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嘌呤能激动剂对大鼠下颌下腺锌摄取的调节作用。

Regulation by purinergic agonists of zinc uptake by rat submandibular glands.

作者信息

Dehaye J P

机构信息

Laboratoire de Biochimie générale et humaine, Université libre de Bruxelles, Belgium.

出版信息

J Trace Elem Med Biol. 1995 Jul;9(2):94-101. doi: 10.1016/S0946-672X(11)80017-9.

Abstract

The zinc uptake in rat submandibular cells was measured using fura2 as a fluorescent probe. Basal zinc uptake was observed in a 100 microM - 1 mM concentration range. Carbachol and isoproterenol had no effect but ATP4- dose-dependently increased the basal zinc uptake (half-maximal concentration: 250 microM). The purinergic agonist shifted the concentration curve for zinc to the left by one order of magnitude. The response to ATP was not reproduced by adenosine or ADP and was blocked by Coomassie blue. Calcium, nickel or lanthanum were inhibitors of zinc uptake, while the substitution of extracellular sodium by potassium or lithium increased the basal zinc uptake. We conclude that in submandibular cells zinc can permeate through the non-specific cation channel coupled to ATP-sensitive purinergic receptors.

摘要

使用fura2作为荧光探针测量大鼠下颌下腺细胞中的锌摄取。在100微摩尔 - 1毫摩尔的浓度范围内观察到基础锌摄取。卡巴胆碱和异丙肾上腺素没有作用,但ATP4-剂量依赖性地增加基础锌摄取(半数最大浓度:250微摩尔)。嘌呤能激动剂使锌的浓度曲线向左移动一个数量级。腺苷或ADP不能重现对ATP的反应,且该反应被考马斯亮蓝阻断。钙、镍或镧是锌摄取的抑制剂,而用钾或锂替代细胞外钠会增加基础锌摄取。我们得出结论,在下颌下腺细胞中,锌可以通过与ATP敏感嘌呤能受体偶联的非特异性阳离子通道渗透。

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