Khraibi A A, Norman R A, Dzielak D J
Am J Physiol. 1984 Nov;247(5 Pt 2):H722-6. doi: 10.1152/ajpheart.1984.247.5.H722.
Recent evidence suggests that hypertension in the Okamoto spontaneously hypertensive rat (SHR) may be the result of an autoimmune disorder. To test this hypothesis SHRs were given chronic immunosuppressive therapy (cyclophosphamide). The development of spontaneous hypertension was studied in SHRs receiving cyclophosphamide beginning at age 3 wk. The arterial pressure of the cyclophosphamide-treated SHRs was significantly lower than that of untreated control SHRs once the rats were 8 wk old, and this reduction in blood pressure was maintained for the duration of treatment. Also the effect of chronic immunosuppressive therapy on the maintenance of spontaneous hypertension was determined by beginning treatment in 16-wk-old SHRs. Arterial pressure was significantly less than that of untreated control SHRs after 2 wk of treatment. According to tail-cuff measurements, the level of hypertension in the SHRs was reduced by approximately 50% following 6 wk of immunosuppressive therapy. The mean arterial pressure was significantly reduced after 6 wk to 158 +/- 5.0 mmHg in immunosuppressed SHRs (n = 10) compared with 174 +/- 2.6 mmHg in control SHRs (n = 7). Cyclophosphamide treatment did not have a significant effect on the blood pressure of Wistar or Wistar-Kyoto rats or on the development or maintenance of deoxycorticosterone acetate hypertension. Chronic immunosuppression attenuates hypertension in the Okamoto SHR. These results support the hypothesis that spontaneous hypertension may be due in part to an autoimmune disorder.
最近的证据表明,冈本自发性高血压大鼠(SHR)的高血压可能是自身免疫性疾病的结果。为了验证这一假设,给SHR进行了慢性免疫抑制治疗(环磷酰胺)。从3周龄开始,对接受环磷酰胺治疗的SHR进行自发性高血压发展的研究。一旦大鼠8周龄,经环磷酰胺治疗的SHR的动脉压显著低于未治疗的对照SHR,并且这种血压降低在治疗期间一直维持。此外,通过在16周龄的SHR开始治疗来确定慢性免疫抑制治疗对自发性高血压维持的影响。治疗2周后,动脉压显著低于未治疗的对照SHR。根据尾套测量,免疫抑制治疗6周后,SHR的高血压水平降低了约50%。免疫抑制的SHR(n = 10)在6周后平均动脉压显著降低至158±5.0 mmHg,而对照SHR(n = 7)为174±2.6 mmHg。环磷酰胺治疗对Wistar或Wistar-Kyoto大鼠的血压或醋酸脱氧皮质酮高血压的发展或维持没有显著影响。慢性免疫抑制可减轻冈本SHR的高血压。这些结果支持了自发性高血压可能部分归因于自身免疫性疾病的假设。