Journal article
Parental High-Fat Diet Promotes Inflammatory and Senescence-Related Changes in Prostate
Oxidative medicine and cellular longevity, Vol.2017, pp.4962950-13
2017
DOI: 10.1155/2017/4962950
PMCID: PMC5316447
PMID: 28261375
Abstract
. Obesity and dietary habits are associated with increased incidences of aging-related prostatic diseases. The present study was aimed to investigate transgenerational effects of chronic high-fat diet (HFD) feeding on inflammation and senescence-related changes in prostate.
. Sprague-Dawley rats were kept on either normal or HFD one. Senescence-associated
-galactosidase (SA
-gal) activity, inflammation, and cellular proliferation were determined in the prostate.
. Increased SA
-gal activity, expression of p53, and cell proliferation marker PCNA were observed in ventral prostate of HFD-fed rats. Immunostaining for p53 and PCNA revealed that the p53 immunopositive cells were primarily in stroma while PCNA immunopositive cells were epithelial cells. An increase in expression of cycloxygenase-2 (COX-2) and phosphorylation of nuclear factor-kappa B (NF-kB) was observed in prostate of weaning pups HFD-fed parents. However, in adult pups, irrespective of dietary habit, a significant increase in the expression of COX-2, PCNA, phosphorylation of NF-kB, infiltration of inflammatory cells, and SA
-gal activity was observed.
Present investigation reports that HFD feeding promotes accumulation of p53 expressing cells, proliferation of epithelial cells, and senescence-related changes in prostate. Further, parental HFD-feeding upholds inflammatory, proliferative, and senescence-related changes in prostate of pups.
Details
- Title: Subtitle
- Parental High-Fat Diet Promotes Inflammatory and Senescence-Related Changes in Prostate
- Creators
- Kulbhushan Tikoo - Laboratory of Epigenetics and Diseases, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, IndiaAjit Vikram - Facility for Risk Assessment and Intervention Studies, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, IndiaShweta Shrivastava - Laboratory of Epigenetics and Diseases, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, IndiaGopabandhu Jena - Facility for Risk Assessment and Intervention Studies, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, IndiaHeta Shah - Laboratory of Epigenetics and Diseases, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, IndiaRicha Chhabra - Laboratory of Epigenetics and Diseases, Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research (NIPER), Mohali, Punjab 160 062, India
- Resource Type
- Journal article
- Publication Details
- Oxidative medicine and cellular longevity, Vol.2017, pp.4962950-13
- DOI
- 10.1155/2017/4962950
- PMID
- 28261375
- PMCID
- PMC5316447
- NLM abbreviation
- Oxid Med Cell Longev
- ISSN
- 1942-0900
- eISSN
- 1942-0994
- Grant note
- DOI: 10.13039/501100001407, name: Department of Biotechnology , Ministry of Science and Technology
- Language
- English
- Date published
- 2017
- Academic Unit
- Cardiovascular Medicine; Fraternal Order of Eagles Diabetes Research Center; Internal Medicine
- Record Identifier
- 9984094517302771
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