The impact of sex hormones on genital wound healing in mice: a comparative study. Issue 6 (December 2019)
- Record Type:
- Journal Article
- Title:
- The impact of sex hormones on genital wound healing in mice: a comparative study. Issue 6 (December 2019)
- Main Title:
- The impact of sex hormones on genital wound healing in mice: a comparative study
- Authors:
- Chua, Michael E.
Rong, Mo
Tuba-ang, Karen
Silangcruz, Jan Michael A.
Tanseco, Patrick P.
Ming, Jessica Megan C.
Kim, Kyoung-Han
Hui, Chi Chung
Farhat, Walid A. - Abstract:
- Summary: Introduction and objective: The effects estrogen and testosterone have on penile wound healing are still uncertain. This study evaluated the effects of these hormones on the wound healing process of penile and non-penile skin in wild-type ( Mus musculus species) 4–5-week-old mice. Methodology: Seventy wild-type Mus musculus species were randomly assigned to four groups control ( n = 17), 1-week post-operative topical estrogen ( n = 18), 1-week pre-operative testosterone ( n = 17), and immediate post-operative testosterone ( n = 18). Incisions were made on the ventrum of the penis and dorsal neck skin. On post-operative day 3, 7, and 14, incision sites were harvested. Evaluation was performed grossly for postsurgical penile edema and histologically for inflammatory cell concentration, presence of fibrinopurulent materials and distribution of collagen-fibroblastic cells. Each treatment group was compared at the three post-operative time points using the Fisher—Freeman--Halton exact test. CD34 and androgen receptor immunohistostaining was performed for between-group differences to assess microvascular density or vasodilatation and androgen receptor upregulation. Results: In this study, the experiment noted significant penile edema on post-operative day 7 in the testosterone groups, whereas less edema in the estrogen group ( P = 0.010; Figure). On histologic evaluation of the penile wounds, a significantly increased inflammatory cell concentration was noted forSummary: Introduction and objective: The effects estrogen and testosterone have on penile wound healing are still uncertain. This study evaluated the effects of these hormones on the wound healing process of penile and non-penile skin in wild-type ( Mus musculus species) 4–5-week-old mice. Methodology: Seventy wild-type Mus musculus species were randomly assigned to four groups control ( n = 17), 1-week post-operative topical estrogen ( n = 18), 1-week pre-operative testosterone ( n = 17), and immediate post-operative testosterone ( n = 18). Incisions were made on the ventrum of the penis and dorsal neck skin. On post-operative day 3, 7, and 14, incision sites were harvested. Evaluation was performed grossly for postsurgical penile edema and histologically for inflammatory cell concentration, presence of fibrinopurulent materials and distribution of collagen-fibroblastic cells. Each treatment group was compared at the three post-operative time points using the Fisher—Freeman--Halton exact test. CD34 and androgen receptor immunohistostaining was performed for between-group differences to assess microvascular density or vasodilatation and androgen receptor upregulation. Results: In this study, the experiment noted significant penile edema on post-operative day 7 in the testosterone groups, whereas less edema in the estrogen group ( P = 0.010; Figure). On histologic evaluation of the penile wounds, a significantly increased inflammatory cell concentration was noted for both pre-operative and post-operative testosterone groups on post-operative day 14 ( P = 0.023). The estrogen group revealed significantly increased fibrinopurulent material on the 3rd and 7th post-operative days ( P = 0.045 and P = 0.005, respectively). No significant between-group differences in the collagen-fibroblastic distribution were noted over the three-time phases. On histologic evaluation of the skin wounds, no significant differences were noted between the groups for inflammatory cell concentration and presence of fibrinopurulent materials. However, compared with the testosterone treatment groups, a significant higher collagen-fibroblast distribution was noted in the estrogen groups on post-operative day 3 and 14 ( P = 0.001 and P = 0.044, respectively). Conclusion: Sex hormones, when given peri-operatively, may affect the wound healing process in mice. Testosterone appears to stimulate a prolonged inflammatory effect on penile wounds. Conversely, estrogen induces a fibrinopurulent congregation early in the penile wound healing process. For general skin healing, estrogen induces earlier collagen and fibroblast distribution, whereas testosterone has a delayed effect. The findings of this study should be further investigated in larger animal model with longer follow-up period. Summary Fig. Fig. 1 … (more)
- Is Part Of:
- Journal of pediatric urology. Volume 15:Issue 6(2019)
- Journal:
- Journal of pediatric urology
- Issue:
- Volume 15:Issue 6(2019)
- Issue Display:
- Volume 15, Issue 6 (2019)
- Year:
- 2019
- Volume:
- 15
- Issue:
- 6
- Issue Sort Value:
- 2019-0015-0006-0000
- Page Start:
- 635
- Page End:
- 641
- Publication Date:
- 2019-12
- Subjects:
- Testosterone -- Estrogen -- Wound healing -- CD34 -- Collagen
animal use protocol (AUP) -- Confidence interval (CI) -- hematoxylin and eosin (H&E) -- Interclass correlation coefficient (ICC)
Pediatric urology -- Periodicals
Urologic Diseases -- Periodicals
Urogenital Diseases -- Periodicals
Urologic Surgical Procedures -- Periodicals
Child
Infant
Urologie pédiatrique -- Périodiques
Appareil urinaire -- Maladies -- Périodiques
Pédiatrie
Urologie
Pediatric urology
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
Electronic journals
Periodicals
Electronic journals
618.926 - Journal URLs:
- http://www.sciencedirect.com/science/journal/14775131 ↗
http://www.sciencedirect.com/science/journal/14775131 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jpurol.2019.09.001 ↗
- Languages:
- English
- ISSNs:
- 1477-5131
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5030.285000
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