Key result
Vasoactive intestinal peptide caused greater relaxation of smooth muscle cells in the human antrum (ED50 0.53 nmol/L) compared to the fundus (ED50 3.4 nmol/L) due to distinct myogenic properties.
Population
Human stomach smooth muscle cells (SMC) and strips of the fundus and antrum
Design
Preclinical
Authors
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Regional VIP responsiveness in human stomach warrants targeted motility studies; leaves open clinical translation from isolated cells.
Regional differences in VIP action on the human stomach are related to distinct myogenic properties of smooth muscle cells in the antrum and fundus.
Severi et al. (2006) studied this question. Vasoactive intestinal peptide (VIP) was evaluated on Relaxation of smooth muscle cells and strips. Vasoactive intestinal peptide caused greater relaxation of smooth muscle cells in the human antrum (ED50 0.53 nmol/L) compared to the fundus (ED50 3.4 nmol/L) due to distinct myogenic properties.
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