Nishio H, Segawa T
Jpn J Pharmacol. 1983 Feb;33(1):79-84. doi: 10.1254/jjp.33.79.
Concanavalin A (Con A) was shown to have inhibitory effect on platelet adenylate cyclase as well as 5-hydroxytryptamine (5HT) uptake. These effects of Con A were antagonized by alpha-methyl-D-mannoside, a specific inhibitor of Con A binding to glycoprotein. The effect of Con A on adenylate cyclase was partial inhibition, and Con A had no effect on prostaglandin E1 stimulated activity, indicating the adenylate cyclase which is thought to be involved in 5HT uptake might be a minor component. The same result as Con A was demonstrated in the inhibitory effect of N-ethylmaleimide (NEM) on this activity. Impermeable sulfhydryl blocking reagents and iodoacetamide had no effect on 5HT uptake. It might be necessary for the sulfhydryl blocking reagent to pass through the cell membrane in order to exert its inhibitory effect on 5HT uptake. Furthermore, the inhibitory effect of Con A on 5HT uptake was antagonized by sulfhydryl reducing reagents and adenosine. It is postulated that a NEM sensitive, sub-membrane contractile protein system might mediate the effect of Con A, and Con A might inhibit platelet 5HT uptake by affecting the adenylate cyclase system through some possible transmembrane regulatory mechanism.
伴刀豆球蛋白A(Con A)已被证明对血小板腺苷酸环化酶以及5-羟色胺(5HT)摄取具有抑制作用。Con A的这些作用可被α-甲基-D-甘露糖苷拮抗,α-甲基-D-甘露糖苷是Con A与糖蛋白结合的特异性抑制剂。Con A对腺苷酸环化酶的作用是部分抑制,且Con A对前列腺素E1刺激的活性无影响,这表明被认为参与5HT摄取的腺苷酸环化酶可能是次要成分。在N-乙基马来酰亚胺(NEM)对该活性的抑制作用中也得到了与Con A相同的结果。不能透过细胞膜的巯基阻断剂和碘乙酰胺对5HT摄取无影响。巯基阻断剂可能有必要穿过细胞膜才能对5HT摄取发挥其抑制作用。此外,Con A对5HT摄取的抑制作用可被巯基还原试剂和腺苷拮抗。据推测,一种对NEM敏感的膜下收缩蛋白系统可能介导了Con A的作用,并且Con A可能通过某种可能的跨膜调节机制影响腺苷酸环化酶系统来抑制血小板5HT摄取。