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This Article Full Text Full Text (PDF) All Versions of this Article: 294/5/R1704    most recent 00714.2007v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Wright, C. L. Articles by Boulant, J. A. PubMed PubMed Citation Articles by Wright, C. L. Articles by Boulant, J. A.

SLEEP AND TEMPERATURE REGULATION

Cyclic GMP alters the firing rate and thermosensitivity of hypothalamic neurons

¹Department of Physiology and Cell Biology, Ohio State University, Columbus, Ohio; ²Office of the Director, National Institutes of Health, Bethesda, Maryland; and ³Department of Neuroscience, Ohio State University, Columbus, Ohio

Submitted 4 October 2007 ; accepted in final form 27 February 2008

The rostral hypothalamus, especially the preoptic-anterior hypothalamus (POAH), contains temperature-sensitive and -insensitive neurons that form synaptic networks to control thermoregulatory responses. Previous studies suggest that the cyclic nucleotide cGMP is an important mediator in this neuronal network, since hypothalamic microinjections of cGMP analogs produce hypothermia in several species. In the present study, immunohistochemisty showed that rostral hypothalamic neurons contain cGMP, guanylate cyclase (necessary for cGMP synthesis), and CNG A2 (an important cyclic nucleotide-gated channel). Extracellular electrophysiological activity was recorded from different types of neurons in rat hypothalamic tissue slices. Each recorded neuron was classified according to its thermosensitivity as well as its firing rate response to 2–100 µM 8-bromo-cGMP (a membrane-permeable cGMP analog). cGMP has specific effects on different neurons in the rostral hypothalamus. In the POAH, the cGMP analog decreased the spontaneous firing rate in 45% of temperature-sensitive and -insensitive neurons, an effect that is likely due to cGMP-enhanced hyperpolarizing K⁺ currents. This decreased POAH activity could attenuate thermoregulatory responses and produce hypothermia during exposures to cool or neutral ambient temperatures. Although 8-bromo-cGMP did not affect the thermosensitivity of most POAH neurons, it did increase the warm sensitivity of neurons in other hypothalamic regions located dorsal, lateral, and posterior to the POAH. This increased thermosensitivity may be due to pacemaker currents that are facilitated by cyclic nucleotides. If some of these non-POAH thermosensitive neurons promote heat loss or inhibit heat production, then their increased thermosensitivity could contribute to cGMP-induced decreases in body temperature.

guanosine monophosphate; neuronal activity; soluble guanylate cyclase; cyclic nucleotide-gated channel; immunohistochemistry; electrophysiology