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Morroniside on anti-inflammation activities in rats following acute myocardial infarction
The Korean Journal of Physiology and Pharmacology ; : 17-21, 2018.
Artículo en Inglés | WPRIM | ID: wpr-727942
ABSTRACT
Our previous studies have confirmed that morroniside has neuroprotective effects. However, the effects of morroniside on cardiac myocardium remain unknown. Rats were anaesthetized with 10% chloral hydrate (0.35~0.4 mL/kg) and an acute myocardial infarction (AMI) was induced by ligating the anterior descending coronary artery (LAD). Following AMI, morroniside was administered intragastrically for 3 consecutive days at doses of 45, 90 and 180 mg/kg, respectively. Lactate dehydrogenase (LDH) and cardiac troponin T (cTnT) activities in AMI rats in the serum were detected with commercial kits. The expression of IL-6, IL-1β and TNF-α in myocardium was detected by Western blotting analysis. We observed a significant decline in the Q(q) wave amplitude in morroniside-treated rats after 72 h. Additionally, treatment of morroniside decreased the levels of LDH and cTnT in AMI rats. We also observed that morroniside reduced the expression of IL-6, IL-1β and TNF-α in myocardium. Taken together, our findings demonstrate that morroniside had effective anti-inflammatory properties in AMI rats.
Asunto(s)

Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Hidrato de Cloral / Western Blotting / Interleucina-6 / Fármacos Neuroprotectores / Vasos Coronarios / Troponina T / Inflamación / L-Lactato Deshidrogenasa / Infarto del Miocardio / Miocardio Límite: Animales Idioma: Inglés Revista: The Korean Journal of Physiology and Pharmacology Año: 2018 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Hidrato de Cloral / Western Blotting / Interleucina-6 / Fármacos Neuroprotectores / Vasos Coronarios / Troponina T / Inflamación / L-Lactato Deshidrogenasa / Infarto del Miocardio / Miocardio Límite: Animales Idioma: Inglés Revista: The Korean Journal of Physiology and Pharmacology Año: 2018 Tipo del documento: Artículo