Stachydrine Protects Against Pressure Overload-Induced Cardiac Hypertrophy by Suppressing Autophagy

Tong-Tong Cao1, Hui-Hua Chen1, Zhiwei Dong2

  • 1Department of Pathology, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Insights

Stachydrine, a natural compound, inhibits excessive autophagy and reactive oxygen species (ROS) production by blocking NADPH oxidase 2 (NOX2) activation. This mechanism effectively reduces cardiac hypertrophy in pressure overload heart failure models.

Area of Science:

  • Cardiovascular Research
  • Cellular Biology
  • Pharmacology

Background:

  • Autophagy is crucial for cardiomyocyte health but becomes maladaptive in heart failure.
  • Excessive autophagy contributes to pressure overload-induced cardiac hypertrophy.
  • Understanding Stachydrine's inhibitory mechanisms is key to treating heart failure.

Purpose of the Study:

  • To investigate how Stachydrine inhibits pressure overload-induced cardiac hypertrophy.
  • To determine Stachydrine's effects on NADPH oxidase activation, ROS production, and autophagy.
  • To elucidate the molecular pathways involved in Stachydrine's cardioprotective effects.

Main Methods:

  • Administered Stachydrine to Wistar rats post-Transverse Aortic Constriction (TAC) and to Angiotensin II-stimulated H9c2 cells.
  • Assessed NADPH oxidase 2 (NOX2) activation by measuring p47phox and p67phox translocation via Western blot and immunofluorescence.
  • Quantified intracellular ROS using DCF-DA fluorescence and autophagic flux with mRFP-GFP-LC3 live-cell imaging.

Main Results:

  • Stachydrine inhibited Angiotensin II-induced excessive autophagy in H9c2 cells.
  • Stachydrine blocked p47phox hyperphosphorylation, reduced p47phox/p67phox membrane translocation, and inhibited NOX2 activity.
  • Reduced ROS generation and ameliorated TAC-induced cardiac hypertrophy, dysfunction, and excessive autophagy in vivo.

Conclusions:

  • Regulating NOX2 is critical when autophagy is highly activated.
  • Stachydrine's inhibition of NOX2 reduces ROS production, thereby inhibiting cardiac hypertrophy.
  • These findings suggest Stachydrine has significant potential for clinical application in heart failure treatment.
Abstract

Related Concept Videos

Autophagy01:27

Autophagy

Autophagy is a self-digesting process by which a cell protects itself from threats both within and outside the cell, ranging from abnormal proteins to invading bacteria. In this process, obsolete components of the cell and invading microbes are degraded by hydrolytic enzymes active in an acidic environment of the lysosomal lumen.
An autophagic pathway consists of a series of signaling events activated in response to diverse stress and physiological conditions such as food deprivation,...
6.0K
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
1.3K
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
1.1K
Autophagic Cell Death01:18

Autophagic Cell Death

Christian de Duve discovered “autophagy,” a process in which cellular components are engulfed by membrane-bound organelles called autophagosomes. The autophagosomes then fuse with lysosomes to digest the enclosed contents. Autophagy is generally activated in cells to prevent cell death. However, cell death is triggered when the damage is beyond repair.
Autophagy and Apoptosis
Autophagy can activate apoptosis. In normal conditions, the autophagy activating protein Beclin-1 and...
4.8K
Antihypertensive Drugs: Action of β1 Blockers01:17

Antihypertensive Drugs: Action of β1 Blockers

β1-receptors are primarily located in the heart and kidneys. In cardiac myocytes, these receptors interact with neurotransmitters released by the sympathetic nervous system during heightened activity or danger. As a result, β1-receptors get activated, initiating a series of biochemical processes. Excessive activation of beta receptors due to chronic stress can abnormally increase heart rate and contractility, resulting in high blood pressure or hypertension. To counteract this,...
2.2K
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
1.1K