Aging and gastrointestinal smooth muscle
2004; Elsevier BV; Volume: 125; Issue: 12 Linguagem: Inglês
10.1016/j.mad.2004.05.010
ISSN1872-6216
AutoresKhalil N. Bitar, Suresh B. Patil,
Tópico(s)Gastrointestinal motility and disorders
ResumoThe present review is an attempt to put into perspective the available information on the putative changes in cellular mechanisms of the contractile properties of the aging gastrointestinal (GI) smooth muscle. Information on smooth muscle of the GI tract is scanty. Smooth muscle cells from old rats (32 months old) exhibit limited cell length distribution and diminished contractility. The observed reduced contractile response may be due to the effect of aging on signal transduction pathways, especially an inhibition of the tyrosine kinase–Src kinase pathway, a reduced activation of the PKCα pathway, a reduced association of contractile proteins (HSP27-tropomyosin, HSP27-actin, and actin–myosin). Levels of HSP27-phosphorylation are also reduced compared to adult rats. Regulation of GI motility is a complex mechanism of signal transduction and interaction of signaling and contractile proteins. It is suggested that further studies to elucidate the role of HSP27 in aging smooth muscle of the GI tract are needed.
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