Abstract |
Propyl-methylenedioxyindene ( pr-MDI; 30 mg/kg, i.p.), an intracellular calcium antagonist, significantly reduced the number and size of erosions per stomach induced by cold-restraint stress by 69% and 86%, respectively. Our previous findings indicate that the antiulcer activity of pr-MDI is highly correlated with its inhibitory effect on gastric motor activity. Since central TRH is suggested as the brain mediator responsible for cold-restraint stress gastric ulcers in rats, the inhibitory action of pr-MDI was evaluated in the TRH-induced gastric lesion model. Pr-MDI (30 mg/kg) did not reduce the gastric erosions induced by intracisternal administration of 100ng RX77368, a stable thyrotropin-releasing hormone (TRH) analogue, even though it abolished the RX77368-induced stimulation of gastric emptying, gastric acidity, and acid output. Since pr-MDI (30 mg/kg, i.p.) significantly inhibited the stimulation of gastric motility by both cold-restraint stress and TRH, but only cold-restraint stress-induced gastric erosions were effectively reduced by the drug, the present findings suggest a possible dissociation between the ulcerogenic mechanisms of cold-restraint stress and intracisternal administration of TRH.
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Authors | W S Wong, R G Rahwan, R L Stephens Jr |
Journal | Life sciences
(Life Sci)
Vol. 47
Issue 16
Pg. 1483-9
( 1990)
ISSN: 0024-3205 [Print] Netherlands |
PMID | 2123509
(Publication Type: Journal Article)
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Chemical References |
- Anti-Ulcer Agents
- Calcium Channel Blockers
- Indenes
- Thyrotropin-Releasing Hormone
- L-pyroglutamyl-L-histidyl-3,3-dimethylprolinamide
- propylmethylenedioxyindene
- Pyrrolidonecarboxylic Acid
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Topics |
- Animals
- Anti-Ulcer Agents
(therapeutic use)
- Calcium Channel Blockers
(therapeutic use)
- Cold Temperature
- Gastric Acid
(metabolism)
- Gastric Emptying
(drug effects)
- Gastric Juice
(drug effects)
- Indenes
(therapeutic use)
- Male
- Pyrrolidonecarboxylic Acid
(analogs & derivatives)
- Rats
- Rats, Inbred Strains
- Restraint, Physical
- Stomach Ulcer
(chemically induced, drug therapy, etiology)
- Stress, Psychological
- Thyrotropin-Releasing Hormone
(analogs & derivatives, pharmacology)
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