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Anti-apoptotic and pro-survival effect of alpinate oxyphyllae fructus (AOF) in a D-galactose-induced aging heart

  • Yung Ming Chang
  • , Hen Hong Chang
  • , Wei Wen Kuo
  • , Hung Jen Lin
  • , Yu Lan Yeh
  • , Vijaya Padma Viswanadha
  • , Chin Chuan Tsai
  • , Ray Jade Chen
  • , Hsin Nung Chang
  • , Chih Yang Huang*
  • *Corresponding author for this work
  • I-Shou University
  • E-Da Hospital
  • 1PT Biotechnology Co. Ltd
  • China Medical University Taichung
  • Changhua Christian Hospital
  • Jen-Teh Junior College of Medicine, Nursing and Management
  • Bharathiar University
  • Taipei Medical University
  • Asia University Taiwan

Research output: Contribution to journalJournal Article peer-review

52 Citations (SciVal)

Abstract

Aging, a natural biological/physiological phenomenon, is accelerated by reactive oxygen species (ROS) accumulation and identified by a progressive decrease in physiological function. Several studies have shown a positive relationship between aging and chronic heart failure (HF). Cardiac apoptosis was found in age-related diseases. We used a traditional Chinese medicine, Alpinate Oxyphyllae Fructus (AOF), to evaluate its effect on cardiac anti-apoptosis and pro-survival. Male eight-week-old Sprague-Dawley (SD) rats were segregated into five groups: normal control group (NC), D-Galactose-Induced aging group (Aging), and AOF of 50 (AL (AOF low)), 100 (AM (AOF medium)), 150 (AH (AOF high)) mg/kg/day. After eight weeks, hearts were measured by an Hematoxylin-Eosin (H and E) stain, Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL)-assays and Western blotting. The experimental results show that the cardiomyocyte apoptotic pathway protein expression increased in the D-Galactose-Induced aging groups, with dose-dependent inhibition in the AOF treatment group (AL, AM, and AH). Moreover, the expression of the pro-survival p-Akt (protein kinase B (Akt)), Bcl-2 (B-cell lymphoma 2), anti-apoptotic protein (Bcl-xL) protein decreased significantly in the D-Galactose-induced aging group, with increased performance in the AOF treatment group with levels of p-IGFIR and p-PI3K (Phosphatidylinositol-3’ kinase (PI3K)) to increase by dosage and compensatory performance. On the other hand, the protein of the Sirtuin 1 (SIRT1) pathway expression decreased in the aging groups and showed improvement in the AOF treatment group. Our results suggest that AOF strongly works against ROS-induced aging heart problems.

Original languageEnglish
Article number466
JournalInternational Journal of Molecular Sciences
Volume17
Issue number4
DOIs
StatePublished - 29 03 2016
Externally publishedYes

Bibliographical note

Publisher Copyright:
© 2016 by the authors; licensee MDPI, Basel, Switzerland.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • AOF
  • Apoptosis
  • D-galactose-induced aging
  • SIRT1

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