Age-related external anal sphincter muscle dysfunction and fibrosis: possible role of Wnt/β-catenin signaling pathways

• Published in: American journal of physiology: Gastrointestinal and liver physiology Vol. 313; no. 6; p. G581
• Main Authors: Rajasekaran, M Raj, Kanoo, Sadhana, Fu, Johnny, Nguyen, My-Uyen Lilly, Bhargava, Valmik, Mittal, Ravinder K
• Format: Journal Article
• Language: English
• Published: United States 01-12-2017
• Subjects: Age Factors; Aging - genetics; Aging - metabolism; Aging - pathology; Anal Canal - metabolism; Anal Canal - pathology; Anal Canal - physiopathology; Animals; Atrophy; beta Catenin - genetics; beta Catenin - metabolism; Collagen Type I - genetics; Collagen Type I - metabolism; Female; Fibrosis; Gene Expression Regulation; Muscle Contraction; Muscle, Smooth - metabolism; Muscle, Smooth - pathology; Muscle, Smooth - physiopathology; Rabbits; RNA, Messenger - genetics; RNA, Messenger - metabolism; SKP Cullin F-Box Protein Ligases - genetics; SKP Cullin F-Box Protein Ligases - metabolism; Transforming Growth Factor beta - genetics; Transforming Growth Factor beta - metabolism; Tripartite Motif Proteins - genetics; Tripartite Motif Proteins - metabolism; Wnt Signaling Pathway - genetics; Wnt; fibrosis; aging
• ISSN: 1522-1547
• DOI: 10.1152/ajpgi.00209.2017

Studies show an age-related increase in the prevalence of anal incontinence and sphincter muscle atrophy. The Wnt/β-catenin signaling pathway has been recently recognized as the major molecular pathway involved in age-related skeletal muscle atrophy and fibrosis. The goals of our study were to
) evaluate the impact of normal aging on external anal sphincter (EAS) muscle length-tension (L-T) function and morphology and
) specifically examine the role of Wnt signaling pathways in anal sphincter muscle fibrosis. New Zealand White female rabbits [6 young (6 mo of age) and 6 old (36 mo of age)] were anesthetized, and anal canal pressure was measured to determine the L-T function of EAS. Animals were killed at the end of the study, and the anal canal was harvested and processed for histochemical studies (Masson trichrome stain for muscle/connective tissue) as well as for molecular markers for fibrosis and atrophy [collagen I, β-catenin, transforming growth factor-β (TGF-β), atrogin-1, and muscle-specific RING finger protein-1 (MuRF-1)]. The L-T was significantly impaired in older animals compared with young animals. Anal canal sections stained with trichrome showed a significant decrease in the muscle content (52% in old compared with 70% in young) and an increase in the connective tissue/collagen content in the old animals. An increased protein and mRNA expression of all the fibrosis markers was seen in the older animals. Aging EAS muscle exhibits impairment of function and increase in connective tissue. Upregulation of atrophy and profibrogenic proteins with aging may be the reason for the age-related decrease in anal sphincter muscle thickness and function.
Our studies using a female rabbit model show age-related alterations in the structure and function of the external anal sphincter (EAS) muscle. We used endoluminal ultrasound to measure age-related changes in EAS muscle thickness. We employed Western blot and quantitative PCR to demonstrate age-related changes in the levels of important fibrogenic as well as atrophy markers. Our findings may have significant clinical implications, i.e., use of specific antagonists to prevent age-related EAS muscle dysfunction.