Gene expression of histamine H1 receptor in guinea pig primary sensory neurons: a relationship between H1 receptor mRNA-expressing neurons and peptidergic neurons
Abstract
Pharmacological studies have suggested that a subgroup of primary sensory neurons is responsive to histamine via the histamine H1 receptor. We addressed this issue using in situ hybridization histochemistry with a cRNA probe for the guinea pig H1 receptor gene. About 15% of the trigeminal and lumber dorsal root ganglion (DRG) neurons, but none of nodose ganglion neurons, were intensely labeled with this probe. The H1 receptor mRNA-positive neurons were exclusively small in size, and were demonstrated to give rise to unmyelinated fibers by ultrastructural analysis of isolectin B4-labeling. However, the H1 receptor mRNA-expressing DRG neurons were not immunoreactive to substance P (SP) and calcitonin gene-related peptide (CGRP). A marked increase in the number of mRNA-positive DRG neurons were observed 1-5 days after a crush injury of the sciatic nerve (3-4-fold of the control value). These neurons turned mRNA-positive after the nerve crush were also mainly small-sized. The mRNA signals were detected in many peptidergic (SP/CGRP) neurons, in contrast to the normal state. On the other hand, in the neurons which showed intense labeling in the normal condition, the mRNA signals were down-regulated. These results suggest that primary sensory neurons include two kinds of H1 receptor-expressing sensory neurons, one expressing H1 receptor mRNAs in the normal state and the other up-regulating the mRNAs following the peripheral nerve damage.
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Neuronal histamine receptors are upregulated or modulated by nerve injury.
“Histamine is a key mediator released by activated mast cells.It can sensitize nociceptors (14, 15), and neuronal histamine receptors are upregulated or modulated by nerve injury (33,34).”
From Pain, mast cells, and nerves in peritoneal, ovarian, and deep infiltrating endometriosis (2006) · cites this paper as [33]
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References 41 · Cited by 92
- Authors
- Kashiba, H., Fukui, H., Morikawa, Y., & Senba, E.
- Affiliations
- Tokushima University (JP)
- Wakayama Medical University (JP)
- Corresponding author
- Senba, Emiko
- ORCID
- Morikawa, Yoshihiro
- Venue
- Molecular Brain Research
- Publisher
- Elsevier BV
- Published
- 1999-03
- Volume
- 66
- Issue
- 1-2
- Pages
- 24-34
- ISSN
- 0169-328X (ISSN-L)
- OpenAlex
- W1969816505
- Cited by
- 92
- References
- 41
- Citations by year
- 2026: 1 · 2024: 2 · 2022: 1 · 2021: 1 · 2020: 4 · 2018: 2 · 2016: 3 · 2015: 2 · 2014: 2 · 2013: 5 · 2012: 3
- FWCI
- 3.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Molecular Brain Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Ministry of Education, Culture, Sports, Science and Technology
- Topics
- Health Sciences › Medicine › Physiology › Pain Mechanisms and Treatments
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Life Sciences › Immunology and Microbiology › Immunology › Mast cells and histamine
- Keywords
- histamine H1 receptor, primary sensory neurons, dorsal root ganglia, trigeminal ganglion, nodose ganglion, peptidergic neurons, substance P, calcitonin gene-related peptide, nerve crush injury, peripheral nerve injury, mRNA expression, unmyelinated nerve fibers, receptor up-regulation
- MeSH terms
- Animals, Cholera Toxin, Ganglia, Spinal, Guinea Pigs, Horseradish Peroxidase, Male, Microscopy, Electron, Neurons, Afferent, Receptors, Histamine H1, RNA, Messenger, Sciatic Nerve, Substance P, Down-Regulation, Calcitonin Gene-Related Peptide, Up-Regulation, Gene Expression, In Situ Hybridization, Axotomy
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