Yano K, Sorimachi M
Department of Surgery and Physiology, Kagoshima University, School of Medicine, Japan.
Jpn J Physiol. 1989;39(2):283-301. doi: 10.2170/jjphysiol.39.283.
Catecholamine (CA) secretion induced by Ca re-introduction or ouabain in the presence of Ca is markedly potentiated by Bay-K-8644 in the perfused cat adrenal. The mechanism of potentiation by this Ca agonist was investigated using perfused cat adrenal and isolated bovine chromaffin cells. The stimulatory effect of Bay-K-8644 on the response to Ca was very slight when cat adrenal was perfused with a Ca-deficient medium, in which 1 mM Mg was added or the concentration of Na was lowered. The inhibitory effect of Mg was reversed by inhibition of the Na pump with K deprivation, ouabain, or KCN. The secretion induced by ouabain during maintained depolarization at a lowered concentration (0.25 mM) of Ca, which is supposed to be due to Ca influx in exchange for Na efflux, was larger in the Bay-K-8644 treated adrenal than that in the untreated adrenal. The increase in secretion by the delayed addition of Bay-K-8644 during perfusion with a high K medium containing ouabain was larger when the concentration of Na in a high K medium was higher. When isolated chromaffin cells were stimulated with a Na-free (Tris) medium containing 0.5 mM Ca, CA secretion from and 45Ca uptake into the cells preincubated with a divalent cation-free medium were potentiated by Bay-K-8644. The stimulatory effect of Bay-K-8644 was not seen when a Ca-free treatment medium contained Mg or lacked Na, but the inhibitory effect of Mg was reversed by the addition of ouabain or KCN to the pretreatment medium. When isolated cells preloaded with 45Ca were superfused with a Ca-free medium, Ca re-introduction increased the rate of Ca efflux only under conditions in which significant increases in CA secretion and 45Ca uptake were previously observed under the static incubation system. Bay-K-8644 further increased this Ca efflux rate under these conditions. These results support the view that Ca influx linked with Na efflux is through a pathway with properties similar to those of voltage-dependent Ca channels, and suggest that this Ca pathway is activated by Bay-K-8644, which is an activator of voltage-dependent Ca channels.
在灌注的猫肾上腺中,Bay-K-8644可显著增强在重新引入钙或存在钙的情况下哇巴因诱导的儿茶酚胺(CA)分泌。使用灌注的猫肾上腺和分离的牛嗜铬细胞研究了这种钙激动剂的增强机制。当用添加了1 mM镁或降低了钠浓度的缺钙培养基灌注猫肾上腺时,Bay-K-8644对钙反应的刺激作用非常轻微。通过剥夺钾、哇巴因或氰化钾抑制钠泵可逆转镁的抑制作用。在较低浓度(0.25 mM)的钙维持去极化过程中,哇巴因诱导的分泌(推测是由于钙内流以交换钠外流)在经Bay-K-864治疗的肾上腺中比未治疗的肾上腺中更大。当在含有哇巴因的高钾培养基灌注期间延迟添加Bay-K-8644时,高钾培养基中钠浓度越高,分泌增加越大。当用含有0.5 mM钙的无钠(Tris)培养基刺激分离的嗜铬细胞时,预先用无二价阳离子培养基孵育的细胞的CA分泌和45Ca摄取可被Bay-K-8644增强。当无钙处理培养基含有镁或缺乏钠时,未观察到Bay-K-8644的刺激作用,但通过向预处理培养基中添加哇巴因或氰化钾可逆转镁的抑制作用。当用无钙培养基对预先加载45Ca的分离细胞进行灌流时,只有在静态孵育系统中先前观察到CA分泌和45Ca摄取显著增加的条件下,重新引入钙才会增加钙外流速率。在这些条件下,Bay-K-8644进一步提高了这种钙外流速率。这些结果支持了与钠外流相关的钙内流是通过一条与电压依赖性钙通道特性相似的途径的观点,并表明这条钙途径被Bay-K-8644激活,Bay-K-8644是一种电压依赖性钙通道激活剂。