Endothelin-1 and photoreleased diacylglycerol increase L-type Ca2+ currentby activation of protein kinase C in rat ventricular myocytes

Citation
Jq. He et al., Endothelin-1 and photoreleased diacylglycerol increase L-type Ca2+ currentby activation of protein kinase C in rat ventricular myocytes, J PHYSL LON, 524(3), 2000, pp. 807-820
Citations number
52
Categorie Soggetti
Physiology
Journal title
JOURNAL OF PHYSIOLOGY-LONDON
ISSN journal
00223751 → ACNP
Volume
524
Issue
3
Year of publication
2000
Pages
807 - 820
Database
ISI
SICI code
0022-3751(200005)524:3<807:EAPDIL>2.0.ZU;2-G
Abstract
1. The amphotericin B-perforated whole-cell patch clamp technique was used to determine the modulation of L-type Ca2+ channels by protein kinase C (PK C)-mediated pathways in adult rat ventricular myocytes. 2. Application of 10 nM endothelin-1 (ET-1) increased peak Ca2+ current (I- Ca) by 28.2 +/- 2.5% (n = 13) and slowed current decay, These effects were prevented by the endothelin receptor antagonist; PD145065 (10 mu M) and by the PKC inhibitor chelerythrine (8 mu M). To establish if direct activation of PKC mimicked the ET-1 effect, the acti ve and inactive phorbol esters (phorbol-12-myristate-13-acetate and 4 alpha -phorbol-12,13-didecanoate) were tested. Both phorbol esters (100 nM) resul ted in a small (similar to 10 %) increase in I-Ca, suggesting PKC-independe nt effects. 4. Bath application of dioctanoylglycerol (diC(8)), a diacylglycerol (DAG) analogue which is capable of directly activating PKC, caused a gradual decl ine in peak I-Ca (50.4 +/- 6.2%, n = 5) and increased the rate of current d ecay. These effects were unaffected by the PKC inhibitor chelerythrine (8 m u M). 5. Intracellular photorelease of caged diC(8) with 3 or 10 s exposure to UV light produced a concentration-dependent increase in peak I-Ca (20.7 +/- 8 .5% (n = 8) for 3 s UV and 60.8 +/- 11.4% (n = 13) for 10 s UV), which coul d be inhibited by chelerythrine. 6. Our results demonstrate that both ET-1 and intracellularly photoreleased diC(8) increase I-Ca by a PKC-mediated pathway which is in direct contrast to the PKC-independent inhibition of I-Ca produced by bath-applied diC(8). We conclude that specific cellular pools of DAG are crucially important; i n the regulation of I-Ca by PKC.