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. 2024 Jul 2;19:93. doi: 10.1186/s13020-024-00936-8

Table 5.

The mechanisms of allicin in myocardial fibrosis

Research model Model establishment Intervention methods Drug effects Main molecular mechanisms Citation
Wistar male rats with diabetic cardiomyopathy Single injection of 65 g/kg streptozotocin intraperitoneally 40 mg/kg gavage for 4 weeks Alleviating cardiac dysfunction, decreasing myocardium fibrosis

⬇ LVEDD, LVESD, NF-κB p65, p-NF-κB p65

⬆ LVEF, FS, E/A

[19]
Wistar rats with MI Ligating LAD 1.2, 1.8, and 3.6 mg/kg, intraperitoneal injection for 3 weeks Alleviating myocardial fibrosis

⬇ Collagen I, collagen III, TGF-β, Smad3

⬆ Smad7

[67]
Male Wistar rats with Diabetes mellitus Single intraperitoneal injection of streptozotocin, 40 mg/kg after overnight fast 4, 8, and 16 mg/kg were given by intraperitoneal injection Reducing myocardial damage, improving cardiac function

⬇ Blood glucose, Fas, TGF-β1, CTGF, Ca2+, LVEDP, − dp/dtmax

⬆ Bcl-2, LVSP, + dp/dtmax

[68]

Bcl-2 b-cell lymphoma-2, CTGF connective tissue growth factor, FAS factor related apoptosis, LVEDD left ventricular end-diastolic dimension, LVEDP left ventricular end-diastolic pressure, LVESD left ventricular end-systolic internal diameter, LVSP left ventricular systolic pressure, LVW/BW left ventricle weight to body weight ratio, LVPWd left ventricular posterior wall diastolic thicknesses, LVSP left ventricular systolic pressure, TGF-β transforming growth factor-β, ± dp/dtmax maximum rate of the left ventricular pressure rise and fall