Sphingosine inhibits muscarinic cholinergic receptor binding in rat parotid acinar cells.

Y Fujita, H Sugiya
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Abstract

1. Sphingosine inhibited the binding of [3H]quinuclidinyl benzilate (QNB), a potent and specific muscarinic antagonist, in dispersed rat parotid acinar cells. 2. The inhibition of [3H]QNB binding was expressed as decrease in affinity without significant change of a number of membrane sites. 3. The effect of sphingosine on the binding was not affected by the chelation of extracellular Ca2+. 4. H-7, an inhibitor of protein kinase C, failed to decrease [3H]QNB binding. 5. Stearylamine, an analogue of sphingosine, was as effective as sphingosine in inhibiting [3H]QNB binding. 6. These results suggest that sphingosine inhibits muscarinic cholinergic receptor binding by a mechanism that is independent on extracellular Ca2+ and protein kinase C.

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鞘氨醇抑制大鼠腮腺腺泡细胞毒蕈碱胆碱能受体结合。
1. Sphingosine抑制了[3H]quinuclidinyl benzilate (QNB)在分散的大鼠腮腺腺泡细胞中的结合,QNB是一种有效的特异性毒蕈碱拮抗剂。2. 对[3H]QNB结合的抑制表现为亲和力降低,但一些膜位点没有明显变化。3.鞘氨醇对结合的影响不受细胞外Ca2+螯合的影响。4. 蛋白激酶C抑制剂H-7未能降低[3H]QNB结合。5. 硬脂胺是鞘氨醇的类似物,在抑制[3H]QNB结合方面与鞘氨醇一样有效。6. 这些结果表明鞘氨醇通过一种独立于细胞外Ca2+和蛋白激酶C的机制抑制毒蕈碱胆碱能受体结合。
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