TY - JOUR
T1 - Aging of enteric neuromuscular systems in gastrointestinal tract
AU - Nguyen, Vy Truong Thuy
AU - Taheri, Negar
AU - Chandra, Abhishek
AU - Hayashi, Yujiro
N1 - Funding Information:
This work was supported in part by the National Institutes of Health grants R01 DK121766 (Y.H.), Mayo Clinic Center for Biomedical Discovery Pilot Award (Y.H.), and American Gastroenterology Association-Allergan Foundation Pilot Research Award in Gastroparesis (Y.H.), P30 DK084567 (Mayo Clinic Center for Cell Signaling in Gastroenterology). The funding agencies had no role in the study analysis or writing of the manuscript. Its contents are solely the responsibility of the authors. The authors thank Dr. Simon J. Gibbons (Mayo Clinic) for critical suggestions and discussions.
Funding Information:
This work was supported in part by the National Institutes of Health grants R01 DK121766 (Y.H.), Mayo Clinic Center for Biomedical Discovery Pilot Award (Y.H.), and American Gastroenterology Association‐Allergan Foundation Pilot Research Award in Gastroparesis (Y.H.), P30 DK084567 (Mayo Clinic Center for Cell Signaling in Gastroenterology). The funding agencies had no role in the study analysis or writing of the manuscript. Its contents are solely the responsibility of the authors.
Publisher Copyright:
© 2022 John Wiley & Sons Ltd.
PY - 2022/6
Y1 - 2022/6
N2 - Background: Aging is a complex biological process and associated with a progressive decline in functions of most organs including the gastrointestinal (GI) tract. Age-related GI motor disorders/dysfunctions include esophageal reflux, dysphagia, constipation, fecal incontinence, reduced compliance, and accommodation. Although the incidence and severity of these diseases and conditions increase with age, they are often underestimated due in part to nonspecific and variable symptoms and lack of sufficient medical attention. They negatively affect quality of life and predispose the elderly to other diseases, sarcopenia, and frailty. The mechanisms underlying aging-associated GI dysfunctions remain unclear, and there is limited data examining the effect of aging on GI motor functions. Many studies on aging-associated changes to cells within the tunica muscularis including enteric neurons, smooth muscles, and interstitial cells have proposed that cell loss and/or molecular changes may be involved in the pathogenesis of age-related GI motor disorders/dysfunctions. There is also evidence that the aging contributes to phenotypic changes in innate immune cells, which are physically and functionally linked to other cells in the tunica muscularis and can alter GI (patho) physiology. However, various patterns of changes have been reported, some of which are contradictory, indicating a need for additional work in this area. Purpose: Although GI infection due to intestinal bacterial overgrowth, bleeding, and cancers are also important and common problems in the elderly patients, this mini-review focuses on data obtained from enteric neuromuscular aging research with the goal of better understanding the cellular and molecular mechanisms of enteric neuromuscular aging to enhance future therapy.
AB - Background: Aging is a complex biological process and associated with a progressive decline in functions of most organs including the gastrointestinal (GI) tract. Age-related GI motor disorders/dysfunctions include esophageal reflux, dysphagia, constipation, fecal incontinence, reduced compliance, and accommodation. Although the incidence and severity of these diseases and conditions increase with age, they are often underestimated due in part to nonspecific and variable symptoms and lack of sufficient medical attention. They negatively affect quality of life and predispose the elderly to other diseases, sarcopenia, and frailty. The mechanisms underlying aging-associated GI dysfunctions remain unclear, and there is limited data examining the effect of aging on GI motor functions. Many studies on aging-associated changes to cells within the tunica muscularis including enteric neurons, smooth muscles, and interstitial cells have proposed that cell loss and/or molecular changes may be involved in the pathogenesis of age-related GI motor disorders/dysfunctions. There is also evidence that the aging contributes to phenotypic changes in innate immune cells, which are physically and functionally linked to other cells in the tunica muscularis and can alter GI (patho) physiology. However, various patterns of changes have been reported, some of which are contradictory, indicating a need for additional work in this area. Purpose: Although GI infection due to intestinal bacterial overgrowth, bleeding, and cancers are also important and common problems in the elderly patients, this mini-review focuses on data obtained from enteric neuromuscular aging research with the goal of better understanding the cellular and molecular mechanisms of enteric neuromuscular aging to enhance future therapy.
KW - aging
KW - enteric neuron
KW - gastrointestinal motility
KW - interstitial cells of Cajal
KW - muscularis propria macrophage
KW - senescence
UR - http://www.scopus.com/inward/record.url?scp=85126114080&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85126114080&partnerID=8YFLogxK
U2 - 10.1111/nmo.14352
DO - 10.1111/nmo.14352
M3 - Review article
C2 - 35279912
AN - SCOPUS:85126114080
SN - 1350-1925
VL - 34
JO - Neurogastroenterology and Motility
JF - Neurogastroenterology and Motility
IS - 6
M1 - e14352
ER -