TY - JOUR
T1 - The “rectosigmoid brake”
T2 - Review of an emerging neuromodulation target for colorectal functional disorders
AU - Lin, Anthony Y.
AU - Dinning, Phil G.
AU - Milne, Tony
AU - Bissett, Ian P.
AU - O'Grady, Gregory
PY - 2017/7
Y1 - 2017/7
N2 - The regulation of gastrointestinal motility encompasses several overlapping mechanisms including highly regulated and coordinated neurohormonal circuits. Various feedback mechanisms or “brakes” have been proposed. While duodenal, jejunal, and ileal brakes are well described, a putative distal colonic brake is less well defined. Despite the high prevalence of colonic motility disorders, there is little knowledge of colonic motility owing to difficulties with organ access and technical difficulties in recording detailed motor patterns along its entire length. The motility of the colon is not under voluntary control. A wide range of motor patterns is seen, with long intervals of intestinal quiescence between them. In addition, the use of traditional manometric catheters to record contractile activity of the colon has been limited by the low number of widely spaced sensors, which has resulted in the misinterpretation of colonic motor patterns. The recent advent of high-resolution (HR) manometry is revolutionising the understanding of gastrointestinal motor patterns. It has now been observed that the most common motor patterns in the colon are repetitive two to six cycles per minute (cpm) propagating events in the distal colon. These motor patterns are prominent soon after a meal, originate most frequently in the rectosigmoid region, and travel in the retrograde direction. The distal prominence and the origin of these motor patterns raise the possibility of them serving as a braking mechanism, or the “rectosigmoid brake,” to limit rectal filling. This review aims to describe what is known about the “rectosigmoid brake,” including its physiological and clinical significance and potential therapeutic applications.
AB - The regulation of gastrointestinal motility encompasses several overlapping mechanisms including highly regulated and coordinated neurohormonal circuits. Various feedback mechanisms or “brakes” have been proposed. While duodenal, jejunal, and ileal brakes are well described, a putative distal colonic brake is less well defined. Despite the high prevalence of colonic motility disorders, there is little knowledge of colonic motility owing to difficulties with organ access and technical difficulties in recording detailed motor patterns along its entire length. The motility of the colon is not under voluntary control. A wide range of motor patterns is seen, with long intervals of intestinal quiescence between them. In addition, the use of traditional manometric catheters to record contractile activity of the colon has been limited by the low number of widely spaced sensors, which has resulted in the misinterpretation of colonic motor patterns. The recent advent of high-resolution (HR) manometry is revolutionising the understanding of gastrointestinal motor patterns. It has now been observed that the most common motor patterns in the colon are repetitive two to six cycles per minute (cpm) propagating events in the distal colon. These motor patterns are prominent soon after a meal, originate most frequently in the rectosigmoid region, and travel in the retrograde direction. The distal prominence and the origin of these motor patterns raise the possibility of them serving as a braking mechanism, or the “rectosigmoid brake,” to limit rectal filling. This review aims to describe what is known about the “rectosigmoid brake,” including its physiological and clinical significance and potential therapeutic applications.
KW - colon
KW - gastrointestinal motility
KW - gastrointestinal tract
KW - high-resolution manometry
KW - rectosigmoid brake
UR - http://www.scopus.com/inward/record.url?scp=85021329803&partnerID=8YFLogxK
U2 - 10.1111/1440-1681.12760
DO - 10.1111/1440-1681.12760
M3 - Review article
C2 - 28419527
AN - SCOPUS:85021329803
SN - 0305-1870
VL - 44
SP - 719
EP - 728
JO - Clinical and Experimental Pharmacology and Physiology
JF - Clinical and Experimental Pharmacology and Physiology
IS - 7
ER -