Literature DB >> 15137926

Dietary repletion can replenish reduced T cell subset numbers and lymphoid organ weight in zinc-deficient and energy-restricted rats.

Heather J Hosea1, Edward S Rector, Carla G Taylor.   

Abstract

The objective of the present study was to investigate the time course for recovery of lymphoid tissue and T cell subset numbers when Zn-deficient (ZD) or energy-restricted (ER) rats were repleted with control diet; in a second experiment, the link between the stress axis and lymphoid organs was explored. During the deficiency phase, rats were fed a ZD (<1 mg Zn/kg) or control diet (30 mg Zn/kg, nutritionally complete) either as pair-fed controls (ER) or ad libitum-fed controls (CTL) for 3 weeks. During the repletion phase, all rats were fed control diet ad libitum for 3, 7 or 23 d. After the deficiency phase, ZD and ER had lower T cell subset numbers in the thymus compared with CTL, and ZD had reduced T cell subset numbers in the spleen compared with both ER and CTL. T cell subset numbers and lymphoid organ weights recovered from dietary Zn deficiency and energy restriction by 7 d of repletion (except 23 d for thymus weight in ZD), while body weight required more than 23 d for recovery. At the end of the deficiency phase, ZD and ER had higher circulating corticosterone concentrations compared with CTL; plasma TNFalpha was not detectable and there were no differences in plasma haptoglobin, an acute-phase protein. In conclusion, Zn deficiency and energy restriction elevated circulating corticosterone and reduced T cell subset numbers in the thymus and spleen of growing rats. Repletion with a nutritionally complete diet allowed recovery of T cell subset numbers and lymphoid organ weight.

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Year:  2004        PMID: 15137926     DOI: 10.1079/BJN20041104

Source DB:  PubMed          Journal:  Br J Nutr        ISSN: 0007-1145            Impact factor:   3.718


  5 in total

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Review 2.  Dietary zinc deficiency in rodents: effects on T-cell development, maturation and phenotypes.

Authors:  Heather J Blewett; Carla G Taylor
Journal:  Nutrients       Date:  2012-06-06       Impact factor: 5.717

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Journal:  Sci Rep       Date:  2017-11-09       Impact factor: 4.379

5.  Umbilical cord mesenchymal stem cells protect thymus structure and function in aged C57 mice by downregulating aging-related genes and upregulating autophagy- and anti-oxidative stress-related genes.

Authors:  Xing-Hua Pan; Qing-Keng Lin; Xiang Yao; Zi-An Li; Xue-Min Cai; Rong-Qing Pang; Guang-Ping Ruan
Journal:  Aging (Albany NY)       Date:  2020-09-14       Impact factor: 5.682

  5 in total

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