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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2006, Vol. 11 ›› Issue (5): 485-490.

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Effects of N-n-butyl haloperidol iodide on intracellular calcium in rat car-diomyocytes

HUANG Zhan-qin, SHI Gang-gang, GAO Fen-fei, ZHOU Yan-qiong, ZHANG Yan-mei, LIU Xin-ping   

  1. Department of Pharmacology, Medical College of ShantouUniversity, Shantou 515041, Guangdong, China
  • Received:2006-03-03 Revised:2006-04-15 Online:2006-05-26 Published:2020-12-09

Abstract: AIM: To investigate the effects of N-n-benzyl haloperidol iodide (F2) on intracellular calcium ([ Ca2+ ]i) in rat cardiomyocytes.METHODS: Cardio-myocytes were loadedwith Fluo3-AM, a calcium sensitive fluorescent dye, and the[ Ca2+ ]i was determined by the use of laser scanning confocal microscope (LSCM).RESULTS:In the Tyrode' s solution with Ca2+ at the con-centration of 1.8 mmol·L-1, 60 mmol·L-1 KCl induced a rapid increase of intracellular calcium fluorescence in-tensity (FI).The FI was increased from the basic value (1.0) to 1.84±0.35 (P<0.01, n =50).With prein-cubation of cardiomyocytes with F2 0.1, 1, 10 μmol·L-1, the FI elevation was inhibited in a concentra-tion-dependent manner.The calculated IC50 was 1.61 μmol·L-1.F2 also reduced the FI elevated by 60 mmol·L-1 KCl in a concentration dependent manner.The FI was decreased by 0.1、1、10μmol·L-1 F2 from 1.92± 0.42(n =50) to 1.88 ±0.39(P >0.05, n =50), 1.31 ±0.36(P<0.01, n =50), 1.09 ±0.05(P<0.01, n =50), respectively.The calculated IC50 was 1.78 μmol·L-1.F2 had no effects of on[ Ca2+ ]i in the resting state, and had no effects on intracellular calcium release induced by caffeine and inositol-1, 4, 5-trisphosphate. CONCLUSION: F2 reduces[ Ca2+ ]i.via inhibition of voltage dependent calcium channel, which is possibly in-volved in the mechanism of its protective effects on myo-cardial ischemia reperfusion injury.

Key words: haloperidol, cardiomyocytes, calcium, laser scanning confocal microscopy

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