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Cited by 230

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Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine.

Open access
Tran, V T, Chang, R S, Snyder, S H·1978·Proceedings of the National Academy of Sciences

Abstract

The antihistamine [3H]mepyramine binds to H1 histamine receptors in mammalian brain membranes. Potencies of H1 antihistamines at the binding sites correlate with their pharmacological antihistamine effects in the guinea pig ileum. Specific [3H]mepyramine binding is saturable with a dissociation constant of about 4 nM in both equilibrium and kinetic experiments and a density of 10 pmol per gram of whole kinetic experiments and a density of 10 pmol per gram of whole brain. Some tricyclic antidepressants are potent inhibitors of specific [3H]mepyramine binding. Regional variations of [3H]mepyramine binding do not correlate with variations in endogeneous histamine and histidine decarboxylase activity.

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Metadata

Authors
Tran, V. T., Chang, R. S., & Snyder, S. H.
Venue
Proceedings of the National Academy of Sciences
Published
1978-12
Volume
75
Issue
12
Pages
6290-6294
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2022412068
Cited by
230
References
0
FWCI
6.03
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine. https://app.cochat.ai/papers/10.1073/pnas.75.12.6290
The paper
Tran, V. T., Chang, R. S., & Snyder, S. H. (1978). Histamine H1 receptors identified in mammalian brain membranes with [3H]mepyramine. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.75.12.6290

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.