首页> 美国卫生研究院文献>The Journal of Physiology >Muscarinic alpha-adrenergic and peptide receptors regulate the same calcium influx sites in the parotid gland.
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Muscarinic alpha-adrenergic and peptide receptors regulate the same calcium influx sites in the parotid gland.

机译:毒蕈碱α-肾上腺素能和肽受体调节腮腺中相同的钙内流部位。

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摘要

1. Carbachol, phenylephrine and substance P were each capable of producing a transient release of K (86 Rb) from rat parotid slices in the absence of extracellular Ca. 2. Each of the agonists was also capable of producing "cross-receptor inactivation"; that is, if a transient response was elicited by any one of the agonists then no transient response could be obtained by either of the other two. 3. Removal of carbachol from muscarinic receptors with atropine did not reverse the cross-receptor inactivation of the substance P response unless Ca was added with substance P or unless Ca was present when atropine was added. 4. It is concluded that the K release response in the parotid gland is mediated by receptor-controlled Ca influx sites. These influx sites also bind Ca at a location inaccessible to EGTA and release the bound Ca upon receptor activation. 5. It is also conlcuded that all three receptors (muscarinic, alpha-adrenergic, and peptide) appear to regulate the same Ca influx sites.
机译:1.在不存在细胞外钙的情况下,卡巴胆碱,去氧肾上腺素和P物质均能够从大鼠腮腺切片中瞬时释放K(86 Rb)。 2.每种激动剂也能够产生“交叉受体失活”。也就是说,如果任一激动剂引起瞬时反应,则其他两种激动剂均不能获得瞬时反应。 3.用阿托品从毒蕈碱受体中去除卡巴胆碱并不能逆转P物质应答的交叉受体失活,除非Ca与P物质一起添加或当添加阿托品时存在Ca。 4.结论是腮腺中的钾释放反应是由受体控制的Ca流入位点介导的。这些流入位点还在无法到达EGTA的位置结合Ca,并在受体激活后释放结合的Ca。 5.还认为所有三种受体(毒蕈碱,α-肾上腺素和肽)似乎都调节相同的Ca流入位点。

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