Key result
PAR1 and PAR2 agonists trigger non-neural contraction in human oesophageal muscularis mucosae unlike PAR4 agonists.
PAR1 and PAR2, but not PAR4, mediate non-neural contraction in human oesophageal muscularis mucosae.
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May inform oesophageal motility mechanisms; leaves open PAR1/PAR2 as therapeutic targets pending clinical studies.
Proteinase-activated receptors 1 and 2 mediate contraction of the human gallbladder. In the present study, we investigated effects mediated by proteinase-activated receptors (PARs) in the human oesophagus by measuring contraction of muscularis mucosae strips isolated from the human oesophagus. Both PAR(1) agonists (thrombin, SFLLRN-NH(2) and TFLLR-NH(2)) and PAR(2) agonists (trypsin, 2-furoyl-LIGRLO-NH(2) and SLIGKV-NH(2)) caused concentration-dependent contraction. In contrast, PAR(1) and PAR(2) control peptides did not cause contraction. The existence of PAR(1) and PAR(2) in the human oesophageal muscularis mucosae was confirmed by immunohistochemistry and reverse transcription-polymerase chain reaction. On the other hand, PAR(4) agonists, GYPGKF-NH(2), GYPGQV-NH(2) and AYPGKF-NH(2), did not cause contraction or relaxation in resting or carbachol-contracted muscularis mucosae strips, suggesting that PAR(4) is not involved in human oesophageal motility. The contractile responses to SFLLRN-NH(2) and trypsin in the human oesophagus were insensitive to atropine and tetrodotoxin, indicating that the contractile response was not neurally mediated. Taken together, these results demonstrate that PAR(1) and PAR(2) but not PAR(4) mediate contraction in human oesophageal muscularis mucosae. PAR(1) and PAR(2) may influence human oesophageal motility.
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Chang et al. (2009) studied this question. PAR(1) and PAR(2) agonists vs. Control peptides and PAR(4) agonists was evaluated on Contraction of muscularis mucosae strips. PAR(1) and PAR(2) agonists, but not PAR(4) agonists, caused concentration-dependent, non-neurally mediated contraction in human oesophageal muscularis mucosae strips.
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