{"title":"腺苷A1和组胺h1受体之间的相互作用","authors":"John M. Dickenson, Stephen J. Hill","doi":"10.1016/0020-711X(94)90066-3","DOIUrl":null,"url":null,"abstract":"<div><p></p><ul><li><span>1.</span><span><p>1. The interactions or “cross-talk” between adenosine A<sub>1</sub>-receptors and receptors coupled to phospholipase C (leading to the hydrolysis of inositol phospholipids) have been well documented in the literature. For example, activating the A<sub>1</sub>-receptor selectively potentiates the histamine H<sub>1</sub>-receptor stimulated hydrolysis of inositol phospholipids in guinea-pig cerebral slices. In contrast, when the adenosine receptor is activated in the cerebral cortex of mouse or man the histamine response is selectively inhibited.</p></span></li><li><span>2.</span><span><p>2. Our studies have focused on the smooth muscle cell line, DDT<sub>1</sub>MF-2, derived from hamster vas deferens. These cells express A<sub>1</sub>-receptors which, in addition to the expected negative coupling to adenylate cyclase, also stimulate inositol phospholipid hydrolysis and Ca<sup>2+</sup> mobilization. These A<sub>1</sub>-receptors also potentiate histamine H<sub>1</sub>-receptor responses, i.e. inositol phospholipid hydrolysis and Ca<sup>2+</sup> mobilization.</p></span></li><li><span>3.</span><span><p>3. The mechanism(s) underlying the potentiation or inhibition of histamine H<sub>1</sub>-receptor responses by the adenosine A<sub>1</sub>-receptor remain to be unravelled. One mechanism may involve intracellular “cross-talk” at the G-protein level. This review will discuss how βγ subunits from G<sub>1</sub> proteins could be involved in augmenting responses to calcium mobilizing receptors.</p></span></li></ul></div>","PeriodicalId":13733,"journal":{"name":"International Journal of Biochemistry","volume":"26 8","pages":"Pages 959-969"},"PeriodicalIF":0.0000,"publicationDate":"1994-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0020-711X(94)90066-3","citationCount":"36","resultStr":"{\"title\":\"Interactions between adenosine A1- and histamine H1-receptors\",\"authors\":\"John M. Dickenson, Stephen J. Hill\",\"doi\":\"10.1016/0020-711X(94)90066-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p></p><ul><li><span>1.</span><span><p>1. The interactions or “cross-talk” between adenosine A<sub>1</sub>-receptors and receptors coupled to phospholipase C (leading to the hydrolysis of inositol phospholipids) have been well documented in the literature. For example, activating the A<sub>1</sub>-receptor selectively potentiates the histamine H<sub>1</sub>-receptor stimulated hydrolysis of inositol phospholipids in guinea-pig cerebral slices. In contrast, when the adenosine receptor is activated in the cerebral cortex of mouse or man the histamine response is selectively inhibited.</p></span></li><li><span>2.</span><span><p>2. Our studies have focused on the smooth muscle cell line, DDT<sub>1</sub>MF-2, derived from hamster vas deferens. These cells express A<sub>1</sub>-receptors which, in addition to the expected negative coupling to adenylate cyclase, also stimulate inositol phospholipid hydrolysis and Ca<sup>2+</sup> mobilization. These A<sub>1</sub>-receptors also potentiate histamine H<sub>1</sub>-receptor responses, i.e. inositol phospholipid hydrolysis and Ca<sup>2+</sup> mobilization.</p></span></li><li><span>3.</span><span><p>3. The mechanism(s) underlying the potentiation or inhibition of histamine H<sub>1</sub>-receptor responses by the adenosine A<sub>1</sub>-receptor remain to be unravelled. One mechanism may involve intracellular “cross-talk” at the G-protein level. This review will discuss how βγ subunits from G<sub>1</sub> proteins could be involved in augmenting responses to calcium mobilizing receptors.</p></span></li></ul></div>\",\"PeriodicalId\":13733,\"journal\":{\"name\":\"International Journal of Biochemistry\",\"volume\":\"26 8\",\"pages\":\"Pages 959-969\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1994-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0020-711X(94)90066-3\",\"citationCount\":\"36\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Biochemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0020711X94900663\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Biochemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0020711X94900663","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Interactions between adenosine A1- and histamine H1-receptors
1.
1. The interactions or “cross-talk” between adenosine A1-receptors and receptors coupled to phospholipase C (leading to the hydrolysis of inositol phospholipids) have been well documented in the literature. For example, activating the A1-receptor selectively potentiates the histamine H1-receptor stimulated hydrolysis of inositol phospholipids in guinea-pig cerebral slices. In contrast, when the adenosine receptor is activated in the cerebral cortex of mouse or man the histamine response is selectively inhibited.
2.
2. Our studies have focused on the smooth muscle cell line, DDT1MF-2, derived from hamster vas deferens. These cells express A1-receptors which, in addition to the expected negative coupling to adenylate cyclase, also stimulate inositol phospholipid hydrolysis and Ca2+ mobilization. These A1-receptors also potentiate histamine H1-receptor responses, i.e. inositol phospholipid hydrolysis and Ca2+ mobilization.
3.
3. The mechanism(s) underlying the potentiation or inhibition of histamine H1-receptor responses by the adenosine A1-receptor remain to be unravelled. One mechanism may involve intracellular “cross-talk” at the G-protein level. This review will discuss how βγ subunits from G1 proteins could be involved in augmenting responses to calcium mobilizing receptors.