Matsuura M, Kamura M, Muneoka Y
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1983;76(2):305-11. doi: 10.1016/0742-8413(83)90083-x.
The effects of alpha-adrenoceptor agonists and antagonists on contractions of the ABRM of M. edulis were examined. Naphazoline (10(-11)-10(-7)M) as well as octopamine potentiated both contractions in response to ACh and to repetitive electrical stimulation with brief pulses, while clonidine (10(-12)-10(-6)M), imidazole (10(-4)-10(-3)M) and tolazoline (10(-6)-10(-4)M) potentiated only the contraction in response to repetitive electrical stimulation. Potentiating actions of octopamine and naphazoline on ACh contraction were blocked by tolazoline but were little affected by clonidine and imidazole. Potentiating after-effect of repetitive electrical stimulation on subsequent ACh-contraction was not affected by clonidine and imidazole but was blocked by tolazoline. These results suggest that in the ABRM there are probably at least two classes of alpha-like receptors for octopamine; one may be on the muscle fibres and the other may be on the excitatory nerve terminals. Activation of the latter class of receptors may result in enhancement of ACh release from the terminals.
研究了α-肾上腺素能受体激动剂和拮抗剂对贻贝前闭壳肌(ABRM)收缩的影响。萘甲唑啉(10⁻¹¹ - 10⁻⁷M)以及章鱼胺增强了对乙酰胆碱(ACh)的收缩反应和对短脉冲重复电刺激的收缩反应,而可乐定(10⁻¹² - 10⁻⁶M)、咪唑(10⁻⁴ - 10⁻³M)和妥拉唑啉(10⁻⁶ - 10⁻⁴M)仅增强了对重复电刺激的收缩反应。章鱼胺和萘甲唑啉对ACh收缩的增强作用被妥拉唑啉阻断,但受可乐定和咪唑的影响较小。重复电刺激对随后ACh收缩的增强后效应不受可乐定和咪唑的影响,但被妥拉唑啉阻断。这些结果表明,在ABRM中可能至少有两类对章鱼胺呈α样反应的受体;一类可能位于肌纤维上,另一类可能位于兴奋性神经末梢上。后一类受体的激活可能导致神经末梢ACh释放增加。