Effects of high-fat diet on the testicular function of sirtuin 1 (SIRT1) knockout male mice

서지정보

ㆍ발행기관 : 충북대학교 동물의학연구소 ㆍ수록지정보 : Journal of Biomedical and Translational Research / 23권 / 4호
ㆍ저자명 : Malavige Romesha Chandanee, Sang-Myeong Lee, Young-Joo Yi

목차

Abstract
INTRODUCTION
MATERIALS AND METHODS
Intake of normal and high-fat diet (HFD) in mice
Examination of organs and epididymal spermatozoa
Hepatotoxicity assessment
Enzyme-linked immunosorbent assay
Serum testosterone assay
Real-time PCR analysis
Histological assessment
Statistical analysis
RESULTS
Changes in organ weight and morphology due to high-fat diet (HFD)
Increased hepatotoxicity and testosterone levels in sirtuin 1 (SIRT1)-high-fat diet(HFD) mice
Cytokine levels and oxidative stress on sirtuin 1 (SIRT1)-high-fat diet (HFD) mice
RNA expressions of proteins in the blood-testis barrier (BTB), histological analysisof testicular tissue and quality of epididymal spermatozoa
DISCUSSION
REFERENCES

영어 초록

Sirtuin 1 (SIRT1), the most conserved nicotinamide adenine dinucleotide-dependent protein deacetylase, is involved in the regulation of energy metabolism, genomic stability, and development. SIRT1 knockout (SIRT1) mice exhibit decreased energy expenditure and hypersensitivity to a high-fat diet (HFD). SIRT1 deficiency in the testis has also been shown to cause male infertility in animal models. Therefore, the present study was conducted to examine the alteration of the testicular function of SIRT1 mice on HFD. Six-week-old mice were fed ad libitum as wild type (WT) and SIRT1 male mice with either a control diet or with HFD for 32 weeks and then were sacrificed. The levels of biomarkers for hepatotoxicity, sex hormones, and cytokines were analyzed in the serum and blood-testis barrier, and the sperm morphology was examined in the testis and epididymal spermatozoa. Interestingly, an enlargement of seminal vesicles was observed in the SIRT1 mice fed with HFD. A significantly higher level of hepatotoxicity was also seen in these mice. The concentration of serum testosterone increased in HFD-fed SIRT1 mice compared to the controls. The levels of interleukin-1β and TNF-α increased in both HFD-fed WT and SIRT1 mice. In RT-PCR, the m RNA expression of tight junction protein 2 and claudin 3 significantly decreased in HFD-fed SIRT1 compared to those of the controls. Degenerative spermatocytes and spermatids were detected in the HFD-fed SIRT1 mice testicular section. Sperm motility decreased in WT and SIRT1 with HFD feeding, and sperm concentration decreased significantly in WT-HFD and SIRT1 mice with or without HFD feeding. Taken together, HFD can alter energy and steroid metabolism in SIRT1-deficient mice, which can lead to imbalances in motility and production of sperm and testosterone that can result in male reproductive disorders.

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