Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 is a protein that in humans is encoded by the HCN1 gene.
Function
Hyperpolarization-activated cation channels of the HCN gene family, such as HCN1, contribute to spontaneous rhythmic activity in both heart and brain.
Tissue distribution
HCN1 channel expression is found in the sinoatrial node, the neocortex, hippocampus, cerebellar cortex, dorsal root ganglion, trigeminal ganglion and brainstem.
Ligands
- Ketamine is an inhibitor of HCN1 in addition to its other targets.
- Propofol also inhibits HCN1.
- Isoflurane and Sevoflurane inhibit HCN1.
Interactions
HCN1 has been shown to interact with HCN2.
Epilepsy
De novo mutations in HCN1 cause epilepsy.
See also
- Cyclic nucleotide-gated ion channel
References
Further reading
External links
- HCN1 protein, human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Overview of all the structural information available in the PDB for UniProt: O60741 (Human Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1) at the PDBe-KB.
- Overview of all the structural information available in the PDB for UniProt: O88704 (Mouse Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1) at the PDBe-KB.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
