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n-3多不饱和脂肪酸对巨噬细胞膜磷脂的调节作用可增加白细胞介素1的释放,并防止失血性休克后细胞免疫受到抑制。

Modulation of macrophage membrane phospholipids by n-3 polyunsaturated fatty acids increases interleukin 1 release and prevents suppression of cellular immunity following hemorrhagic shock.

作者信息

Ertel W, Morrison M H, Ayala A, Chaudry I H

机构信息

Department of Surgery, Michigan State University, East Lansing 48824-1315.

出版信息

Arch Surg. 1993 Jan;128(1):15-20; discussion 20-1. doi: 10.1001/archsurg.1993.01420130019004.

DOI:10.1001/archsurg.1993.01420130019004
PMID:8418775
Abstract

Studies have suggested that the significant suppression of cellular immunity following hemorrhage may be due to an increased release of prostaglandin E2 (PGE2) by macrophages. Since diets high in n-3 polyunsaturated fatty acids decrease PGE2 synthesis, we assessed whether hemorrhage-induced immunosuppression could be prevented by dietary manipulation. C3H/HeN mice were fed for 3 weeks with fat sources derived from corn oil, safflower oil, or fish oil, then bled to a mean blood pressure of 35 mm Hg maintained for 60 minutes. Following this, the animals were adequately resuscitated with fluids and killed 24 hours later. In the corn oil and safflower oil groups, hemorrhage resulted in a significant increase in PGE2 release by peritoneal macrophages, a marked suppression of peritoneal macrophage antigen presentation capacity, interleukin 1 release, splenocyte proliferation, and interleukin 2 secretion compared with shams. However, feeding mice with fish oil for 3 weeks prior to hemorrhage prevented the rise in PGE2 release and maintained normal macrophage and splenocyte functions following hemorrhage. Thus, the elevated release of PGE2 by peritoneal macrophages plays a pivotal role in hemorrhage-induced immunosuppression. Moreover, diets high in n-3 polyunsaturated fatty acids may offer a new therapeutic approach for preventing posthemorrhage immunosuppression and increased mortality from sepsis.

摘要

研究表明,出血后细胞免疫的显著抑制可能是由于巨噬细胞释放的前列腺素E2(PGE2)增加所致。由于富含n-3多不饱和脂肪酸的饮食会减少PGE2的合成,我们评估了饮食干预是否可以预防出血诱导的免疫抑制。给C3H/HeN小鼠喂食来自玉米油、红花油或鱼油的脂肪源3周,然后放血至平均血压35 mmHg并维持60分钟。在此之后,用液体对动物进行充分复苏,并在24小时后处死。与假手术组相比,在玉米油和红花油组中,出血导致腹膜巨噬细胞释放的PGE2显著增加,腹膜巨噬细胞抗原呈递能力、白细胞介素1释放、脾细胞增殖和白细胞介素2分泌受到明显抑制。然而,在出血前3周给小鼠喂食鱼油可防止PGE2释放增加,并在出血后维持正常的巨噬细胞和脾细胞功能。因此,腹膜巨噬细胞释放PGE2增加在出血诱导的免疫抑制中起关键作用。此外,富含n-3多不饱和脂肪酸的饮食可能为预防出血后免疫抑制和降低败血症死亡率提供一种新的治疗方法。

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Modulation of macrophage membrane phospholipids by n-3 polyunsaturated fatty acids increases interleukin 1 release and prevents suppression of cellular immunity following hemorrhagic shock.n-3多不饱和脂肪酸对巨噬细胞膜磷脂的调节作用可增加白细胞介素1的释放,并防止失血性休克后细胞免疫受到抑制。
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