Alveolar-Bone 发表于 2025-3-25 06:44:24
C. van Kuijk MD PhD,H. K. Genant MDransmission (VT) (Agnati et al., 1986a,b, Agnati et al., 1987; Fuxe et al., 1988). The WT is the classical type of electrochemical transmission, which rests on the physical substrate of the neuronal chain. The VT consists of chemical signals (such as paracrine and endocrine signals), diffusing in th控制 发表于 2025-3-25 09:19:38
Interventional Radiological Techniquesas a potent and irreversible α-adrenergic receptor antagonist. Subsequent . studies in peripheral tissues by Chang et al. (1970) and Kalsner (1973) revealed that it could also irreversibly inactivate muscarinic cholinergic and serotonergic receptors, respectively. There was relatively little interesantiquated 发表于 2025-3-25 12:16:13
https://doi.org/10.1007/978-3-642-60295-5action. Effects on conditioned avoidance responding (CAR) in rats were studied under the same conditions in which in vivo binding of the radioiodinated D. specific benzazepine .I-SCH 38840 was measured. It was found that there is very close agreement between the time-course for antagonism of CAR and孤僻 发表于 2025-3-25 17:41:23
https://doi.org/10.1007/978-3-642-60369-3g changes in basal ganglia output are not yet well defined. These receptors can be divided into different subtypes on the basis of either their pharmacological properties or their location. D-1 and D-2 subtypes have been characterized, as have dopamine cell body autoreceptors, terminal autoreceptorsrefraction 发表于 2025-3-25 21:20:33
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Dopamine D1 and D2 Receptor Selectivities of Agonists and Antagonists, constants for inhibiting the binding of [.H]SCH 23390 at D. receptors (calf caudate nucleus) and at D. receptors (pig anterior pituitary tissue). The most selective agonists were SK&F 38393 (for D.) and (+)-PHNO (for D.), while the most selective antagonists were SCH 23390 (for D.) and raclopride or eticlopride (for D.).离开就切除 发表于 2025-3-26 16:51:38
Advances in Experimental Medicine and Biologyhttp://image.papertrans.cn/c/image/223175.jpg