Crocin, a carotenoid component of Crocus cativus, exerts inhibitory effects on L-type Ca2+ current, Ca2+ transient, and contractility in rat ventricular myocytes

Author:

Liu Tao1,Chu Xi2,Wang Hua1,Zhang Xuan3,Zhang Yuanyuan3,Guo Hui3,Liu Zhenyi3,Dong Yongsheng4,Liu Hongying5,Liu Yang1,Chu Li13,Zhang Jianping13

Affiliation:

1. Hebei Medical University, No. 361, East Zhongshan Road, Shijiazhuang 050017, Hebei, China.

2. The Fourth Hospital of Hebei Medical University, No. 12, Jiankang Road, Shijiazhuang 050011, Hebei, China.

3. Hebei University of Chinese Medicine, No. 3, Xingyuan Road, Shijiazhuang 050200, Hebei, China.

4. Intensive Care Unit, Air Force General Hospital, No. 30, Fucheng Road, Haidian 100142, Beijing, China.

5. Department of Infectious Diseases, Hebei General Hospital, Shijiazhuang, Hebei 050051, Shijiazhuang, China.

Abstract

Crocin, a carotenoid component of Crocus sativus L. belonging to the Iridaceae family, has demonstrated cardioprotective effects. To investigate the cellular mechanisms of these cardioprotective effects, here we studied the influence of crocin on L-type Ca2+current (ICa-L), intracellular Ca2+ ([Ca2+]i), and contraction of isolated rat cardiomyocytes by using the whole-cell patch-clamp technique and video-based edge detection and dual excitation fluorescence photomultiplier systems. Crocin inhibited ICa-L in a concentration-dependent manner with the half-maximal inhibitory concentration (IC50) of 45 μmol/L and the maximal inhibitory effect of 72.195% ± 1.54%. Neither current–voltage relationship of ICa-L, reversal potential of ICa-L, nor the activation/inactivation of ICa-L was significantly changed. Crocin at 1 μmol/L reduced cell shortening by 44.64% ± 2.12% and the peak value of the Ca2+ transient by 23.66% ± 4.52%. Crocin significantly reduced amplitudes of myocyte shortening and [Ca2+]i with an increase in the time to reach 10% of the peak (Tp) and a decrease in the time to 10% of the baseline (Tr). Thus, the cardioprotective effects of crocin may be attributed to the attenuation of [Ca2+]i through the inhibition of ICa-L in rat cardiomyocytes and negative inotropic effects on myocardial contractility.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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