Beleslin D B, Jovanovic-Micic D, Tomic-Beleslin N
Brain Res Bull. 1987 Mar;18(3):463-5. doi: 10.1016/0361-9230(87)90021-9.
In the unanesthetized cat, TRH was injected into the cerebral ventricles (ICV) through chronically implanted cannulae and the nature of the evoked salivation was investigated. TRH injected in doses from 0.1 to 1.0 mg evoked salivation which was not dose-dependent. The antimuscarinic drug atropine as well as the ganglionic blocking agent mecamylamine injected also ICV prevented the salivation induced by ICV TRH. On the other hand, virtually no effect on the TRH-salivation was induced by the following drugs injected ICV: alpha and the beta adrenergic blocking agents, yohimbine and propranolol; dopamine antagonist, chlorpromazine; 5-hydroxytryptamine antagonist, methysergide; and the antihistamine, antazoline. Further, in cats pretreated with ICV reserpine and 6-hydroxydopamine, but not with ICV 5,6-dihydroxytryptamine and hemicholinium, the salivation caused by ICV TRH was abolished. It is concluded that central cholinoceptive and catecholaminergic mechanisms are involved in the salivation induced by ICV TRH.
在未麻醉的猫身上,通过长期植入的套管将促甲状腺激素释放激素(TRH)注入脑室(ICV),并研究诱发唾液分泌的性质。以0.1至1.0毫克的剂量注射TRH可诱发唾液分泌,且不具有剂量依赖性。同样经脑室注射的抗毒蕈碱药物阿托品以及神经节阻断剂美加明可抑制脑室注射TRH所诱发的唾液分泌。另一方面,以下经脑室注射的药物对TRH诱导的唾液分泌几乎没有影响:α和β肾上腺素能阻断剂、育亨宾和普萘洛尔;多巴胺拮抗剂氯丙嗪;5-羟色胺拮抗剂麦角新碱;以及抗组胺药安他唑啉。此外,在经脑室注射利血平和6-羟基多巴胺预处理的猫中,但未经脑室注射5,6-二羟基色胺和半胱氨酸预处理的猫中,脑室注射TRH所引起的唾液分泌被消除。得出的结论是,中枢胆碱能感受和儿茶酚胺能机制参与了脑室注射TRH所诱发的唾液分泌。