Sausbier M, Schubert R, Voigt V, Hirneiss C, Pfeifer A, Korth M, Kleppisch T, Ruth P, Hofmann F
Institut für Pharmakologie und Toxikologie der TU München, München, Germany.
Circ Res. 2000 Oct 27;87(9):825-30. doi: 10.1161/01.res.87.9.825.
Both cGMP-dependent and -independent mechanisms have been implicated in the regulation of vascular tone by NO. We analyzed acetylcholine (ACh)- and NO-induced relaxation in pressurized small arteries and aortic rings from wild-type (wt) and cGMP kinase I-deficient (cGKI(-/-)) mice. Low concentrations of NO and ACh decreased the spontaneous myogenic tone in wt but not in cGKI(-/-) arteries. However, contractions of cGKI(-/-) arteries and aortic rings were reduced by high concentrations (10 micromol/L) of 2-(N:, N-diethylamino)-diazenolate-2-oxide (DEA-NO). Iberiotoxin, a specific blocker of Ca(2+)-activated K(+) (BK(Ca)) channels, only partially prevented the relaxation induced by DEA-NO or ACh in pressurized vessels and aortic rings. DEA-NO increased the activity of BK(Ca) channels only in vascular smooth muscle cells isolated from wt cGKI(+/+) mice. These results suggest that low physiological concentrations of NO decrease vascular tone through activation of cGKI, whereas high concentrations of DEA-NO relax vascular smooth muscle independent of cGKI and BK(Ca). NO-stimulated, cGKI-independent relaxation was antagonized by the inhibition of soluble guanylyl cyclase or cAMP kinase (cAK). DEA-NO increased cGMP to levels that are sufficient to activate cAK. cAMP-dependent relaxation was unperturbed in cGKI(-/-) vessels. In conclusion, low concentrations of NO relax vessels by activation of cGKI, whereas in the absence of cGKI, NO can relax small and large vessels by cGMP-dependent activation of cAK.
cGMP依赖性和非依赖性机制均参与了一氧化氮(NO)对血管张力的调节。我们分析了野生型(wt)和cGMP激酶I缺陷型(cGKI(-/-))小鼠的加压小动脉和主动脉环中乙酰胆碱(ACh)和NO诱导的舒张情况。低浓度的NO和ACh可降低wt小鼠动脉的自发性肌源性张力,但对cGKI(-/-)动脉无效。然而,高浓度(10 μmol/L)的2-(N,N-二乙氨基)-重氮酸酯-2-氧化物(DEA-NO)可降低cGKI(-/-)动脉和主动脉环的收缩。伊贝毒素是一种Ca(2+)激活的K(+)(BK(Ca))通道特异性阻滞剂,仅部分阻止了DEA-NO或ACh在加压血管和主动脉环中诱导的舒张。DEA-NO仅在从wt cGKI(+/+)小鼠分离的血管平滑肌细胞中增加BK(Ca)通道的活性。这些结果表明,生理浓度的低浓度NO通过激活cGKI降低血管张力,而高浓度的DEA-NO可独立于cGKI和BK(Ca)使血管平滑肌舒张。NO刺激的、不依赖cGKI的舒张可被可溶性鸟苷酸环化酶或cAMP激酶(cAK)的抑制所拮抗。DEA-NO使cGMP增加到足以激活cAK的水平。cAMP依赖性舒张在cGKI(-/-)血管中不受影响。总之,低浓度的NO通过激活cGKI使血管舒张,而在缺乏cGKI时,NO可通过cGMP依赖性激活cAK使小血管和大血管舒张。