Key result
Leea rubra extract reduces cardiac troponin I and LV weight, improving lipids in hypertrophic mice.
Why the study?
Species of the genus Leea have traditional cardioprotective uses, but their direct effects on the heart remain unreported.
Does crude methanolic extract of Leea rubra leaves reduce cardiac hypertrophy and improve lipid profiles in isoproterenol-induced cardiac hypertrophic mice?
Does crude methanolic extract of Leea rubra leaves reduce cardiac hypertrophy and improve lipid profiles in isoproterenol-induced cardiac hypertrophic mice?
Leea rubra leaves extract showed cardioprotective and antihyperlipidemic effects in a mouse model of isoproterenol-induced cardiac hypertrophy.
Answers are grounded in this paper and cite their sources.
Should not yet change clinical practice in cardiac hypertrophy; hypothesis-generating for herbal antihypertrophic and antihyperlipidemic therapies.
Introduction: Cardiac hypertrophy is a risk factor for many cardiovascular diseases (CVDs). Species of the genus Leea have traditional cardioprotective uses, but their direct effects on the heart remain unreported. This study evaluated the cardioprotective activities of a crude methanolic extract (CME) of L. rubra leaves (LRL) in isoproterenol-induced cardiac hypertrophic mice (IIHM) using atorvastatin as a reference treatment. Methods: IIHM (induced with isoproterenol, 5 mg/kg, 7 days, intraperitoneally) were treated with CME of LRL (40 mg/kg or 80 mg/kg, 28 days, orally) and compared with a standard treatment group (atorvastatin, 20 mg/kg, 28 days, orally) and a negative control group (IIHM, placebo). The cardioprotective and hepatoprotective effects of the extract were evaluated by analysing the changes in blood biochemical parameters, including lipid profile (total cholesterol [TC], triglyceride [TG], high-density lipoprotein [HDL], and low-density lipoprotein [LDL]), cardiac troponin I (CTnI), serum glutamic pyruvic transaminase (SGPT), and serum glutamic oxaloacetic transaminase (SGOT). Analysis was conducted using various commercial test kits. The left ventricular weight and body weight (LVW/BW) ratio was also recorded. Results: LRL significantly improved the lipid profile by lowering TC, TG, and LDL while increasing HDL levels (P<0.0001). Significant cardioprotective (reduced serum CTnI level and LVW/BW ratio (P<0.0001)) and hepatoprotective (reduced serum SGPT and SGOT levels (P<0.0001)) activities were observed in IIHM compared with the negative control group. Conclusion: The present study found antihyperlipidemic, cardioprotective, and hepatoprotective activity after LRL treatment in IIHM. Further investigation is required to identify the compounds and molecular mechanisms responsible for these effects.
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Tushar et al. (2026) studied isoproterenol-induced left ventricular hypertrophy. crude methanolic extract of Leea rubra leaves vs. atorvastatin (20 mg/kg) and placebo was evaluated on lipid profile, cardiac troponin I, SGPT, SGOT, and left ventricular weight to body weight ratio (p=<0.0001). Crude methanolic extract of Leea rubra leaves reduced serum cardiac troponin I, left ventricular weight/body weight ratio, and improved lipid profiles in hypertrophic mice.
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