Expression of cyclooxygenase-2 in the canine lower urinary tract with regard to the effects of gonadal status and gender

• Published in: Theriogenology 2009-05, Vol.71 (8), p.1276-1288
• Main Authors: Ponglowhapan, S., Church, D.B., Khalid, M.
• Format: Article
• Language: English
• Subjects: Animals; bladder; castration; Castration - veterinary; COX-2; Cyclooxygenase 2 - genetics; Cyclooxygenase 2 - metabolism; Dog; dogs; Dogs - genetics; Dogs - metabolism; Female; gender differences; Gene Expression; gonadectomy; Gonads - physiology; immunohistochemistry; Lower urinary tract; Male; messenger RNA; prostaglandin synthase; protein synthesis; RNA, Messenger - metabolism; Sex Characteristics; Spaying; tissue distribution; urethra; Urinary incontinence; urinary tract; Urinary Tract - metabolism
• ISSN: 0093-691X; 1879-3231
• DOI: 10.1016/j.theriogenology.2008.12.021

As pituitary gonadotrophins can induce prostaglandin (PG) synthesis and receptors for LH and FSH are present in the canine lower urinary tract (LUT), the objectives of this study were to (i) investigate the expression of COX-2, a key rate-limiting enzyme in PG production, in the canine LUT and (ii) determine if COX-2 expression differs between gender, gonadal status (intact and gonadectomised) and LUT regions. Four regions (body and neck of the bladder as well as proximal and distal urethra) of the LUT were obtained from 20 clinically healthy dogs (5 intact males, 5 intact anoestrous females, 4 castrated males, 6 spayed females). In situ hybridization and immunohistochemistry were performed to determine the presence of COX-2 mRNA and protein, respectively. The mRNA and protein expression was semi-quantitatively assessed. The scoring system combined both the distribution and intensity of positive staining and was carried out separately on the three tissue layers (epithelium, sub-epithelial stroma and muscle) for each of four regions of the LUT. In comparison to intact dogs, lower expression ( P < 0.001) of COX-2 and its mRNA in gonadectomised males and females was observed in all tissue layers of each region of the LUT except in the distal urethra where there was no difference in mRNA expression between gonadal statuses. Regardless of region and tissue layer, intact females expressed more ( P < 0.05) COX-2 and its mRNA than intact males. However, in gonadectomised dogs, mRNA expression of COX-2 did not differ between genders; males had higher ( P < 0.001) protein level of COX-2 compared to females. In conclusion, both COX-2 and its mRNA were expressed in the canine LUT and COX-2-regulated PG synthesis in the canine LUT may differ between gonadal statuses and genders. The lower expression of COX-2 in gonadectomised dogs may impair normal function of the LUT and probably implicated in the development of neutering-induced urinary incontinence in the dog.