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Disruption of GABAergic tone in the dorsomedial hypothalamus attenuates responses in a subset of serotonergic neurons in the dorsal raphe nucleus following lactate–induced panic

¹ Departments of Psychiatry and Biochemistry, Indiana University School of Medicine, 1111 West 100 Street, Suite 313, Indianapolis, IN 46223, USA.
² Henry Wellcome Laboratories for Integrative Neuroscience and Endocrinology, University of Bristol, Bristol, UK.

^* To whom correspondence should be addressed.

	Abstract

Panic patients are vulnerable to induction of panic attacks by sub-threshold interoceptive stimuli such as intravenous (i.v.) sodium lactate infusions. Facilitation of serotonergic signaling with selective serotonin reuptake inhibitors can suppress anxiety and panic–like responses, but the mechanisms involved are not clearly defined. We investigated the effects of i.v. 0.5M sodium lactate or saline, in control and panic–prone rats on c–Fos expression in serotonergic neurons within subdivisions of the midbrain/pontine raphe nuclei. Rats were chronically infused with either the GABA synthesis inhibitor l–allylglycine into the dorsomedial hypo thalamus to make them panic–prone, or the enantiomer d–allylglycine (d–AG) in controls. Lactate increased c–Fos expression in serotonergic neurons located in the ventrolateral part of the dorsal raphe nucleus (DRVL) and ventrolateral periaqueductal gray (VLPAG) of control, but not panic–prone, rats. The distribution of lactate–sensitive serotonergic neurons in d–AG–treated rats is virtually identical to previously defined pre–sympathomotor serotonergic neurons with multisynaptic projections to peripheral organs mediating 'fight–or–flight'–related autonomic and motor responses. We hypothesized that serotonergic neurons within the DRVL/VLPAG region represent a 'sympathomotor control system' that normally limits autonomic/behavioral responses to innocuous interoceptive and exteroceptive stimuli, and that dysfunction of this serotonergic system contributes to an anxiety–like state and increases vulnerability to panic in animals and humans.

Key Words: panic, anxiety, serotonin, 5–HT, raphe, c–Fos, periaqueductal gray, sympathetic, autonomic

First published on February 28, 2008, doi:10.1177/0269881107082900

Journal of Psychopharmacology 2008;22:642.

A more recent version of this article appeared on August 1, 2008


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