Forrest John N
NEW HAVEN, CONNECTICUT.
Trans Am Clin Climatol Assoc. 2016;127:162-175.
The dogfish shark salt gland was predicted by Smith and discovered by Burger at the Mount Desert Island Biological Laboratory in Salisbury Cove, Maine. It is an epithelial organ in the intestine composed of tubules that serve a single function: the secretion of hypertonic NaCl. Many G protein receptors are present on the basolateral surface of these tubules, including stimulatory receptors for vasoactive intestinal peptide, adenosine A, growth hormone releasing hormone, and inhibitory receptors for somatostatin and adenosine A. An entirely different class of stimulatory receptors is present as C-type natriuretic peptide receptors. Each stimulatory receptor evokes powerful NaCl secretion. G protein receptors bind to G to activate the catalytic unit of adenylate cyclase to form cyclic adenosine monophosphate (cAMP) and protein kinase A that phosphorylates the regulatory domain of cystic fibrosis transmembrane conductance regulator, opening the channel. The C-type natriuretic peptide receptor stimulates by activating guanylate cyclase and endogenous cyclic guanosine monophosphate which inhibits type 3 phosphodiesterase, the enzyme that breaks down cAMP, thereby elevating cAMP and activating the protein kinase A pathway.
角鲨的盐腺由史密斯预测,并由伯格在缅因州索尔兹伯里湾的芒特迪瑟特岛生物实验室发现。它是肠道中的一个上皮器官,由具有单一功能的小管组成:分泌高渗氯化钠。这些小管的基底外侧表面存在许多G蛋白受体,包括血管活性肠肽、腺苷A、生长激素释放激素的刺激受体,以及生长抑素和腺苷A的抑制受体。另一类完全不同的刺激受体是C型利钠肽受体。每种刺激受体都会引发强大的氯化钠分泌。G蛋白受体与G结合,激活腺苷酸环化酶的催化单位,形成环磷酸腺苷(cAMP)和蛋白激酶A,蛋白激酶A使囊性纤维化跨膜传导调节因子的调节域磷酸化,打开通道。C型利钠肽受体通过激活鸟苷酸环化酶和内源性环磷酸鸟苷来刺激,内源性环磷酸鸟苷抑制3型磷酸二酯酶,即分解cAMP的酶,从而提高cAMP并激活蛋白激酶A途径。