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Fermented Maillard reaction products attenuate stress-induced testicular dysfunction in mice

Authors
Joung, Jae YeonLee, Ji SunOh, Nam SuKim, Sae Hun
Issue Date
Feb-2021
Publisher
ELSEVIER SCIENCE INC
Keywords
chronic stress; testicular dysfunction; spermatogenesis; Lactobacillus rhamnosus 4B15; Maillard reaction product
Citation
JOURNAL OF DAIRY SCIENCE, v.104, no.2, pp.1384 - 1393
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF DAIRY SCIENCE
Volume
104
Number
2
Start Page
1384
End Page
1393
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/50037
DOI
10.3168/jds.2020-18996
ISSN
0022-0302
Abstract
Chronic stress can cause psychological diseases and affect male fertility and the reproductive system. Maillard reaction of milk proteins improves their functional and nutritional properties through modification of proteins. Previously, we determined that Maillard reaction product (MRP) from milk casein and MRP fermented (FMRP) with Lactobacillus rhamnosus 4B15 (4B15) had anti-anxiolytic effects in mice under chronic stress. Therefore, we aimed to investigate the effects of MRP and FMRP on chronic stress-induced testicular dysfunction in mice through quantitative real-time PCR (qRT-PCR) and in situ hybridization analysis. Mice were pretreated with MRP and FMRP for 10 wk; simultaneously, from the third week of the experimental period, they were exposed to unpredictable chronic mild stress (UCMS) for 7 wk. The expression levels of the luteinizing hormone subunit [3 (Lhb) and follicle-stimulating hormone subunit 13 (Fshb) were remarkably reduced after exposure to UCMS. However, treatment with MRP and FMRP inhibited the UCMS-induced reduction, with FMRP showing especially significant inhibition. Moreover, the expression of steroidogenesis-related genes [luteinizing hormone receptor (Lhr), follicle-stimulating hormone (Fshr), 3-3 hydroxysteroid dehydrogenase 2 (HsdSb2), and steroidogenic acute regulatory protein (StAR)] were significantly reduced in response to UCMS. In contrast, the transcript levels of these genes were highest in the MRP-treated mice. Mice pretreated with FMRP also exhibited higher levels of gene expression compared with the nonstressed mice. Moreover, UCMS significantly downregulated the expression of genes associated with testicular function [i.e., a disintegrin and metallopeptidase domain 5 (Adam5), Adam29, bone morphogenetic protein 2 (Bmp2), tektin 3 (Tekt3), and sperm adhesion molecule 1 (Spam1]. However, the administration of MRP and FMRP prevented the UCMS-induced reduction in the expressions of above genes. The localization of Lhr, Srd5a2, Adam29, and Spam1 was confirmed by in situ hybridization analysis and the results were consistent with those of qRT-PCR. Consequently, these results indicated that MRP and FMRP, manufactured by the heat treatment of milk casein and fermentation with probiotic 4B15, have the potential to prevent chronic stress-induced testicular dysfunction.
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