Tamaki T, Hasui K, Aki Y, Kimura S, Abe Y
Department of Pharmacology, Kagawa Medical School, Japan.
Jpn J Pharmacol. 1993 Jul;62(3):231-7. doi: 10.1254/jjp.62.231.
We examined the effects of NG-nitro-L-arginine (L-NNA) on isolated rabbit afferent arterioles to confirm that nitric oxide is released at the resistance vessel level in the kidney. We microdissected the superficial afferent arterioles from the kidneys of New Zealand White rabbits. Each afferent arteriole was cannulated with a micropipette system, and the intraluminal pressure was set at 80 mmHg. By our methods, we found that norepinephrine (NE) decreased the lumen diameter of the afferent arterioles in a dose-dependent manner, and acetylcholine increased the lumen diameter of NE-constricted afferent arterioles. L-NNA (10(-4) M) gradually decreased the lumen diameter of afferent arterioles from 21.5 +/- 0.9 to 18.6 +/- 0.9 microns in 20 min, but NG-nitro-D-arginine (10(-4) M) did not affect them (from 21.8 +/- 1.3 to 21.8 +/- 1.5 microns). L-Arginine (10(-2) M) restored the lumen diameter of L-NNA-contracted afferent arterioles to the control levels. These findings indicate that the isolated afferent arteriole has the ability to release or to synthesize and release nitric oxide under basal conditions and that this basal release of nitric oxide plays an important role in the basal tone of the afferent arteriole.
我们研究了NG-硝基-L-精氨酸(L-NNA)对分离的兔传入小动脉的影响,以证实一氧化氮在肾脏阻力血管水平释放。我们从新西兰白兔的肾脏中显微解剖出浅表传入小动脉。每个传入小动脉都用微量移液器系统插管,并将管腔内压力设定为80 mmHg。通过我们的方法,我们发现去甲肾上腺素(NE)以剂量依赖性方式降低传入小动脉的管腔直径,而乙酰胆碱增加NE收缩的传入小动脉的管腔直径。L-NNA(10^(-4) M)在20分钟内逐渐将传入小动脉的管腔直径从21.5±0.9微米降至18.6±0.9微米,但NG-硝基-D-精氨酸(10^(-4) M)对其没有影响(从21.8±1.3微米至21.8±1.5微米)。L-精氨酸(10^(-2) M)将L-NNA收缩的传入小动脉的管腔直径恢复到对照水平。这些发现表明,分离的传入小动脉在基础条件下具有释放或合成并释放一氧化氮的能力,并且这种一氧化氮的基础释放对传入小动脉的基础张力起重要作用。