Yamada S, Ishima T, Ashizawa N, Hayashi M, Tomita T, Hayashi E
Brain Res. 1985 Sep 30;344(1):127-33. doi: 10.1016/0006-8993(85)91196-5.
To study potential central adrenoceptor alterations in the hypertension, we have determined alpha 1, alpha 2 and beta-adrenoceptors using [3H]WB4101, [3H]yohimbine and [3H]DHA in the brain regions of spontaneously hypertensive rats (SHR), stroke-prone SHR (SHRSP) and renal hypertensive rats. There was a significant increase in specific [3H]WB4101 binding only in the hypothalamus of SHR and SHRSP at 16-24 weeks of age compared to that of age-matched Wistar-Kyoto rats (WKY). Scatchard analysis revealed a 28-33% increase in the Bmax value for hypothalamic [3H]WB4101 binding without a change in the Kd value, suggesting a change in the receptor density. An increased density of alpha 1-adrenoceptors was consistently observed in the prehypertensive (5 weeks) and developmental (10 weeks) stages of spontaneous hypertension. In contrast, there was no alpha 1-adrenoceptor alteration in the hypothalamus of rats with renal hypertension. The receptor alteration in the SHRSP hypothalamus was not abolished by a chronic hypotensive treatment which prevented the development of hypertension, thereby suggesting that an increased density of the alpha 1-adrenoceptors in spontaneous hypertension does not occur secondarily to the elevation of blood pressure. The SHRSP hypothalamus showed significantly lowered levels of noradrenaline. There was no change in specific binding of [3H]yohimbine and [3H]DHA in the brain regions of SHRSP, except the brainstem which showed a significant decrease in the [3H]yohimbine binding. Thus, the present study suggests an important role for hypothalamic alpha 1-adrenoceptors in the pathogenesis of spontaneous hypertension.
为研究高血压中潜在的中枢肾上腺素能受体改变,我们使用[3H]WB4101、[3H]育亨宾和[3H]二氢麦角隐亭,在自发性高血压大鼠(SHR)、易卒中型SHR(SHRSP)和肾性高血压大鼠的脑区中测定了α1、α2和β肾上腺素能受体。与年龄匹配的Wistar-Kyoto大鼠(WKY)相比,16 - 24周龄的SHR和SHRSP仅在下丘脑中[3H]WB4101的特异性结合显著增加。Scatchard分析显示,下丘脑[3H]WB4101结合的Bmax值增加了28 - 33%,而Kd值无变化,提示受体密度发生改变。在自发性高血压的高血压前期(5周)和发育阶段(10周),始终观察到α1肾上腺素能受体密度增加。相比之下,肾性高血压大鼠的下丘脑未出现α1肾上腺素能受体改变。慢性降压治疗可预防高血压的发生,但并未消除SHRSP下丘脑的受体改变,因此提示自发性高血压中α1肾上腺素能受体密度增加并非继发于血压升高。SHRSP下丘脑的去甲肾上腺素水平显著降低。除脑干中[3H]育亨宾结合显著减少外,SHRSP脑区中[3H]育亨宾和[3H]二氢麦角隐亭的特异性结合无变化。因此,本研究提示下丘脑α1肾上腺素能受体在自发性高血压发病机制中起重要作用。