Nadaud S, Mao C, Luvàra G, Michel J B, Soubrier F
INSERM U358, Hôpital Saint-Louis, Paris, France.
J Hypertens. 1998 Sep;16(9):1315-23. doi: 10.1097/00004872-199816090-00013.
The roles of nitric oxide synthases (NOS) in kidney function are still controversial, principally due to the lack of isoform-specific inhibitors of NOS.
To investigate the relative roles of each isoform of NOS in regulation of sodium and volume homeostasis.
We studied the effects of long-term modifications of sodium diet and blood pressure on expression of NOS mRNA in the renal cortex, where the three isoforms of NOS are present.
We used quantitative reverse-transcription-polymerase chain reaction assays specific to each isoform of NOS to determine amounts of their respective mRNA in control rats, deoxycorticosterone acetate (DOCA)-salt hypertensive rats, rats fed a high-salt diet, and furosemide-treated rats fed a low-sodium diet. Nicotinamide adenine nucleotide phosphate H (NADPH) diaphorase staining was performed on DOCA-salt and control rat kidneys.
Levels of NOS I mRNA in DOCA-salt rats were decreased by treatment, those in low-salt-diet rats remained unaffected and those in high-salt diet rats tended to be intermediate between those of the other rat groups. Expression of NOS III mRNA was not significantly modified by either treatment Levels of NOS II mRNA in DOCA-salt rats were increased, those in high-salt-diet rats remained unaffected, and those in low-salt-diet were decreased by treatment, but these levels are more than 100-fold lower than those observed for the other isoforms of NOS. NADPH diaphorase staining in macula densa of DOCA-salt rats was markedly decreased compared with that in macula densa of control rats but staining in renal inflammatory and fibrous lesions became detectable, and staining in the vessels did not differ from that for control rats.
Our results show that intake of sodium and extracellular fluid volume regulate levels of mRNA of the three NOS isoforms in the renal cortex differently, suggesting that each of them plays a specific role.
一氧化氮合酶(NOS)在肾脏功能中的作用仍存在争议,主要原因是缺乏 NOS 同工型特异性抑制剂。
研究 NOS 各同工型在调节钠和容量稳态中的相对作用。
我们研究了长期改变钠饮食和血压对肾皮质中 NOS mRNA 表达的影响,肾皮质中存在 NOS 的三种同工型。
我们使用针对 NOS 各同工型的定量逆转录-聚合酶链反应分析,来确定对照大鼠、醋酸脱氧皮质酮(DOCA)-盐高血压大鼠、高盐饮食大鼠以及呋塞米治疗的低钠饮食大鼠中各自 mRNA 的量。对 DOCA-盐大鼠和对照大鼠的肾脏进行烟酰胺腺嘌呤二核苷酸磷酸 H(NADPH)黄递酶染色。
DOCA-盐大鼠中 NOS I mRNA 的水平经治疗后降低,低盐饮食大鼠中的水平未受影响,高盐饮食大鼠中的水平倾向于介于其他大鼠组之间。NOS III mRNA 的表达未因任何一种治疗而发生显著改变。DOCA-盐大鼠中 NOS II mRNA 的水平升高,高盐饮食大鼠中的水平未受影响,低盐饮食大鼠中的水平经治疗后降低,但这些水平比 NOS 其他同工型所观察到的水平低 100 倍以上。与对照大鼠致密斑中的 NADPH 黄递酶染色相比,DOCA-盐大鼠致密斑中的染色明显减少,但在肾脏炎症和纤维病变中可检测到染色,血管中的染色与对照大鼠无异。
我们的结果表明,钠的摄入和细胞外液容量对肾皮质中三种 NOS 同工型 mRNA 水平的调节方式不同,提示它们各自发挥特定作用。