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Protective effects of beef decoction rich in carnosine on cerebral ischemia injury by permanent middle cerebral artery occlusion in rats.
Wang, Ai-Hong; Ma, Qian; Wang, Xin; Xu, Gui-Hua.
Afiliação
  • Wang AH; Department of Basic Nursing, Institute of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.
  • Ma Q; Department of Basic Nursing, Institute of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.
  • Wang X; Department of Basic Nursing, Institute of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.
  • Xu GH; Department of Chinese Medicine Nursing, Institute of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu 210023, P.R. China.
Exp Ther Med ; 15(2): 1321-1329, 2018 Feb.
Article em En | MEDLINE | ID: mdl-29399121
ABSTRACT
Inflammation has a role in the cerebral injury induced by ischemia and the present study aimed to determine the mechanism of the protective effect of beef decoction (BD) with carnosine against it. A rat model of permanent middle cerebral artery occlusion was established using a suture method in the vehicle and each of the BD groups. In experiment 1, 72 Sprague Dawley (SD) rats were randomly divided into three groups Sham, vehicle and BD-treated group. Rats in the BD group were given 600 mg/kg BD by oral gavage for 1, 3 and 7 days. The sham and vehicle group rats received an equivalent amount of normal saline. In experiment 2, 60 SD rats were randomly divided into six groups Sham-operated I, sham-operated II, vehicle, low-dose BD, medium-dose BD and high-dose BD group. Rats in the low-, medium- and high-dose BD groups were given BD at the dose of 200, 400 and 600 mg/kg, respectively, by oral gavage for 7 days. Rats in the sham-operated II group were given 600 mg/kg BD. Rats in the sham-operated I group and vehicle group were given the same volume of normal saline by oral gavage. The body weight, neurological deficits and infarct volume were recorded at 1, 3 and 7 days after the operation. Furthermore, the effect of different doses of BD on interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), interferon-γ (IFN-γ) and interleukin-4 (IL-4) levels in peripheral blood was measured at 7 days. BD-treated rats showed less neurological deficits and a smaller infarct volume at 7 days. BD at 400 and 600 mg/kg significantly decreased the infarct volume in rats. At 600 mg/kg BD, a decline in IL-6, TNF-α, IFN-γ and an increase in IL-4 expression was observed in the BD groups, while no difference in body weight and neurological dysfunction was detected. In conclusion, BD is a neuroprotective agent that may be used as a supplement treatment of ischemic stroke.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2018 Tipo de documento: Article