Key result
Tannic acid blocks L-type Ca2+ current in rat ventricular myocytes by up to ~46%.
Why the study?
The effects of tannic acid on the L-type Ca(2+) current of cardiomyocytes remain undefined.
Does tannic acid affect L-type calcium channels and contractility in rat ventricular myocytes?
Does tannic acid affect L-type calcium channels and contractility in rat ventricular myocytes?
Tannic acid inhibits L-type calcium channels and reduces contractility in rat ventricular myocytes, providing experimental evidence for its cellular mechanism of action.
Tannic acid blocks L-type Ca channels in rat myocytes; leaves open any effects on contractility or relevance to human therapy.
Tannic acid (TA) is a group of water-soluble polyphenolic compounds that occur mainly in plant-derived feeds, food grains and fruits. Many studies have explored its biomedical properties, such as anticancer, antibacterial, antimutagenic, antioxidant, antidiabetic, antiinflammatory and antihypertensive activities. However, the effects of TA on the L-type Ca(2+) current (ICa-L) of cardiomyocytes remain undefined. The present study examined the effects of TA on ICa-L using the whole-cell patch-clamp technique and on intracellular Ca(2+) handling and cell contractility in rat ventricular myocytes with the aid of a video-based edge detection system. Exposure to TA resulted in a concentration- and voltage-dependent blockade of ICa-L, with the half maximal inhibitory concentration of 1.69 μM and the maximal inhibitory effect of 46.15%. Moreover, TA significantly inhibited the amplitude of myocyte shortening and peak value of Ca(2+) transient and increased the time to 10% of the peak. These findings provide new experimental evidence for the cellular mechanism of action of TA and may help to expand clinical treatments for cardiovascular disease.
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Zhu et al. (2016) studied this question. Tannic acid was evaluated on L-type Ca(2+) current (ICa-L). Tannic acid produced a concentration- and voltage-dependent blockade of L-type Ca2+ current in rat ventricular myocytes, with an IC50 of 1.69 μM and a maximal inhibitory effect of 46.15%.
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