Thyrotropin-releasing hormone: an inhibitory regulatory peptide of feline lower esophageal sphincter

1993 ◽  
Vol 264 (3) ◽  
pp. G522-G527 ◽  
Author(s):  
H. P. Parkman ◽  
J. C. Reynolds ◽  
C. P. Ogorek ◽  
M. S. Kreider

The functional role of thyrotropin-releasing hormone (TRH) at the lower esophageal sphincter (LES) was examined in the cat. The specific aims of this study were to determine: 1) the relative distribution of TRH throughout the feline gastrointestinal tract and 2) the effect of TRH on LES basal pressures and its response to exogenously induced contractions. TRH concentrations were determined by radioimmunoassay in tissue extracts from 12 sites. The mean concentration of TRH at the manometrically determined LES was 240 +/- 85 pg/g wet wt tissue, and the maximal concentration was just distal to the LES (659 +/- 189 pg/g wet wt). TRH concentration was higher in the mucosa than the underlying muscle layer of the fundus, antrum, duodenum, and ileum. In physiological studies, TRH given selectively via the left gastric artery had no effect on basal LES or esophageal pressures. TRH (2.8 x 10(-8) mol/kg) decreased the LES response to the D50 of substance P by 47.2% (34.8 +/- 3.1 to 18.4 +/- 2.9 mmHg, P < 0.01). In the presence of tetrodotoxin, TRH gave a similar inhibition of substance P-induced contractions (53.5%). TRH also decreased bombesin-induced contractions by 47.5% (29.6 +/- 6.0 to 15.8 +/- 3.9 mmHg, P < 0.025). TRH, however, had no effect on bethanechol-induced contractions. We conclude that 1) TRH is present throughout the gastrointestinal tract, with highest concentrations in the region distal to the LES; 2) TRH has no effect on basal LES tone; and 3) TRH inhibits the LES response to endogenously released and exogenous substance P but not the LES response to bethanechol.(ABSTRACT TRUNCATED AT 250 WORDS)

Life Sciences ◽  
1979 ◽  
Vol 24 (12) ◽  
pp. 1059-1065 ◽  
Author(s):  
John E. Morley ◽  
Joseph H. Steinbach ◽  
Edward J. Feldman ◽  
Travis E. Solomon

1984 ◽  
Vol 62 (2) ◽  
pp. 248-251 ◽  
Author(s):  
S. B. Backman ◽  
J. L. Henry

When applied by iontophoresis onto single sympathetic preganglionic neurones in the intermediolateral nucleus of spinal segments T1–T3 in the cat, substance P and thyrotropin-releasing hormone (TRH) each had a weak excitatory effect. Two-thirds of the neurones studied were excited by substance P while one-fifth were excited by TRH. The time courses of the responses to substance P and to TRH were similar, and consisted of an increase in the rate of discharge with a latency of approximately 30 s from the onset of application. They were also prolonged (30–320 s) in afterdischarge following termination of application. These results indicate that substance P and TRH exert excitatory effects on single sympathetic preganglionic neurones, and support the possibility that they may be chemical mediators of synaptic transmission in the intermediolateral nucleus.


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