Dieguez G, Gómez B, Lluch S
Stroke. 1980 Jul-Aug;11(4):372-6. doi: 10.1161/01.str.11.4.372.
The effects of diazoxide on cerebral blood flow were evaluated in unanesthetized goats under control conditions and after selective blockade of adrenergic or cholinergic receptors in cerebral vessels. Injections of diazoxide (1-27 mg) into the internal maxillary artery produced dose-dependent increases in cerebral blood flow, an increase of 90% occurring with the highest dose. Administration of phentolamine, propranolol, or atropine into the internal maxillary artery did not modify the cerebrovascular response to diazoxide. In reserpine-treated animals the cerebral effects of diazoxide were also unchanged. Intravenous injections of diazoxide (150-400 mg) produced sustained hypotension and tachycardia whereas cerebral blood flow was maintained within normal values or increased slightly. The normal cerebral vasoconstriction obtained with injections of norepinephrine directly into the internal maxillary artery was unaffected during the diazoxide induced-hypotension. These findings show that diazoxide exerts a powerful vasodilatory effect on cerebral vessels through mechanisms other than blockade of alpha-adrenergic receptors or inhibition of adrenergic activity. The results also indicate that activation of beta-adrenergic or atropine-sensitive vascular receptors in the cerebral response to diazoxide is negligible.
在对照条件下以及在选择性阻断脑血管中的肾上腺素能或胆碱能受体后,对未麻醉的山羊评估了二氮嗪对脑血流量的影响。向内上颌动脉注射二氮嗪(1 - 27毫克)可使脑血流量产生剂量依赖性增加,最高剂量时增加90%。向内上颌动脉注射酚妥拉明、普萘洛尔或阿托品不会改变脑血管对二氮嗪的反应。在利血平处理的动物中,二氮嗪的脑效应也未改变。静脉注射二氮嗪(150 - 400毫克)会导致持续性低血压和心动过速,而脑血流量维持在正常范围内或略有增加。在二氮嗪诱导的低血压期间,直接向内上颌动脉注射去甲肾上腺素所产生的正常脑血管收缩不受影响。这些发现表明,二氮嗪通过阻断α - 肾上腺素能受体或抑制肾上腺素能活性以外的机制对脑血管发挥强大的血管舒张作用。结果还表明,在二氮嗪引起的脑反应中,β - 肾上腺素能或阿托品敏感的血管受体的激活可忽略不计。