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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Growth hormone interferes with the progression of myocarditis in rats.
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Growth hormone interferes with the progression of myocarditis in rats.

机译:生长激素干扰大鼠心肌炎的进展。

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摘要

In this study, we investigated whether recombinant human growth hormone (rhGH) influences the progression of myocarditis. We induced experimental autoimmune myocarditis in F344 rats by subcutaneous injection of cardiac myosin, and divided the rats into three groups: (1) control group, saline injection; (2) pre-treated group, subcutaneous injection of rhGH (100 mIU/rat/day for 10 days) before induction of experimental autoimmune myocarditis; and (3) post-treated group, subcutaneous injection of rhGH (100 mIU/rat/day for 10 days) after induction of experimental autoimmune myocarditis. On the 35th day after induction of experimental autoimmune myocarditis, all rats were sacrificed and the hearts were examined. The increase in body weight was smaller in the control group than the pre-treated group and the rate of heart weight/body weight was larger in the control group than in the two treated groups. Histopathologically, rats in the control group showed multifocal infiltration by inflammatory cells, mainly neutrophils, lymphocytes and macrophages, extensive fibrosis, and a higher proportion of mast cells in the inflamed region. In contrast, rats in the two treated groups showed only minor changes. We found that rhGH did not influence the distribution of lymphocytes in peripheral blood in the three groups, and that rhGH induced G1 checkpoint dysfunction, thereby arresting the cell cycle in G1 and inhibiting the proliferation of mast cells in vitro. These findings suggest a possible role for mast cells in the progression of myocarditis and the rhGH may be a candidate for use as a new tool to treat myocarditis.
机译:在这项研究中,我们调查了重组人生长激素(rhGH)是否影响心肌炎的进展。我们通过皮下注射心肌肌球蛋白诱导F344大鼠实验性自身免疫性心肌炎,并将大鼠分为三组:(1)对照组,生理盐水注射; (2)预处理组,在诱导实验性自身免疫性心肌炎之前,皮下注射rhGH(100mIU /大鼠/天,共10天); (3)后处理组,在诱导实验性自身免疫性心肌炎后皮下注射rhGH(100mIU /大鼠/天,共10天)。在实验性自身免疫性心肌炎诱导后第35天,处死所有大鼠并检查心脏。对照组中的体重增加小于预处理组,并且对照组中的心重/体重的比率大于两个治疗组。在组织病理学上,对照组的大鼠表现出炎症细胞多灶性浸润,主要是中性粒细胞,淋巴细胞和巨噬细胞,广泛的纤维化以及发炎区域肥大细胞的比例更高。相反,两个治疗组中的大鼠仅表现出较小的变化。我们发现rhGH不会影响三组中外周血淋巴细胞的分布,并且rhGH会诱导G1检查点功能异常,从而阻止G1中的细胞周期并抑制体外肥大细胞的增殖。这些发现表明肥大细胞可能在心肌炎的进展中发挥作用,而rhGH可能会被用作治疗心肌炎的新工具。

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