adrenaline reduced the endogenous fluorescence. Intramuscular injection of reserpine (3 mg/kg) abolished CA-cell fluorescence. In the in vitro experiments, pieces of isolated retinas were incubated for three or 30 minutes in media containing different drugs. Only minor changes in fluorescence were detected after three minutes of incubation, but after 30 minutes, dopamine (20 microM) markedly enhanced CA-cell fluorescence. Carbachol (20 mM), acetylcholine (10 mM) plus BW-anticholinesterase (1 mM) or substance P(1.6 x 10(-2) mM), all reduced CA-cell fluorescence. Kainic acid (20 mM) abolished fluorescence from CA-cell somata, while fluorescent fiber networks remain unchanged. L-aspartate (5 mM) and GABA (10 mM) in the incubation medium did not influence fluorescence intensity. The results are relevant to, and consistent with, electrophysiological observations of dopamine-mediated spatial effects on horizontal cell potentials.

摘要

通过组织荧光技术揭示的荧光强度变化以及可见儿茶酚胺能细胞(CA细胞)数量的变化,被用作各种药理剂对鱼类(鲤鱼和银汉鱼)视网膜中CA细胞作用的指标。该研究包括体内和体外实验。在体内实验中,在摘除眼球前两到三小时玻璃体内注射10微克左旋多巴、多巴胺或去甲肾上腺素,可增强CA细胞荧光并增加可见细胞数量,而10微克酪胺、章鱼胺、辛弗林或肾上腺素则可降低内源性荧光。肌肉注射利血平(3毫克/千克)可消除CA细胞荧光。在体外实验中,将分离的视网膜片在含有不同药物的培养基中孵育三或30分钟。孵育三分钟后仅检测到荧光有微小变化,但孵育30分钟后,多巴胺(20微摩尔)显著增强了CA细胞荧光。卡巴胆碱(20毫摩尔)、乙酰胆碱(10毫摩尔)加BW抗胆碱酯酶(1毫摩尔)或P物质(1.6×10⁻²毫摩尔)均降低了CA细胞荧光。 kainic酸(20毫摩尔)消除了CA细胞胞体的荧光,而荧光纤维网络保持不变。孵育培养基中的L - 天冬氨酸(5毫摩尔)和GABA(10毫摩尔)不影响荧光强度。这些结果与多巴胺介导的对水平细胞电位的空间效应的电生理观察结果相关且一致。

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