Ndisang Joseph Fomusi, Wang Rui
Department of Physiology, University of Saskatchewan, Saskatchewan, Canada, S7N 5E5.
Exp Biol Med (Maywood). 2003 May;228(5):557-63. doi: 10.1177/15353702-0322805-27.
Enhancement of the heme oxygenase/carbon monoxide (HO/CO) system has been shown to lower blood pressure (BP) in young (8 weeks), but not in adult (20 weeks) spontaneously hypertensive (SHR) rats. The reasons for this selective effect still remain puzzling. We investigated the effects of hemin on the HO/CO system of the pulmonary artery (PA) in SHR and Wistar-Kyoto (WKY) rats at different ages and evaluated the hemin-dependent changes in sGC and cGMP pathways. Hemin administration resulted in an evident reduction of BP (from 148.6 +/- 3.2 to 125.8 +/- 2.6 mmHg, P < 0.01) in young, but not in prehypertensive (4 weeks) or adult SHR or WKY rats at all ages. Coadministration of the HO inhibitor, chromium mesoporphyrin, with hemin, cancelled the BP-lowering effect of hemin. Remarkably, lower expression levels of HO-1, HO-2, and sGC paralleled with reduced HO activity and cGMP content were observed in PA from 8-week SHR rats, but not from adult SHR or WKY rats of all ages. Interestingly, hemin treatment restored these deficiencies, although the expression level of non-inducible HO-2 protein remained unchanged. We conclude that in young and prehypertensive SHR rats, an impaired HO/CO-sGC/cGMP system in the PA might be indicative of the pathogenesis and development of hypertension. In contrast, the HO/CO system in the PA of adult SHR rats was upregulated as a compensatory reaction to elevated BP and desensitization of the downstream targets of the sGC/cGMP pathway occurred.
已表明增强血红素加氧酶/一氧化碳(HO/CO)系统可降低年轻(8周龄)自发性高血压(SHR)大鼠的血压(BP),但对成年(20周龄)SHR大鼠无效。这种选择性作用的原因仍然令人费解。我们研究了血红素对不同年龄SHR大鼠和Wistar-Kyoto(WKY)大鼠肺动脉(PA)的HO/CO系统的影响,并评估了血红素依赖性的可溶性鸟苷酸环化酶(sGC)和环磷酸鸟苷(cGMP)途径的变化。给予血红素可使年轻SHR大鼠的血压明显降低(从148.6±3.2 mmHg降至125.8±2.6 mmHg,P<0.01),但对所有年龄的高血压前期(4周龄)或成年SHR大鼠和WKY大鼠均无此作用。HO抑制剂中卟啉铬与血红素共同给药可消除血红素的降压作用。值得注意的是,在8周龄SHR大鼠的PA中观察到HO-1、HO-2和sGC的表达水平较低,同时HO活性和cGMP含量降低,但在所有年龄的成年SHR大鼠或WKY大鼠中未观察到这种情况。有趣的是,尽管非诱导性HO-2蛋白的表达水平保持不变,但血红素治疗恢复了这些缺陷。我们得出结论,在年轻和高血压前期SHR大鼠中,PA中受损的HO/CO-sGC/cGMP系统可能指示高血压的发病机制和发展。相比之下,成年SHR大鼠PA中的HO/CO系统上调,作为对血压升高的代偿反应,并且sGC/cGMP途径的下游靶点发生脱敏。