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一氧化氮参与钙介导的肾素释放调节。

Nitric oxide participates in calcium-mediated regulation of renin release.

作者信息

Beierwaltes W H

机构信息

Division of Hypertension and Vascular Research, Henry Ford Hospital, Detroit, MI 48202-2689.

出版信息

Hypertension. 1994 Jan;23(1 Suppl):I40-4. doi: 10.1161/01.hyp.23.1_suppl.i40.

Abstract

The regulation of renin release is unusual in that intracellular calcium reportedly acts as an inhibitory second messenger. Increased calcium not only inhibits renin release but is a cofactor in nitric oxide synthesis. Also, nitric oxide can inhibit renin release. This study was done in vitro using rat renal cortical slices to determine whether calcium-mediated renin inhibition could be in part due to the concurrent production of nitric oxide. Renin concentration in the incubation medium was determined by radioimmunoassay for angiotensin I (Ang I) generation (in nanograms Ang I per hour per milligram per 30 minutes of incubation). In all studies, n = 6 to 17. In normal-calcium incubation medium (2.6 mmol/L), 10(-4) mol/L NG-monomethyl L-arginine, which blocks nitric oxide synthesis, caused an 18% increase in basal renin release (78.6 +/- 8.9 versus 66.7 +/- 5.8 [ng Ang I/h]/mg per 30 minutes incubation, P < .05). When calcium was eliminated from the incubation medium, basal renin release doubled (to 133.1 +/- 15.2 [ng Ang I/h]/mg per 30 minutes incubation, P < .001). Without calcium, inhibiting nitric oxide synthesis had no further effect on renin release (126.8 +/- 17.7 [ng Ang I/h]/mg per 30 minutes incubation). High-calcium medium (7.8 mmol/L) reduced basal renin release by half (30.8 +/- 4.8 [ng Ang I/h]/mg per 30 minutes incubation, P < .001), but inhibiting nitric oxide synthesis in high-calcium medium stimulated renin release by 50% (46.9 +/- 6.2 [ng Ang I/h]/mg per 30 minutes incubation, P < .005). Addition of the calmodulin inhibitor W-7 completely reversed the inhibition of renin by high-calcium medium.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

肾素释放的调节较为特殊,据报道细胞内钙作为一种抑制性第二信使发挥作用。钙增加不仅抑制肾素释放,还是一氧化氮合成的辅助因子。此外,一氧化氮可抑制肾素释放。本研究采用大鼠肾皮质切片进行体外实验,以确定钙介导的肾素抑制是否部分归因于一氧化氮的同时产生。通过放射免疫分析法测定孵育培养基中肾素浓度,以评估血管紧张素I(Ang I)的生成量(每30分钟孵育每毫克每小时生成的Ang I纳克数)。在所有研究中,n = 6至17。在正常钙浓度的孵育培养基(2.6 mmol/L)中,阻断一氧化氮合成的10(-4) mol/L NG-单甲基L-精氨酸使基础肾素释放增加18%(每30分钟孵育每毫克[78.6 ± 8.9对66.7 ± 5.8 [ng Ang I/h],P <.05)。当从孵育培养基中去除钙时,基础肾素释放增加一倍(至每30分钟孵育每毫克133.1 ± 15.2 [ng Ang I/h],P <.001)。无钙时,抑制一氧化氮合成对肾素释放无进一步影响(每30分钟孵育每毫克126.8 ± 17.7 [ng Ang I/h])。高钙培养基(7.8 mmol/L)使基础肾素释放减少一半(每30分钟孵育每毫克30.8 ± 4.8 [ng Ang I/h],P <.001),但在高钙培养基中抑制一氧化氮合成可使肾素释放增加50%(每30分钟孵育每毫克46.9 ± 6.2 [ng Ang I/h],P <.005)。添加钙调蛋白抑制剂W-7可完全逆转高钙培养基对肾素的抑制作用。(摘要截短于250字)

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