Horta J, Cota G
Department of Physiology, Biophysics, and Neurosciences, Centro de Investigacion y de Estudios Avanzados, Mexico City, DF.
Mol Cell Endocrinol. 1993 Apr;92(2):189-93. doi: 10.1016/0303-7207(93)90007-7.
Pituitary cultures from adult rats contain two subtypes of prolactin (PRL) cells, small-plaque (SP) and large-plaque (LP) lactotropes, which exhibit distinct rates of basal secretion and thereby form PRL plaques of different sizes in reverse hemolytic plaque assay experiments. In the present study, we have used plaque assays to examine the effects of omega-conotoxin (omega-CgTx) and nifedipine, which block Ca2+ entry through high voltage-activated (HVA) channels in the plasma membrane, on basal PRL secretion from single male rat lactotropes. We found that omega-CgTx, like nifedipine, is a potent inhibitor of PRL secretion. In addition, we observed that both drugs decrease the number of cells forming large PRL plaques, while promoting a comparable increase in the abundance of small plaque formers. The results indicate that blocking the HVA Ca channels preferentially suppresses PRL release from LP lactotropes, and suggest that the inhibited PRL secretors tend to behave functionally as SP lactotropes.
成年大鼠的垂体培养物中含有两种催乳素(PRL)细胞亚型,即小斑块(SP)和大斑块(LP)促乳素细胞,它们在基础分泌速率上表现出明显差异,因此在反向溶血空斑试验中形成不同大小的PRL斑块。在本研究中,我们使用空斑试验来检测ω-芋螺毒素(ω-CgTx)和硝苯地平对雄性大鼠单个促乳素细胞基础PRL分泌的影响,这两种物质可阻断质膜中高电压激活(HVA)通道的Ca2+内流。我们发现,ω-CgTx与硝苯地平一样,是PRL分泌的有效抑制剂。此外,我们观察到这两种药物都减少了形成大PRL斑块的细胞数量,同时促进了形成小斑块细胞数量的相应增加。结果表明,阻断HVA钙通道优先抑制LP促乳素细胞释放PRL,并表明受抑制的PRL分泌细胞在功能上倾向于表现为SP促乳素细胞。