Impact of acute undernutrition on growth, ileal morphology and nutrient transport in a murine model.
Impact of acute undernutrition on growth, ileal morphology and nutrient transport in a murine model.
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DOI:
10.1590/1414-431x20165340
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发表时间:
2016-10-10
期刊:
影响因子:
--
通讯作者:
Lima AA
中科院分区:
文献类型:
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作者:
Sampaio IC;Medeiros PH;Rodrigues FA;Cavalcante PA;Ribeiro SA;Oliveira JS;Prata MM;Costa DV;Fonseca SG;Guedes MM;Soares AM;Brito GA;Havt A;Moore SR;Lima AA
Undernutrition represents a major public health challenge for middle- and low-income countries. This study aimed to evaluate whether a multideficient Northeast Brazil regional basic diet (RBD) induces acute morphological and functional changes in the ileum of mice. Swiss mice (∼25 g) were allocated into two groups: i) control mice were fed a standard diet and II) undernourished mice were fed the RBD. After 7 days, mice were killed and the ileum collected for evaluation of electrophysiological parameters (Ussing chambers), transcription (RT-qPCR) and protein expression (western blotting) of intestinal transporters and tight junctions. Body weight gain was significantly decreased in the undernourished group, which also showed decreased crypt depth but no alterations in villus height. Electrophysiology measurements showed a reduced basal short circuit current (I sc) in the undernourished group, with no differences in transepithelial resistance. Specific substrate-evoked I sc related to affinity and efficacy (glutamine and alanyl-glutamine) were not different between groups, except for the maximum I sc (efficacy) induced by glucose. Transcription of Sglt1 and Pept1 was significantly higher in the undernourished group, while SN-2 transcription was decreased. No changes were found in transcription of CAT-1 and CFTR, while claudin-2 and occludin transcriptions were significantly increased in the undernourished group. Despite mRNA changes, SGLT-1, PEPT-1, claudin-2 and occludin protein expression showed no difference between groups. These results demonstrate early effects of the RBD on mice, which include reduced body weight and crypt depth in the absence of significant alterations to villus morphology, intestinal transporters and tight junction expression.