Abstract
The hyperpolarization-activated current (I-h) is an inward current activated by hyperpolarization from the resting potential and is an important modulator of action potential firing frequency in many excitable cells. Four hyperpolarization-activated, cyclic nucleotide-modulated subunits, HCN1-4, can form I-h ion channels. In the present study we investigated the function of I-h in primary somatosensory neurons. Neuronal firing in response to current injection was promoted by elevating intracellular cAMP levels and inhibited by blockers of I-h, suggesting that I-h plays a critical role in modulating firing frequency. The properties of I-h in three size classes of sensory neurons were next investigated. In large neurons I-h was fast activating and insensitive to elevations in cAMP, consistent with expression of HCN1. I-h was ablated in most large neurons in HCN1(-/-) mice. In small neurons a slower activating, cAMP-sensitive I-h was observed, as expected for expression of HCN2 and/or HCN4. Consistent with this, I-h in small neurons was unchanged in HCN1(-/-) mice. In a neuropathic pain model HCN1(-/-) mice exhibited substantially less cold allodynia than wild-type littermates, suggesting an important role for HCN1 in neuropathic pain. This work shows that I-h is an important modulator of action potential generation in somatosensory neurons.
Original language | English |
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Pages (from-to) | 5911-5929 |
Number of pages | 19 |
Journal | The Journal of Physiology |
Volume | 586 |
Issue number | 24 |
DOIs | |
Publication status | Published - Dec 2008 |
Keywords
- DORSAL-ROOT GANGLION
- RAT SENSORY NEURONS
- PRIMARY AFFERENT NEURONS
- GATED CATION CHANNELS
- SCIATIC-NERVE INJURY
- PACEMAKER CHANNELS
- NEUROPATHIC PAIN
- PERIPHERAL NEUROPATHY
- NOCICEPTIVE NEURONS
- POTASSIUM CURRENT