Effects of palmatine on potassium and calcium currents in isolated rat hepatocytes

被引:29
作者
Wang, F [1 ]
Zhou, HY
Cheng, L
Zhao, G
Zhou, J
Fu, LY
Yao, WX
机构
[1] Huazhong Univ Sci & Technol, Dept Pharmacol, Tongji Med Coll, Wuhan 430030, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Union Hosp, Dept Pancreat Surg Ctr, Tongji Med Coll, Wuhan 430022, Hubei, Peoples R China
关键词
D O I
10.3748/wjg.v9.i2.329
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To study the effects of palmatine, a known inhibitor on delayed rectifier potassium current and L-type calcium current (I-Ca,I-L) in guinea pig ventricular myocytes, on the potassium and calcium currents in isolated rat hepatocytes. METHODS: Tight-seal whole-cell patch-clamp techniques were performed to investigate the effects of palmatine on the delayed outward potassium currents (I-K), inward rectifier potassium current (I-K1) and Ca2+ release-activated Ca2+ current (I-CRAC) in enzymatically isolated rat hepatocytes. RESULTS: Palmatine 0.3-100 muM reduced IK in a concentration-dependent manner with EC50 of 41.62+/-10.11 muM and n(H), 0.48+/-0.07 (n=8). The effect of the drug was poorly reversible after washout. When the bath solution was changed to tetraethylammonium (TEA) 8 MM, I-K was inhibited. Palmatine 10 muM and 100 muM shifted the I-V curves Of IK downward, and the block Of IK was voltage-independent. Palmatine 0.3-100 muM also inhibited I-CRAC in a concentration-dependent manner. The fitting parameters were as follows: EC50=51.19+/-15.18 muM, and n(H)=0.46+/-0.07 (n=8). The peak value of I-CRAC in the I-V relationship was decreased by palmatine 10 muM and 100 muM But the reverse potential of I-K I-CRAC occurred at Voltage=0 mV in all cells. Palmatine 0.3-100 muM failed to have any significant effect on either inward or outward components Of I-K1 at any membrane potential examined. CONCLUSION: The inhibitory effects on I-K and I-CRAC could be one of the mechanisms that palmatine exerts protective effect on hepatocytes.
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页码:329 / 333
页数:5
相关论文
共 42 条
[1]   Inhibition of chemical carcinogenesis by berberine in rats and mice [J].
Anis, KV ;
Rajeshkumar, NV ;
Kuttan, R .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (05) :763-768
[2]   REGULATION OF CA-2+ EFFLUX IN RAT-LIVER MITOCHONDRIA - ROLE OF MEMBRANE-POTENTIAL [J].
BERNARDI, P ;
AZZONE, GF .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1983, 134 (02) :377-383
[3]   Effects of tetrabutylhydroperoxide on hepatocyte ion channels [J].
Breit, S ;
Kolb, HA ;
Häussinger, D ;
Lang, F .
CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 1999, 9 (03) :133-138
[4]   Effects of palmatine on isometric force and intracellular calcium levels of arterial smooth muscle [J].
Chang, YL ;
Usami, S ;
Hsieh, MT ;
Jiang, MJ .
LIFE SCIENCES, 1999, 64 (08) :597-606
[5]   Inhibition of calcium influx during hypoxia/reoxygenation in primary cultured rat hepatocytes [J].
Crenesse, D ;
Hugues, M ;
Ferre, C ;
Poiree, JC ;
Benoliel, J ;
Dolisi, C ;
Gugenheim, J .
PHARMACOLOGY, 1999, 58 (03) :160-170
[6]  
Cui GY, 1999, ACTA PHARMACOL SIN, V20, P415
[7]   Energetics of swelling in isolated hepatocytes:: A comprehensive study [J].
Devin, A ;
Espié, P ;
Guérin, B ;
Rigoulet, M .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1998, 184 (1-2) :107-121
[8]  
Einarsson C, 2000, WORLD J GASTROENTERO, V6, P522
[9]   Evidence that 2-aminoethyl diphenylborate is a novel inhibitor of store-operated Ca2+ channels in liver cells, and acts through a mechanism which does not involve inositol trisphosphate receptors [J].
Gregory, RB ;
Rychkov, G ;
Barritt, GJ .
BIOCHEMICAL JOURNAL, 2001, 354 :285-290
[10]   Differential inhibitory effects of carbon tetrachloride on the hepatic plasma membrane, mitochondrial and endoplasmic reticular calcium transport systems: implications to hepatotoxicity [J].
Hemmings, SJ ;
Pulga, VB ;
Tran, ST ;
Uwiera, RRE .
CELL BIOCHEMISTRY AND FUNCTION, 2002, 20 (01) :47-59