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血管加压素可增加肾小球系膜细胞胞质内的游离钙浓度。

Vasopressin increases cytosolic free calcium concentration in glomerular mesangial cells.

作者信息

Bonventre J V, Skorecki K L, Kreisberg J I, Cheung J Y

出版信息

Am J Physiol. 1986 Jul;251(1 Pt 2):F94-102. doi: 10.1152/ajprenal.1986.251.1.F94.

Abstract

Cytosolic free calcium concentration ([Ca2+]f) was determined in cultured rat glomerular mesangial cells under basal conditions and after exposure to arginine vasopressin (AVP) or angiotensin II (ANG II). [Ca2+]f was determined using quin 2 or fura-2, two intracellular fluorescent probes. [Ca2+]f was measured to be 102 +/- 3 nM (n = 154) using quin 2 and 82 +/- 4 (n = 34) using fura-2. AVP and ANG II increased [Ca2+]f. Maximal levels of [Ca2+]f were achieved in less than 10 s after addition of the hormone. This peak value was followed by a rapid fall toward the base line. With fura-2 as the intracellular Ca2+ indicator, [Ca2+]f increased from 74 +/- 7 to a peak of 578 +/- 39 nM (n = 17) with 100 nM AVP. At 115 s after addition of AVP, [Ca2+]f was 125 +/- 9 nM. Similar peak levels of [Ca2+]f were observed using quin 2. The increase in [Ca2+]f was due in large part to release of Ca2+ from intracellular stores, since reduction in extracellular free [Ca2+] with EGTA did not prevent the hormone-induced increase in [Ca2+]f, although it did result in a decreased peak level and a more rapid return to base line. The AVP-induced increase in [Ca2+]f was blocked by the V1 receptor antagonist (CH2)5Tyr(Me)VDAVP. Neither isoproterenol, which increased adenylate cyclase activity, nor dibutyryl cAMP had any affect on [Ca2+]f directly or on the AVP-induced increase in [Ca2+]f. In this report we present the first direct measurements of [Ca2+]f and hormone-induced changes in [Ca2+]f in glomerular mesangial cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在基础条件下以及暴露于精氨酸加压素(AVP)或血管紧张素II(ANG II)后,测定培养的大鼠肾小球系膜细胞中的胞质游离钙浓度([Ca2+]f)。使用两种细胞内荧光探针喹啉2或fura-2来测定[Ca2+]f。使用喹啉2测得[Ca2+]f为102±3 nM(n = 154),使用fura-2测得为82±4(n = 34)。AVP和ANG II可增加[Ca2+]f。添加激素后不到10秒就达到了[Ca2+]f的最高水平。该峰值之后迅速降至基线。以fura-2作为细胞内Ca2+指示剂,100 nM AVP可使[Ca2+]f从74±7增加至峰值578±39 nM(n = 17)。添加AVP后115秒时,[Ca2+]f为125±9 nM。使用喹啉2也观察到了类似的[Ca2+]f峰值水平。[Ca2+]f的增加很大程度上是由于细胞内储存的Ca2+释放,因为用乙二醇双四乙酸(EGTA)降低细胞外游离[Ca2+]并不能阻止激素诱导的[Ca2+]f增加,尽管这确实导致峰值水平降低且更快恢复到基线。AVP诱导的[Ca2+]f增加被V1受体拮抗剂(CH2)5Tyr(Me)VDAVP阻断。增加腺苷酸环化酶活性的异丙肾上腺素和二丁酰环磷腺苷对[Ca2+]f或AVP诱导的[Ca2+]f增加均无直接影响。在本报告中,我们首次直接测量了肾小球系膜细胞中的[Ca2+]f以及激素诱导的[Ca2+]f变化。(摘要截短至250字)

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