Clozapine is a functional antagonist at cardiac human H2-histamine receptors

Clozapine is an atypical antipsychotic (neuroleptic) drug. Clozapine binds to H<sub>2</sub>-histamine receptors in vitro. We wanted to test the hypothesis that clozapine might be a functional antagonist at human cardiac H<sub>2</sub>-histamine receptors. To that end, we studied isolated electrically stimulated left atrial preparations and spontaneously beating right atrial preparations from transgenic mice with cardiomyocyte-specific overexpression of the human H<sub>2</sub>-histamine receptor (H<sub>2</sub>-TG). For comparison, we used wild-type littermate mice (WT). Finally, we measured isometric force of contraction in isolated electrically stimulated muscle strips from the human right atrium (HAP) obtained from patients during bypass surgery. After pre-stimulation with histamine, clozapine (up to 10 µM) concentration and time dependently decreased beating rate in right atrial preparations from H<sub>2</sub>-TG. Clozapine concentration dependently 1, 3, and 10 µM decreased histamine-stimulated force of contraction in HAP. Clozapine (10 µM) decreased also the isoprenaline-stimulated force of contraction in HAP. In summary, clozapine can antagonize the function of H<sub>2</sub>-histamine and β-receptors in the human heart.

Authors

Institutions

Publication Details

Journal
Naunyn-Schmiedeberg s Archives of Pharmacology
Published
2024-12-11
DOI
https://doi.org/10.1007/s00210-024-03683-7
Citations
1
Primary Topic
Receptor Mechanisms and Signaling
Type
article
Field-Weighted Citation Impact
0.23
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clozapine is a functional antagonist at cardiac human H2-histamine receptors

Uwe Kirchhefer, Ulrich Gergs, Britt Hofmann, Joachim Neumann et al.
1 citations
Naunyn-Schmiedeberg s Archives of Pharmacology
Receptor Mechanisms and Signaling
0.23
article

Clozapine is a functional antagonist at cardiac human H2-histamine receptors

Uwe Kirchhefer, Ulrich Gergs, Britt Hofmann, Joachim Neumann, Jonas Manfred Albert Schlicht, Undine Ahlrep
article en
1 citations

Abstract

Clozapine is an atypical antipsychotic (neuroleptic) drug. Clozapine binds to H<sub>2</sub>-histamine receptors in vitro. We wanted to test the hypothesis that clozapine might be a functional antagonist at human cardiac H<sub>2</sub>-histamine receptors. To that end, we studied isolated electrically stimulated left atrial preparations and spontaneously beating right atrial preparations from transgenic mice with cardiomyocyte-specific overexpression of the human H<sub>2</sub>-histamine receptor (H<sub>2</sub>-TG). For comparison, we used wild-type littermate mice (WT). Finally, we measured isometric force of contraction in isolated electrically stimulated muscle strips from the human right atrium (HAP) obtained from patients during bypass surgery. After pre-stimulation with histamine, clozapine (up to 10 µM) concentration and time dependently decreased beating rate in right atrial preparations from H<sub>2</sub>-TG. Clozapine concentration dependently 1, 3, and 10 µM decreased histamine-stimulated force of contraction in HAP. Clozapine (10 µM) decreased also the isoprenaline-stimulated force of contraction in HAP. In summary, clozapine can antagonize the function of H<sub>2</sub>-histamine and β-receptors in the human heart.

Naunyn-Schmiedeberg s Archives of PharmacologyVol. 398(6)
University of Münster (DE), University Hospital in Halle (DE), Martin Luther University Halle-Wittenberg (DE)
Good health and well-being
Openalex Percentile: Top 40%
Receptor Mechanisms and Signaling
0.23
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.