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Histamine release induced by neurotensin from rat peritoneal mast cells.
Eur J Pharmacol. 1981 Dec 03; 76(2-3):129-36.EJ

Abstract

Neurotensin induced the release of histamine from both purified and non-purified rat peritoneal mast cells by a non-cytotoxic mechanism. It was effective at a concentration as low as 10(-8) M. The dose-response curve for the neurotensin effect was triphasic: and initial gentle rise, a plateau (2.5 X 10(-7) -2.5 X 10(-6) M) and a second rise. Disodium cromoglycate markedly, but benzalkonium chloride only slightly, inhibited the neurotensin-induced release. The effect of neurotensin was markedly different from that of substance P, bradykinin and compound 48/80 with respect to both the dose-response curve and the sensitivity to benzalkonium chloride. These inducers of histamine release showed somewhat different effects with changes in pH and temperature. Their actions did not require extracellular Ca2+. The results indicate that neurotensin is a potent histamine releaser acting directly on mast cells. Its mode of action may be different from those of the other substances tested.

Authors

No affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

6174350

Citation

Kurose, M, and K Saeki. "Histamine Release Induced By Neurotensin From Rat Peritoneal Mast Cells." European Journal of Pharmacology, vol. 76, no. 2-3, 1981, pp. 129-36.
Kurose M, Saeki K. Histamine release induced by neurotensin from rat peritoneal mast cells. Eur J Pharmacol. 1981;76(2-3):129-36.
Kurose, M., & Saeki, K. (1981). Histamine release induced by neurotensin from rat peritoneal mast cells. European Journal of Pharmacology, 76(2-3), 129-36.
Kurose M, Saeki K. Histamine Release Induced By Neurotensin From Rat Peritoneal Mast Cells. Eur J Pharmacol. 1981 Dec 3;76(2-3):129-36. PubMed PMID: 6174350.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Histamine release induced by neurotensin from rat peritoneal mast cells. AU - Kurose,M, AU - Saeki,K, PY - 1981/12/3/pubmed PY - 1981/12/3/medline PY - 1981/12/3/entrez SP - 129 EP - 36 JF - European journal of pharmacology JO - Eur J Pharmacol VL - 76 IS - 2-3 N2 - Neurotensin induced the release of histamine from both purified and non-purified rat peritoneal mast cells by a non-cytotoxic mechanism. It was effective at a concentration as low as 10(-8) M. The dose-response curve for the neurotensin effect was triphasic: and initial gentle rise, a plateau (2.5 X 10(-7) -2.5 X 10(-6) M) and a second rise. Disodium cromoglycate markedly, but benzalkonium chloride only slightly, inhibited the neurotensin-induced release. The effect of neurotensin was markedly different from that of substance P, bradykinin and compound 48/80 with respect to both the dose-response curve and the sensitivity to benzalkonium chloride. These inducers of histamine release showed somewhat different effects with changes in pH and temperature. Their actions did not require extracellular Ca2+. The results indicate that neurotensin is a potent histamine releaser acting directly on mast cells. Its mode of action may be different from those of the other substances tested. SN - 0014-2999 UR - https://www.unboundmedicine.com/medline/citation/6174350/Histamine_release_induced_by_neurotensin_from_rat_peritoneal_mast_cells_ L2 - https://linkinghub.elsevier.com/retrieve/pii/0014-2999(81)90494-5 DB - PRIME DP - Unbound Medicine ER -