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巴西区域性基本饮食诱导的慢性营养不良会导致 C57BL6J 小鼠肝脏炎症,并提高载脂蛋白 A-I 的活性。

A Brazilian regional basic diet-induced chronic malnutrition drives liver inflammation with higher ApoA-I activity in C57BL6J mice.

机构信息

Laboratório da Biologia da Cicatrização Tecidual, Ontogenia e Nutrição de Tecidos, Departamento de Morfologia e Instituto de Biomedicina, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE, Brasil.

Núcleo de Microscopia e Processagem de Imagens, Departamento de Morfologia e Instituto de Biomedicina, Faculdade de Medicina, Universidade Federal do Ceará, Fortaleza, CE, Brasil.

出版信息

Braz J Med Biol Res. 2020;53(6):e9031. doi: 10.1590/1414-431x20209031. Epub 2020 May 8.

DOI:10.1590/1414-431x20209031
PMID:32401929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7228546/
Abstract

Malnutrition is still considered endemic in many developing countries. Malnutrition-enteric infections may cause lasting deleterious effects on lipid metabolism, especially in children living in poor settings. The regional basic diet (RBD), produced to mimic the Brazilian northeastern dietary characteristics (rich in carbohydrate and low in protein) has been used in experimental malnutrition models, but few studies have explored the effect of chronic RBD on liver function, a central organ involved in cholesterol metabolism. This study aimed to investigate whether RBD leads to liver inflammatory changes and altered reverse cholesterol metabolism in C57BL6/J mice compared to the control group, receiving a standard chow diet. To evaluate liver inflammation, ionized calcium-binding adapter protein-1 (IBA-1) positive cell counting, interleukin (IL)-1β immunohistochemistry, and tumor necrosis factor (TNF)-α and IL-10 transcription levels were analyzed. In addition, we assessed reverse cholesterol transport by measuring liver apolipoprotein (Apo)E, ApoA-I, and lecithin-cholesterol acyltransferase (LCAT) by RT-PCR. Furthermore, serum alanine aminotransferase (ALT) was measured to assess liver function. RBD markedly impaired body weight gain compared with the control group (P<0.05). Higher hepatic TNF-α (P<0.0001) and IL-10 (P=0.001) mRNA levels were found in RBD-challenged mice, although without detectable non-alcoholic fatty liver disease. Marked IBA-1 immunolabeling and increased number of positive-IBA-1 cells were found in the undernourished group. No statistical difference in serum ALT was found. There was also a significant increase in ApoA mRNA expression in the undernourished group, but not ApoE and LCAT, compared with the control. Altogether our findings suggested that chronic RBD-induced malnutrition leads to liver inflammation with increased ApoA-I activity.

摘要

许多发展中国家仍存在营养不良的问题。营养不良和肠道感染可能会对脂质代谢造成持久的有害影响,尤其是生活在贫困环境中的儿童。区域基本饮食(RBD)旨在模仿巴西东北部的饮食特点(富含碳水化合物,蛋白质含量低),已被用于实验性营养不良模型,但很少有研究探讨慢性 RBD 对肝功能的影响,而肝功能是参与胆固醇代谢的重要器官。本研究旨在探讨 RBD 是否会导致 C57BL6/J 小鼠肝脏发生炎症改变和胆固醇逆向代谢异常,与接受标准饲料的对照组相比。为了评估肝脏炎症,分析了 IBA-1 阳性细胞计数、白细胞介素(IL)-1β免疫组织化学和肿瘤坏死因子(TNF)-α和 IL-10 转录水平。此外,我们通过 RT-PCR 测量了肝脏载脂蛋白(Apo)E、ApoA-I 和卵磷脂胆固醇酰基转移酶(LCAT)来评估胆固醇逆向转运。此外,还测量了血清丙氨酸氨基转移酶(ALT)以评估肝功能。与对照组相比,RBD 明显降低了体重增长(P<0.05)。RBD 组小鼠肝脏 TNF-α(P<0.0001)和 IL-10(P=0.001)mRNA 水平升高,但未发现非酒精性脂肪性肝病。营养不良组 IBA-1 免疫标记明显增加,阳性 IBA-1 细胞数量增加。血清 ALT 无统计学差异。营养不良组 ApoA mRNA 表达显著增加,但 ApoE 和 LCAT 无显著变化。总之,我们的研究结果表明,慢性 RBD 引起的营养不良导致肝脏炎症,ApoA-I 活性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/6dc85d853fde/1414-431X-bjmbr-53-6-e9031-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/3d521313e0b0/1414-431X-bjmbr-53-6-e9031-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/00b3c4506d16/1414-431X-bjmbr-53-6-e9031-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/70d8136835a1/1414-431X-bjmbr-53-6-e9031-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/6dc85d853fde/1414-431X-bjmbr-53-6-e9031-gf004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/3d521313e0b0/1414-431X-bjmbr-53-6-e9031-gf001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/00b3c4506d16/1414-431X-bjmbr-53-6-e9031-gf002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/70d8136835a1/1414-431X-bjmbr-53-6-e9031-gf003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce59/7228546/6dc85d853fde/1414-431X-bjmbr-53-6-e9031-gf004.jpg

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