Reversible analgesia, atonia, and loss of consciousness on bilateral intracerebral microinjection of pentobarbital - PubMed (original) (raw)

Reversible analgesia, atonia, and loss of consciousness on bilateral intracerebral microinjection of pentobarbital

Marshall Devor et al. Pain. 2001 Oct.

Abstract

Concussion, asphyxia, and systemically administered general anesthetics all induce reversible depression of the organism's response to noxious stimuli as one of the elements of loss of consciousness. This is so even for barbiturate anesthetics, which have only modest analgesic efficacy at subanesthetic doses. Little is known about the neural circuits involved in this form of antinociception, although for anesthetic agents, at least, it is usually presumed that the drugs act in widely distributed regions of the nervous system. We now report the discovery of a focal zone in the brainstem mesopontine tegmentum in rats at which microinjection of minute quantities of pentobarbital induces a transient, reversible anesthetic-like state with non-responsiveness to noxious stimuli, flaccid atonia, and absence of the righting reflex. The behavioral suppression is accompanied by slow-wave EEG and, presumably, loss of consciousness. This zone, which we refer to as the mesopontine tegmental anesthesia locus (MPTA), apparently contains a barbiturate-sensitive 'switch' for both cortical and spinal activity. The very existence of the MPTA locus has implications for an understanding of the neural circuits that control motor functions and pain sensation, and for the cerebral representation of consciousness.

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References

    1. Basbaum A, Fields HL. Endogenous pain control systems: brainstem spinal pathways and endorphin circuitry. Annu Rev Neurosci. 1984;7:309-338.
    1. Bjorvatn B, Fagerland S, Ursin R. EEG power densities (0.5–20 Hz) in different sleep–wake stages in rats. Physiol Behav. 1998;63:413-417.
    1. Bland BD, Oddie SD. Anatomical, electrophysiological and pharmacological studies of ascending brainstem hippocampal synchronizing pathways. Neurosci Biobehav Rev. 1998;22:259-273.
    1. de Blas AL, Vitorica J, Friedrich P. Localization of the GABA-A receptor in the rat brain with a monoclonal antibody to the 57,000 Mr peptide of the GABA-A receptor/benzodiazepine receptor/Cl− channel complex. J Neurosci. 1988;8:602-614.
    1. Bolander H, Wahlstrom G, Norberg L. Reevaluation of potency and pharmacokinetic properties of some lipid-soluble barbiturates with an EEG-threshold method. Acta Pharmacol Toxicol (Copenh). 1984;54:33-40.

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