Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1990 Jul;96(1):11-21.
doi: 10.1254/fpj.96.1_11.

[Comparative effects of various centrally acting gastric secretagogues including PCPGABA and TRH in the perfused rat stomach preparation]

[Article in Japanese]
Affiliations
Comparative Study

[Comparative effects of various centrally acting gastric secretagogues including PCPGABA and TRH in the perfused rat stomach preparation]

[Article in Japanese]
K Yamasaki et al. Nihon Yakurigaku Zasshi. 1990 Jul.

Abstract

The effects of 2-(p-chlorophenyl)-GABA (PCPGABA), thyrotropin releasing hormone (TRH), insulin and 2-deoxy-D-glucose (2DG) on gastric acid secretion, vagal nerve efferent activity and blood glucose level were examined in anesthetized rats. The latencies of onset of hypersecretion were 10 min for TRH (1 microgram/rat, i.c.), 20 min for PCPGABA (4 mg/kg, s.c.), 60 min for 2DG (200 mg/kg, i.v.) and 90 min for insulin (2 U/kg, i.v.), respectively. The secretagogue actions of PCPGABA and TRH were more potent than those of 2DG and insulin. All these secretagogues caused the efferent activation of the cervical vagal transmission, and the latencies for these vagal activation were shorter than those seen in gastric acid hypersecretion. Atropine and vagotomy completely abolished the secretagogue actions of these stimulants. PCPGABA and TRH were ineffective on the blood glucose level, unlike insulin and 2DG. These results suggest that PCPGABA, TRH, 2DG and insulin stimulate gastric acid secretion via central vagal cholinergic pathways, even though the precise mechanisms for each stimulant seem to be different.

PubMed Disclaimer

Similar articles

Publication types

LinkOut - more resources