Mechanism of Taiwan Mingjian Oolong Tea to Inhibit Isoproterenol-Induced Hypertrophy and Apoptosis in Cardiomyoblasts

Author:

Yeh Yu-Lan12,Tsai Hsiang-I3,Cheng Shiu-Min4,Pai Peiying5,Ho Tsung-Jung67,Chen Ray-Jade8,Lai Chao-Hung9,Huang Pei-Jane10,Padma V. Vijaya11,Huang Chih-Yang3107

Affiliation:

1. Department of Pathology, Changhua Christian Hospital, Changhua, Taiwan

2. Department of Medical Technology, Jen-Teh Junior College of Medicine, Nursing and Management, Miaoli, Taiwan

3. Graduate Institute of Basic Medical Science, Taichung, Taiwan

4. Department of Psychology, Asia University, Taichung, Taiwan

5. Division of Cardiology, China Medical University Hospital, Taichung, Taiwan

6. School of Chinese Medicine, China Medical University, Taichung, Taiwan

7. Chinese Medicine Department, China Medical University Beigang Hospital, Taiwan

8. Department of Surgery, School of Medicine, College of Medicine, Taipei Medical University, Taipei, Taiwan

9. Division of Cardiology, Department of Internal Medicine, Armed Force Taichung General Hospital, Taichung, Taiwan

10. Department of Health and Nutrition Biotechnology, Asia University, Taichung, Taiwan

11. Department of Biotechnology, Bharathiar University, Coimbatore 641046, India

Abstract

This study investigates the cardio-protective effect of Nos. 1 and 5 extracts from Taiwan Mingjian Oolong Tea on H9c2 cardiomyoblast cells treated with isoproterenol (ISO). Treatment with Nos. 1 and 5 extracts increased cell viability and blocked apoptosis in ISO exposed H9c2 cells. Moreover, Nos. 1 and 5 extracts blocked hypertrophy markers like G[Formula: see text]s, calcineurin, NFATc3, and BNP, thereby increasing cell proliferation markers -PI3K and AKT in a dose dependent manner. In contrast, apoptotic proteins, such as caspase-3 and cytochrome c were decreased in H9c2 cells treated with Nos. 1 and 5 extracts. We confirmed that the protective effect of No. 1 extract was partially mediated through the expression of ERK and p38, however, the No. 5 extract showed a protective effect via the ERK, JNK, and p38 pathways. This evidence provides new insights into the pharmacological role and therapeutic mechanism of Taiwan Mingjian Oolong Tea in heart diseases.

Publisher

World Scientific Pub Co Pte Lt

Subject

Complementary and alternative medicine,General Medicine

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