Maitra S R, Carretero O A, Smith S W, Rabito S F
Am J Physiol. 1986 Mar;250(3 Pt 1):C480-5. doi: 10.1152/ajpcell.1986.250.3.C480.
We investigated the role of calcium and calmodulin as intracellular mediators of kallikrein and tonin release induced by norepinephrine (NE). We studied the secretion rate of kallikrein and tonin from submandibular gland of rat in response to NE in the presence or absence of calcium, two calcium blockers, and four different calmodulin antagonists. Submandibular gland slices were incubated in vitro, and glandular kallikrein and tonin secreted into the incubation medium were determined by direct radioimmunoassays and expressed as nanograms per minute per milligram tissue. NE (10(-5) and 10(-4) M) increased the kallikrein secretion from the control value of 8.2 +/- 2.6 to 134.9 +/- 41.4 (P less than 0.05) and to 191.2 +/- 62.7 (P less than 0.05), and the release of tonin from a basal rate of 3.5 +/- 0.6 to 51.5 +/- 9.1 (P less than 0.05) and to 64.4 +/- 13.7 (P less than 0.05). The deletion of calcium and addition of EGTA into the incubation medium significantly attenuated the secretion of kallikrein and tonin induced by NE. Nifedipine, at concentrations which inhibit voltage-dependent calcium channels, did not affect the release of kallikrein and tonin, and only a high concentration (10(-4) M) reduced the release. TMB-8, a blocker of intracellular calcium, had no effect either. Phenothiazines, triflupromazine (10(-6) M) and trifluoperazine (10(-4) M), decreased significantly the kallikrein release elicited by 10(-5) M NE.(ABSTRACT TRUNCATED AT 250 WORDS)
我们研究了钙和钙调蛋白作为去甲肾上腺素(NE)诱导的激肽释放酶和血管紧张素原释放的细胞内介质的作用。我们研究了在有或无钙、两种钙阻滞剂和四种不同钙调蛋白拮抗剂存在的情况下,大鼠下颌下腺对NE的激肽释放酶和血管紧张素原分泌率。将下颌下腺切片进行体外孵育,通过直接放射免疫测定法测定分泌到孵育培养基中的腺激肽释放酶和血管紧张素原,并以每毫克组织每分钟纳克数表示。NE(10⁻⁵和10⁻⁴M)使激肽释放酶分泌从对照值8.2±2.6增加到134.9±41.4(P<0.05)和191.2±62.7(P<0.05),血管紧张素原释放从基础速率3.5±0.6增加到51.5±9.1(P<0.05)和64.4±13.7(P<0.05)。从孵育培养基中去除钙并添加乙二醇双四乙酸(EGTA)显著减弱了NE诱导的激肽释放酶和血管紧张素原分泌。硝苯地平在抑制电压依赖性钙通道的浓度下不影响激肽释放酶和血管紧张素原的释放,只有高浓度(10⁻⁴M)降低了释放。细胞内钙阻滞剂8-(N,N,N-三甲基铵)辛酸盐(TMB-8)也没有作用。吩噻嗪类药物,三氟丙嗪(10⁻⁶M)和三氟拉嗪(10⁻⁴M),显著降低了10⁻⁵M NE引起的激肽释放酶释放。(摘要截短于250字)