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饮食限制对(NZB×NZW)F1小鼠免疫功能和肾脏疾病的影响。

Influence of dietary restriction on immunologic function and renal disease in (NZB x NZW) F1 mice.

作者信息

Fernandes G, Friend P, Yunis E J, Good R A

出版信息

Proc Natl Acad Sci U S A. 1978 Mar;75(3):1500-4. doi: 10.1073/pnas.75.3.1500.

Abstract

In (NZB x NZW)F(1) (B/W) mice, moderate caloric intake [10 kcal (41.8 kJ) per day] from the time of weaning was associated with maintenance of lower body weight, greater capacity of spleen cells to be stimulated with T-cell mitogens, and better preserved capacity to generate cytotoxic cells in response to in vitro and in vivo stimulation with allogeneic tumor cells. Plaque-forming cell response to sheep erythrocytes was also well maintained in animals on the restricted diets when sensitization was accomplished either in vitro or in vivo. Spontaneous suppressor cell activity against plaque-forming cells that developed in controls did not appear in the mice on the restricted diet. Significantly less circulating antibody to native DNA was present in the blood of mice 10 months of age when their dietary intake had been restricted. Histological analysis revealed that the development of renal disease and the deposition of gamma globulin in the glomerular capillaries was markedly inhibited in the mice on restricted diets. Dietary restriction from the time of weaning thus appears to prolong significantly the life of autoimmunity-prone (NZB x NZW)F(1) male and female mice and to alter lymphoid cell immune function, thereby decreasing the autoimmune processes and immunological assault associated with progressive renal disease in these animals.

摘要

在(新西兰黑鼠×新西兰白鼠)F1(B/W)小鼠中,从断奶时起适度的热量摄入[每天10千卡(41.8千焦)]与维持较低体重、脾细胞对T细胞有丝分裂原刺激的更大反应能力以及在体外和体内受到同种异体肿瘤细胞刺激时产生细胞毒性细胞的能力得到更好保存有关。当在体外或体内进行致敏时,限制饮食的动物对绵羊红细胞的空斑形成细胞反应也得到了良好维持。限制饮食的小鼠没有出现对照中出现的针对空斑形成细胞的自发抑制细胞活性。当10月龄小鼠的饮食摄入受到限制时,其血液中天然DNA循环抗体显著减少。组织学分析显示,限制饮食的小鼠肾脏疾病的发展以及γ球蛋白在肾小球毛细血管中的沉积明显受到抑制。因此,从断奶时起进行饮食限制似乎能显著延长易患自身免疫性疾病的(新西兰黑鼠×新西兰白鼠)F1雄性和雌性小鼠的寿命,并改变淋巴细胞免疫功能,从而减少这些动物中与进行性肾脏疾病相关的自身免疫过程和免疫攻击。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9ec/411500/3d5f380cca50/pnas00015-0465-a.jpg

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