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心房利钠肽调节血管紧张素II对曼氏-达比犬肾细胞胞浆中游离钙浓度的影响。

Atrial natriuretic peptide modulates the effect of angiotensin II on the concentration of free calcium in the cytosol of Mandin-Darby canine kidney cells.

作者信息

Nascimento-Gomes G, Souza M O, Vecchia M G, Oshiro M E, Ferreira A T, Mello-Aires M

机构信息

Departamento de Fisiologia, Escola Paulista de Medicina, São Paulo, Brasil.

出版信息

Braz J Med Biol Res. 1995 May;28(5):609-13.

PMID:8555983
Abstract

The effect of angiotensin II (ANG II) and atrial natriuretic peptide (ANP) on intracellular free calcium concentration [Ca2+]i was investigated in Mandin-Darby canine kidney (MDCK) cells in culture. Changes in [Ca2+]i were monitored fluorometrically with the Ca(2+)-sensitive probe fura-2/AM at 37 degrees C using a Perkin-Elmer LS-5 spectrofluorimeter (excitation 340/380 nm, slit 3 nm; emission 520 nm, slit 10 nm). MDCK cells exhibited a mean baseline [Ca2+]i of 98 +/- 10 nM. The addition of increasing concentrations of ANG II (1 pM to 1 microM) to the cell suspension led to a progressive increase in [Ca2+]i to 2-3 times basal levels. In contrast, addition of 1 microM ANP to the cell suspension led to a very rapid 60% decrease in [Ca2+]i. The addition of 1 pM to 1 microM ANG II immediately after 1 microM ANP caused an increase in [Ca2+]i which never exceeded the basal level in the absence of ANP. The data indicate that ANG II increases cell [Ca2+]i, as expected, and provide the new observation that ANP reduces [Ca2+]i in these cells. Furthermore, ANP reduces the increase in [Ca2+]i elicited by ANG II, thus modulating the effect of ANG II on [Ca2+]i.

摘要

在体外培养的犬肾上皮细胞(MDCK)中,研究了血管紧张素II(ANG II)和心房利钠肽(ANP)对细胞内游离钙浓度[Ca2+]i的影响。使用珀金埃尔默LS-5荧光分光光度计(激发波长340/380 nm,狭缝3 nm;发射波长520 nm,狭缝10 nm),在37℃下用Ca(2+)敏感探针fura-2/AM通过荧光法监测[Ca2+]i的变化。MDCK细胞的平均基础[Ca2+]i为98±10 nM。向细胞悬液中加入浓度递增的ANG II(1 pM至1 μM)导致[Ca2+]i逐渐升高至基础水平的2 - 3倍。相反,向细胞悬液中加入1 μM ANP导致[Ca2+]i迅速下降60%。在加入1 μM ANP后立即加入1 pM至1 μM的ANG II,导致[Ca2+]i升高,但从未超过无ANP时的基础水平。数据表明,正如预期的那样,ANG II增加细胞[Ca2+]i,并提供了新的观察结果,即ANP降低这些细胞中的[Ca2+]i。此外,ANP减少ANG II引起的[Ca2+]i升高,从而调节ANG II对[Ca2+]i的作用。

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