Departamento Neurociencia Cognitiva, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Ciudad Universitaria, 04510, Ciudad de México, México.
Cátedras CONACyT, Instituto Nacional de Psiquiatría Ramón de La Fuente Muñiz, Laboratorio de Fisiología Celular, Calzada México Xochimilco No. 101, Ciudad de México, 14370, México.
Pflugers Arch. 2021 Nov;473(11):1775-1793. doi: 10.1007/s00424-021-02614-2. Epub 2021 Sep 11.
The hypersecretory phenotype of adrenal chromaffin cells (CCs) from early spontaneously hypertensive rats (SHRs) mainly results from enhanced Ca-induced Ca-release (CICR). A key question is if these abnormalities can be traced to the prehypertensive stage. Spontaneous and stimulus-induced catecholamine exocytosis, intracellular Ca signals, and dense-core granule size and density were examined in CCs from prehypertensive and hypertensive SHRs and compared with age-matched Wistar-Kyoto rats (WKY). During the prehypertensive stage, the depolarization-elicited catecholamine exocytosis was ~ 2.9-fold greater in SHR than in WKY CCs. Interestingly, in half of CCs the exocytosis was indistinguishable from WKY CCs, while it was between 3- and sixfold larger in the other half. Likewise, caffeine-induced exocytosis was ~ twofold larger in prehypertensive SHR. Accordingly, depolarization and caffeine application elicited [Ca]i rises ~ 1.5-fold larger in prehypertensive SHR than in WKY CCs. Ryanodine reduced the depolarization-induced secretion in prehypertensive SHR by 57%, compared to 14% in WKY CCs, suggesting a greater contribution of intracellular Ca release to exocytosis. In SHR CCs, the mean spike amplitude and charge per spike were significantly larger than in WKY CCs, regardless of age and stimulus type. This difference in granule content could explain in part the enhanced exocytosis in SHR CCs. However, electron microscopy did not reveal significant differences in granule size between SHRs and WKY rats' adrenal medulla. Nonetheless, preSHR and hypSHR display 63% and 82% more granules than WKY, which could explain in part the enhanced catecholamine secretion. The mechanism responsible for the heterogeneous population of prehypertensive SHR CCs and the bias towards secreting more medium and large granules remains unexplained.
肾上腺嗜铬细胞(CCs)的高分泌表型主要是由于增强的 Ca2+诱导的 Ca2+释放(CICR)所致。一个关键问题是这些异常是否可以追溯到高血压前期。本研究在高血压前期和高血压自发性高血压大鼠(SHR)的 CCs 中检测了自发性和刺激诱导的儿茶酚胺胞吐、细胞内 Ca 信号、致密核心颗粒大小和密度,并与年龄匹配的 Wistar-Kyoto 大鼠(WKY)进行了比较。在高血压前期,SHR 的去极化诱发儿茶酚胺胞吐作用比 WKY CC 高约 2.9 倍。有趣的是,在一半的 CCs 中,胞吐作用与 WKY CC 无法区分,而在另一半中则高 3 至 6 倍。同样,咖啡因诱导的胞吐作用在高血压前期 SHR 中高约 2 倍。因此,与 WKY CC 相比,高血压前期 SHR 中去极化和咖啡因应用诱发的 [Ca]i 升高高约 1.5 倍。与 WKY CC 相比,瑞诺定使高血压前期 SHR 中去极化诱导的分泌减少了 57%,而 WKY CC 减少了 14%,表明细胞内 Ca2+释放对胞吐作用的贡献更大。在 SHR CCs 中,无论年龄和刺激类型如何,尖峰幅度和每尖峰电荷量的平均值均明显大于 WKY CCs。这种颗粒含量的差异可以部分解释 SHR CCs 中增强的胞吐作用。然而,电子显微镜未显示 SHR 和 WKY 大鼠肾上腺髓质之间颗粒大小有显着差异。尽管如此,preSHR 和 hypSHR 的颗粒比 WKY 多 63%和 82%,这可以部分解释增强的儿茶酚胺分泌。导致高血压前期 SHR CC 异质群体和偏向分泌更多中大和大颗粒的机制仍未得到解释。