{"title":"酪氨酸激酶抑制剂对血管平滑肌细胞中Ca2+激活的K+通道活性的调节","authors":"Zhigang Xiong, Ethan Burnette, Donald W. Cheung","doi":"10.1016/0922-4106(95)90023-3","DOIUrl":null,"url":null,"abstract":"<div><p>The effects of the tyrosine kinase inhibitors genistein, lavendustin A, and tyrphostin A25 on Ca<sup>2+</sup>-activated K<sup>+</sup> channel activities in freshly isolated single vascular smooth muscle cells from the rat tail artery were studied by patch clamp recording technique. Genistein (5–50 μM) and lavendustin A (10 μM) increased whole-cell Ca<sup>2+</sup>-activated K<sup>+</sup> channel currents. Increase in single channel activities by genistein and lavendustin A was also observed in excised inside-out patches. Diadzein (15 μM), an inactive analogue of genistein, did not alter channel activities. Tyrphostin A25 (10 nM), which had no significant effect on whole-cell currents in concentrations up to 50 μM, increased the open probability of the channels by 841% in inside-out patches. No potentiation of whole-cell and single channel activities by genistein was observed when ATP was omitted from the intracellular solutions. These observations suggest that tyrosine kinase modulates Ca<sup>2+</sup>-activated K<sup>+</sup> channel activities in vascular smooth muscle cells.</p></div>","PeriodicalId":100502,"journal":{"name":"European Journal of Pharmacology: Molecular Pharmacology","volume":"290 2","pages":"Pages 117-123"},"PeriodicalIF":0.0000,"publicationDate":"1995-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0922-4106(95)90023-3","citationCount":"29","resultStr":"{\"title\":\"Modulation of Ca2+-activated K+ channel activity by tyrosine kinase inhibitors in vascular smooth muscle cell\",\"authors\":\"Zhigang Xiong, Ethan Burnette, Donald W. Cheung\",\"doi\":\"10.1016/0922-4106(95)90023-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The effects of the tyrosine kinase inhibitors genistein, lavendustin A, and tyrphostin A25 on Ca<sup>2+</sup>-activated K<sup>+</sup> channel activities in freshly isolated single vascular smooth muscle cells from the rat tail artery were studied by patch clamp recording technique. Genistein (5–50 μM) and lavendustin A (10 μM) increased whole-cell Ca<sup>2+</sup>-activated K<sup>+</sup> channel currents. Increase in single channel activities by genistein and lavendustin A was also observed in excised inside-out patches. Diadzein (15 μM), an inactive analogue of genistein, did not alter channel activities. Tyrphostin A25 (10 nM), which had no significant effect on whole-cell currents in concentrations up to 50 μM, increased the open probability of the channels by 841% in inside-out patches. No potentiation of whole-cell and single channel activities by genistein was observed when ATP was omitted from the intracellular solutions. These observations suggest that tyrosine kinase modulates Ca<sup>2+</sup>-activated K<sup>+</sup> channel activities in vascular smooth muscle cells.</p></div>\",\"PeriodicalId\":100502,\"journal\":{\"name\":\"European Journal of Pharmacology: Molecular Pharmacology\",\"volume\":\"290 2\",\"pages\":\"Pages 117-123\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-07-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/0922-4106(95)90023-3\",\"citationCount\":\"29\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Pharmacology: Molecular Pharmacology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/0922410695900233\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Pharmacology: Molecular Pharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/0922410695900233","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Modulation of Ca2+-activated K+ channel activity by tyrosine kinase inhibitors in vascular smooth muscle cell
The effects of the tyrosine kinase inhibitors genistein, lavendustin A, and tyrphostin A25 on Ca2+-activated K+ channel activities in freshly isolated single vascular smooth muscle cells from the rat tail artery were studied by patch clamp recording technique. Genistein (5–50 μM) and lavendustin A (10 μM) increased whole-cell Ca2+-activated K+ channel currents. Increase in single channel activities by genistein and lavendustin A was also observed in excised inside-out patches. Diadzein (15 μM), an inactive analogue of genistein, did not alter channel activities. Tyrphostin A25 (10 nM), which had no significant effect on whole-cell currents in concentrations up to 50 μM, increased the open probability of the channels by 841% in inside-out patches. No potentiation of whole-cell and single channel activities by genistein was observed when ATP was omitted from the intracellular solutions. These observations suggest that tyrosine kinase modulates Ca2+-activated K+ channel activities in vascular smooth muscle cells.