de Jong W, Petty M
J Cardiovasc Pharmacol. 1982;4 Suppl 1:S77-80. doi: 10.1097/00005344-198200041-00016.
The cardiovascular effects of catecholamines and related substances after local application into the nucleus tractus solitarii (NTS) of the medulla oblongata of urethane anesthetized rats are summarized. The catecholamines in the nanomolar dose range appear to activate stereospecifically receptor sites in the NTS, resulting in a decrease in blood pressure. Bradycardia occurs after bilateral administration of higher doses. The type of catecholaminergic receptors involved is discussed on the basis of the effects of different catecholamine receptor stimulating agents and pharmacological blockade. Both alpha-methylnoradrenaline and alpha-methyladrenaline are active and it is concluded that they both may contribute to the antihypertensive action of alpha-methyldopa. It is probable that an alpha-type of receptor mediates these hypotensive effects in the NTS. The nature of this receptor needs further characterization.
总结了在氨基甲酸乙酯麻醉大鼠的延髓孤束核(NTS)局部应用儿茶酚胺及相关物质后的心血管效应。纳摩尔剂量范围内的儿茶酚胺似乎能特异性激活NTS中的受体位点,导致血压下降。双侧给予较高剂量后会出现心动过缓。根据不同儿茶酚胺受体激动剂和药理学阻断的作用,讨论了所涉及的儿茶酚胺能受体类型。α-甲基去甲肾上腺素和α-甲基肾上腺素均有活性,得出的结论是它们都可能有助于α-甲基多巴的降压作用。很可能是α型受体介导了NTS中的这些降压作用。该受体的性质需要进一步表征。