Dooley D J, Bittiger H
J Pharmacol Methods. 1987 Sep;18(2):131-6. doi: 10.1016/0160-5402(87)90005-2.
The use of 100 nM CGP 20712 A (1-[2-((3-carbamoyl-4-hydroxy)phenoxy)ethylamino]-3-[4-(1-methyl-4- trifluoromethyl-2-imidazolyl)phenoxy]-2-propanol methanesulfonate), a specific beta 1-adrenoceptor antagonist, in an in vitro [3H]dihydroalprenolol binding assay simplified the detection of drug-induced alterations in central beta 1- and beta 2-adrenoceptor density. Injection of rats with DSP-4 (N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine hydrochloride), a selective noradrenergic neurotoxin, caused an increase in neocortical and hippocampal beta 1-adrenoceptor density. Subchronic infusion of desipramine, a noradrenaline uptake inhibitor, effected a decrease in neocortical and hippocampal beta 1-adrenoceptor density. Subchronic infusion of clenbuterol, a centrally acting beta-adrenoceptor agonist, appeared to decrease striatal beta 2-adrenoceptor density. The results are discussed in terms of the quantitation and regulation of central beta-adrenoceptors.
在体外[³H]二氢心得舒结合试验中使用100 nM的CGP 20712 A(1-[2-((3-氨基甲酰基-4-羟基)苯氧基)乙氨基]-3-[4-(1-甲基-4-三氟甲基-2-咪唑基)苯氧基]-2-丙醇甲磺酸盐),一种特异性β1-肾上腺素能受体拮抗剂,简化了对药物诱导的中枢β1-和β2-肾上腺素能受体密度变化的检测。给大鼠注射DSP-4(N-(2-氯乙基)-N-乙基-2-溴苄胺盐酸盐),一种选择性去甲肾上腺素能神经毒素,导致新皮质和海马体β1-肾上腺素能受体密度增加。亚慢性输注地昔帕明,一种去甲肾上腺素摄取抑制剂,使新皮质和海马体β1-肾上腺素能受体密度降低。亚慢性输注克仑特罗,一种中枢作用的β-肾上腺素能受体激动剂,似乎使纹状体β2-肾上腺素能受体密度降低。根据中枢β-肾上腺素能受体的定量和调节对结果进行了讨论。