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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Toll-like receptor 9 regulates metabolic profile and contributes to obesity-induced benign prostatic hyperplasia in mice

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Author(s):
Calmasini, Fabiano B. [1, 2] ; McCarthy, Cameron G. [1, 3] ; Wenceslau, Camilla F. [1, 3] ; Priviero, Fernanda B. M. [1] ; Antunes, Edson [2] ; Webb, R. Clinton [1]
Total Authors: 6
Affiliation:
[1] Augusta Univ, Dept Physiol, 1120 15th St, Augusta, GA 30912 - USA
[2] Univ Estadual Campinas, Fac Med Sci, Dept Pharmacol, UNICAMP, Campinas - Brazil
[3] Univ Toledo, Coll Med & Life Sci, Dept Physiol & Pharmacol, 2801 W Bancroft St, Toledo, OH 43606 - USA
Total Affiliations: 3
Document type: Journal article
Source: PHARMACOLOGICAL REPORTS; v. 72, n. 1, p. 179-187, FEB 2020.
Web of Science Citations: 0
Abstract

Background Benign prostatic hyperplasia (BPH) is associated with obesity and prostatic inflammation. The present study investigated the participation of toll-like receptor 9 (TLR9) in obesity-induced BPH, focusing on metabolic impairments, damage-associated molecular patterns (DAMP) levels and prostatic oxidative stress generation. Methods C57BL/6 (WT) and TLR9 mutant male mice were fed with regular or high-fat diet for 12 weeks. Metabolic profile, functional protocols, reactive-oxygen species (ROS) generation, prostatic histological analysis and DAMP levels were analyzed. Western blotting for prostatic TLR9 signaling pathway was also performed. Results BPH in WT obese animals was characterized by increased prostate weight, smooth muscle hypercontractility and prostatic epithelial hyperplasia. Higher epididymal fat weight and prostatic ROS generation along with increased fasting glucose, triglyceride and circulating DAMP levels were also observed in WT obese group. Conversely, TLR9 mutant obese animals exhibited lower epididymal fat weight, fasting glucose and triglyceride levels associated with reduced prostate hypercontractility, prostatic ROS and circulating DAMP levels. However, TLR9 mutant obese mice were not protected from obesity-associated prostatic overgrowth and epithelial hyperplasia. Interestingly, TLR9 mutant lean mice exhibited augmented fasting glucose and prostatic ROS levels compared with WT lean mice. Despite increased prostatic expression of TLR9 in WT obese mice, no differences were seen in MyD88 expression between groups. Conclusion Improved obesity-induced BPH-related prostatic smooth muscle hypercontractility in TLR9 obese mice may be associated with amelioration in the metabolic profile, ROS and DAMP generation. Therefore, TLR9 could be a valuable target to improve obesity-associated metabolic disorders and prostate smooth muscle hypercontractility in BPH. (AU)

FAPESP's process: 16/20592-8 - Participation of toll-like receptor 9 (TLR9) in prostate dysfunctions of insulin resistance obese mice
Grantee:Fabiano Beraldi Calmasini
Support Opportunities: Scholarships abroad - Research Internship - Post-doctor