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鲑鱼降钙素诱导的细胞内游离钙调节

Salmon calcitonin-induced modulation of free intracellular calcium.

作者信息

Welch S P, Olson K G

机构信息

Department of Pharmacology and Toxicology, Virginia Commonwealth University/Medical College of Virginia, Richmond 23298.

出版信息

Pharmacol Biochem Behav. 1991 Jul;39(3):641-8. doi: 10.1016/0091-3057(91)90140-w.

Abstract

Salmon calcitonin (sCT), a hormone shown to modulate calcium in the periphery modulated free, intracellular calcium, ([Ca++]i), in mouse brain synaptosomes as measured by changes in fura-2-mediated fluorescence. A 5-min incubation of synaptosomes with sCT produced an increase in the basal levels of [Ca++]i and an increase in KCl-stimulated levels of [Ca++]i. A 5-min pretreatment of mice with intraventricularly administered sCT antagonized morphine-induced antinociception in the tail-flick test, and facilitated naloxone antagonism of morphine. Conversely, pretreatment of synaptosomes for 1 h with salmon CT produced a decrease in depolarization-stimulated levels of [Ca++]i. The sCT-induced decrease in the stimulated rise in [Ca++]i at 1 h correlated temporally to sCT-induced antinociception in vivo. The effects of sCT in the electrically stimulated guinea pig ileum bioassay appeared to correlate to sCT effects in vivo. The data indicate that calcitonin may function as a neuromodulator via modulation of Ca++ within the central nervous system.

摘要

鲑鱼降钙素(sCT)是一种在外周可调节钙的激素,它能调节小鼠脑突触体中游离的细胞内钙([Ca++]i),这是通过fura-2介导的荧光变化来测量的。突触体与sCT孵育5分钟会使[Ca++]i的基础水平升高,同时KCl刺激的[Ca++]i水平也升高。给小鼠脑室内注射sCT进行5分钟预处理,在甩尾试验中可拮抗吗啡诱导的镇痛作用,并促进纳洛酮对吗啡的拮抗作用。相反,用鲑鱼降钙素对突触体进行1小时预处理会使去极化刺激的[Ca++]i水平降低。1小时时sCT诱导的[Ca++]i刺激升高的降低与sCT在体内诱导的镇痛作用在时间上相关。sCT在电刺激豚鼠回肠生物测定中的作用似乎与sCT在体内的作用相关。数据表明,降钙素可能通过调节中枢神经系统内的Ca++发挥神经调节剂的作用。

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