Aortic Arch Constriction-Induced Left Ventricular Hypertrophy Model

Huateng Bio provides TAC-induced LVH models in mice with validated cardiac remodeling. Features microsurgical aortic constriction, echocardiography monitoring, and fibrosis quantification. Ideal for cardiovascular drug development. Download protocols.

Model Name
Aortic Arch Constriction-Induced Left Ventricular Hypertrophy Model
Animal Strains
C57BL/6 Mice

Model Description

Left ventricular hypertrophy (LVH), a hallmark of hypertensive heart disease and a major risk factor for cardiovascular mortality, is replicated through transverse aortic constriction (TAC). Our model mimics human pathophysiology by inducing pressure-overload cardiac remodeling, featuring:

  • Progressive hypertrophy: 40-60% increase in left ventricular mass (LVM)
  • Myocardial fibrosis: Collagen deposition ≥15% (Masson’s Trichrome)
  • Functional decline: Reduced ejection fraction (LVEF ≤45% at 8 weeks)

Key Advantages:
✓ High reproducibility: 90% success rate with microsurgical precision
✓ Controlled disease progression: Adjustable stenosis severity (needle gauge-dependent)
✓ Translational relevance: Validated with antihypertensives (e.g., ACE inhibitors)


Applications

• Anti-hypertensive drug efficacy evaluation
• Myocardial fibrosis therapeutic screening
• Pulmonary hypertension mechanism studies
• Biomarker discovery (NT-proBNP, Galectin-3)


Modeling Protocol —— Microsurgical TAC Procedure

1. Surgical Steps:

  • Anesthetize mice (isoflurane 2-3%) → Midline cervical incision
  • Aortic arch exposure: Isolate between brachiocephalic and left carotid arteries
  • Constriction: Ligate over a 27G needle (0.4mm OD) → Remove needle → 65-70% lumen reduction
  • Close incision with 6-0 sutures

2. Post-op Care: Analgesia (buprenorphine 0.05mg/kg) ∙ Weekly echocardiography


Validation & Testing

Category

Parameters

Hypertrophy Index

Heart weight/tibia length (HW/TL) ∙ LV mass/body weight (LVM/BW)

Histopathology

• H&E: Myocyte cross-sectional area
• Sirius Red: Collagen volume fraction (CVF)

Echocardiography

LVEF ∙ FS ∙ LV wall thickness ∙ E/A ratio

Doppler Hemodynamics

Aortic velocity-time integral (VTI) ∙ Peak gradient (mmHg)

 


Technical Advantages

Feature

TAC Model

Alternative Models

Pressure Gradient Control

Needle gauge-adjusted stenosis

Fixed surgical ligation

Disease Specificity

Pure pressure overload

Volume overload interference

Cost Efficiency

50% lower cost vs genetic models

High transgenic expenses

 


 

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