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Caffeine-mediated alleviation of imbalance of calcium homeostasis and apoptosis in cardiomyocytes caused by RyR2 knockdown
Received date: 2025-10-09
Revised date: 2026-03-06
Accepted date: 2026-03-06
Online published: 2026-06-27
Objective This study aims to investigate the effects of low-concentration caffeine on calcium homeostasis and apoptosis in rat cardiomyocytes with ryanodine receptor 2 (RyR2) knockdown. Methods Neonatal Sprague-Dawley (SD) rats of specific pathogen-free (SPF) grade were used, and neonatal rat ventricular myocytes (NRVMs) were isolated and extracted. Synthetic small interfering RNA (siRNA) targeting RyR2 and the negative control (NC) were transfected into NRVMs, and the cells were divided into four groups: NC group (transfected with siRNA NC), siRyR2 group (transfected with RyR2 siRNA), NC+caffeine group (0.2 mmol/L caffeine added after siRNA NC transfection), and siRyR2+caffeine group (0.2 mmol/L caffeine added after RyR2 siRNA transfection). The mRNA and protein expression levels of RyR2 were detected by quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot. Cell apoptosis and calcium ions were detected by flow cytometry, and free calcium ion concentration was detected by confocal calcium ion imaging. Data from the NC, siRyR2, NC+caffeine, and siRyR2+caffeine groups were analyzed by one-way analysis of variance. Results Compared with the NC group, the mRNA and protein expression levels of RyR2 in the siRyR2 group were significantly decreased (mRNA: 0.41±0.04 vs 1.00±0.09, P=0.000 3; protein: 0.34±0.04 vs 0.72±0.02, P=0.000 1), calcium ion concentration was significantly decreased (flow cytometry: 0.80±0.02 vs 1.00±0.02, P<0.000 1; confocal: 61.08%±0.75% vs 100.00%±2.33%, P<0.000 1), and the apoptosis rate was significantly increased (9.21%±0.07% vs 4.19%±0.07%, P<0.000 1). In the NC+caffeine group, the mRNA and protein expression levels of RyR2 were significantly increased (mRNA: 1.27±0.15 vs 1.00±0.09, P=0.033 6; protein: 0.92±0.10 vs 0.72±0.02, P=0.006 5), calcium ion concentration was significantly increased (flow cytometry: 01.33±0.04 vs 1.00±0.02, P<0.000 1; confocal: 116.21%±1.51% vs 100.00%±2.33%, P=0.000 6), and the apoptosis rate was significantly decreased (2.97%±0.13% vs 4.19%±0.07%, P<0.000 1). Compared with the siRyR2 group, the mRNA and protein expression levels of RyR2 in the siRyR2+caffeine group were significantly increased (mRNA: 0.67±0.08 vs 0.41±0.04, P=0.044 7; protein: 0.54±0.01 vs 0.34±0.04, P=0.009 1), calcium ion concentration was significantly increased (flow cytometry: 0.87±0.02 vs 0.80±0.02, P=0.026 3; confocal: 79.14%±5.02% vs 61.08%±0.75%, P=0.000 3), and the apoptosis rate was significantly decreased (7.59%±0.10% vs 9.21%±0.07%, P<0.000 1). Compared with the NC+caffeine group, the mRNA and protein expression levels of RyR2 in the siRyR2+caffeine group were significantly decreased (mRNA: 0.67±0.08 vs 1.27±0.15, P=0.000 2; protein: 0.54±0.01 vs 0.92±0.10, P<0.000 1), calcium ion concentration was significantly decreased (flow cytometry: 0.87±0.02 vs 1.33±0.04, P<0.000 1; confocal: 79.14%±5.02% vs 116.21%±1.51%, P<0.000 1), and the apoptosis rate was significantly increased (7.59%±0.10% vs 2.97%±0.13%, P<0.000 1). Conclusions Low-concentration caffeine can promote calcium ion release, restore calcium homeostasis, and reduce apoptosis by upregulating RyR2 in cardiomyocytes. This interaction mechanism between caffeine and RyR2 can provide a reference for the development of therapeutic drugs for heart diseases such as arrhythmias caused by decreased RyR2 expression.
YE Yuanzheng , FU Xiaoxiao , MEN Li , MA Qiancheng , ZHANG Andi , FAN Ping . Caffeine-mediated alleviation of imbalance of calcium homeostasis and apoptosis in cardiomyocytes caused by RyR2 knockdown[J]. Journal of Diagnostics Concepts & Practice, 2026 , 25(03) : 346 -353 . DOI: 10.16150/j.1671-2870.2026.03.011
| [1] | SECCO I, GIACCA M. Regulation of endogenous cardiomyocyte proliferation: The known unknowns[J]. J Mol Cell Cardiol, 2023,179:80-89. |
| [2] | KAUR S, BHATTI G K, KHULLAR N, et al. Calcium signalling and organelle crosstalk in cardiovascular disease: An interplay of cardiac cell death pathways[J]. Mol Biol Rep, 2025, 52(1):907. |
| [3] | REDEL-TRAUB G, MARX S O, MARKS A R. Targeting calcium regulation for heart failure and arrhythmia therapeutics: A critical review[J]. Circulation, 2025, 152(13):957-970. |
| [4] | XING Y, CUI T, SUN F. A novel RyR2 mutation associated with co-morbid catecholaminergic polymorphic ventricular tachycardia (CPVT) and benign epilepsy with centrotemporal spikes (BECTS)[J]. J Electrocardiol, 2024,84:75-80. |
| [5] | 丁宣尹, 雷迁. 兰尼碱受体2在心脏疾病中的研究现状[J]. 实用医院临床杂志, 2024, 21(3):181-184. |
| DING X Y, LEI Q. Current status of RyR2 research in heart disease[J]. Pract J Clin Med, 2024, 21(3):181-184. | |
| [6] | DO T Q, KNOLLMANN B C. Inhibitors of intracellular RyR2 calcium release channels as therapeutic agents in arrhythmogenic heart diseases[J]. Annu Rev Pharmacol Toxicol, 2025,65:443-463. |
| [7] | FUJII S, KOBAYASHI S, CHANG Y, et al. RyR2-targe-ting therapy prevents left ventricular remodeling and ventricular tachycardia in post-infarction heart failure[J]. J Mol Cell Cardiol, 2023,178:36-50. |
| [8] | KOBAYASHI S, YAMAMOTO T, YANO M. RyR2-stabilization therapy with dantrolene against left ventricular remodeling and lethal arrhythmia in heart failure[J]. J Mol Cell Cardiol, 2023,182:25-27. |
| [9] | KAPLAN A D, BOYMAN L, WARD C W, et al. Ryanodine receptor stabilization therapy suppresses Ca2+- based arrhythmias in a novel model of metabolic HFpEF[J]. J Mol Cell Cardiol, 2024,195:68-72. |
| [10] | MARKS A R. Targeting ryanodine receptors to treat human diseases[J]. J Clin Investig, 2023, 133(2):e162891. |
| [11] | EHRLICH B E, KAFTAN E, BEZPROZVANNAYA S, et al. The pharmacology of intracellular Ca2+-release channels[J]. Trends Pharmacol Sci, 1994, 15(5):145-149. |
| [12] | 王伟, 李莎, 张梦丹, 等. liguzinediol基于肌浆网钙泵促进钙释放发挥正性肌力作用[J]. 中国药理学与毒理学杂志, 2016, 30(3):197-202. |
| WANG W, LI S, ZHANG M D, et al. Liguzinediol exerts positive inotropic effect by enhancing Ca 2+release from sarcoplasmic reticulum mediated by sarcoplasmic reticulum Ca2+ATPase[J]. Chin J Pharmacol Toxicol, 2016, 30(3):197-202. | |
| [13] | 李博, 吴慧颖, 朴虎林, 等. 新生大鼠心肌细胞原代培养方法的改良[J]. 中国实验诊断学, 2012, 16(2):200-203. |
| LI B, WU H Y, PIAO H L, et al. The primary culture of neonatal rat cardiac cells[J]. Chin J Lab Diagn, 2012, 16(2):200-203. | |
| [14] | GAIDAI O, CAO Y, LOGINOV S. Global cardiovascular diseases death rate prediction[J]. Curr Probl Cardiol, 2023, 48(5):101622. |
| [15] | CALDWELL J L, CLARKE J D, SMITH C E R, et al. Resto-ring atrial T-tubules augments systolic Ca upon recovery from heart failure[J]. Circ Res, 2024, 135(7):739-754. |
| [16] | BAKER A J, LI O Y, JE?EK F, et al. Ca2+ increases cardiac muscle viscoelasticity independent of active force development[J]. Biophys J, 2025, 124(16):2698-2707. |
| [17] | 秦京京, 武瑞, 韩庆烽. 基于颈动脉粥样硬化标志物的高校职工心血管疾病风险预测模型比较[J]. 中国临床研究, 2026, 39(2):252-256. |
| QIN J J, WU D, HANG Q F. Comparison of cardiovascular disease risk prediction models in university staff based on carotid atherosclerosis biomarker[J]. Chin J Clin Res, 2026, 39(2):252-256. | |
| [18] | LV T, LI S, LI Q, et al. The role of RyR2 mutations in congenital heart diseases: Insights into cardiac electrophysiological mechanisms[J]. Cardiovasc Electrophysiol, 2025, 36(3):683-692. |
| [19] | STARNES L, HALL A, ETAL D, et al. RYR2 deficient human model identifies calcium handling and metabolic dysfunction impacting pharmacological responses[J]. Front Cardiovasc Med, 2024,11:1357315. |
| [20] | DEWLAND T A, VAN DAM R M, MARCUS G M. Coffee and cardiovascular disease[J]. Eur Heart J, 2025, 46(36):3546-3554. |
| [21] | 王明, 王春丽, 张永正. 心肌细胞凋亡信号通路在心肌梗死中的作用及其研究进展[J]. 安徽医学, 2026, 47(5):648-652. |
| WANG M, WANG C L, ZHANG Y Z. The role and research progress of cardiomyocyte apoptosis signaling pathway in myocardial infarction[J]. Anhui Med, 2026, 47(5):648-652. | |
| [22] | 邓洁, 刘晓明, 卢微. 中青年营养状况与冠心病的关系[J]. 中华全科医学, 2025, 23(11):1834-1837. |
| DENG J, LIU X M, LU W. The relationship between nutritional status and coronary atherosclerotic heart disease in young and middle-aged people[J]. Chin J Gen Pract, 2025, 23(11):1834-1837. | |
| [23] | CAMPAGNA R, VIGNINI A. The role of xenobiotic caffeine on cardiovascular health: Promises and challenges[J]. JoX, 2025, 15(2):51. |
| [24] | MüLLER C E, DALY J W. Stimulation of calcium release by caffeine analogs in pheochromocytoma cells[J]. Biochem Pharmacol, 1993, 46(10):1825-1829. |
| [25] | SHKRYL V M. The spatio-temporal properties of calcium transients in hippocampal pyramidal neurons in vitro[J]. Front Cell Neurosci, 2022,16:1054950. |
| [26] | CHOI K J, JEON W Y, LEE M Y, et al. Histamine-induced cytosolic calcium mobilization in human bronchial smooth muscle cells[J]. J Smooth Muscle Res, 2025,61:29-42. |
| [27] | LEE C, DENNETT A M, PINSON J A, et al. Caffeine consumed prior to cardiac stress testing may affect diagnostic accuracy of nuclear medicine myocardial imaging of myocardial ischemia: A systematic review and meta-analysis[J]. J Med Imag Radiat Sci, 2024, 55(1):134-145. |
| [28] | LIU B, ZHU X, ZHOU Q, et al. Activating ryanodine receptor improves isoflurane-induced cognitive dysfunction[J]. Brain Res Bull, 2023,204:110790. |
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