Literature DB >> 12717134

Peri-MAC depression of a nociceptive withdrawal reflex is accompanied by reduced dorsal horn activity with halothane but not isoflurane.

Steven L Jinks1, John T Martin, Earl Carstens, Sung-Won Jung, Joseph F Antognini.   

Abstract

BACKGROUND: Anesthetics act in the spinal cord to suppress movement evoked by a noxious stimulus, although the exact site is unknown.
METHODS: This study investigated sensorimotor processing in hind limb withdrawal reflexes, and effects of two general anesthetics, halothane and isoflurane, on simultaneously recorded responses of single dorsal horn neurons and hind limb withdrawal force, elicited by graded noxious thermal hind paw stimulation in rats. Minimum alveolar anesthetic concentration (MAC) needed to block gross movement to a supra-maximal mechanical stimulus was determined for each animal.
RESULTS: Between 0.9 and 1.1 MAC, halothane and isoflurane greatly reduced or abolished withdrawal force (79 and 89% reduction, respectively). Halothane (0.75-1.4 MAC) depressed heat-evoked neuronal responses in a concentration-related manner (41% reduction between 0.9 and 1.1 MAC averaged across all stimulus temperatures, P < 0.05) and decreased stimulus-response function slopes, with corresponding reductions in withdrawal force. In contrast, isoflurane did not reduce neuronal responses in the 0.75-1.4 MAC range and slightly facilitated responses (by 16%) when concentration increased from 0.9 to 1.1 MAC, despite a concurrent withdrawal force reduction. Anesthetic depression of heat-evoked withdrawal force correlated well with MAC determination using a supra-maximal mechanical stimulus. At sub-MAC anesthetic concentrations, some units exhibited firing rate changes that preceded and paralleled moment-to-moment changes in force during a given withdrawal.
CONCLUSIONS: Halothane reduces noxious-evoked movement at least partly via depression of dorsal horn neurons, whereas isoflurane suppresses movement by an action at more ventral sites in the spinal cord.

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Year:  2003        PMID: 12717134     DOI: 10.1097/00000542-200305000-00015

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  16 in total

1.  Volatile anesthetic effects on midbrain-elicited locomotion suggest that the locomotor network in the ventral spinal cord is the primary site for immobility.

Authors:  Steven L Jinks; Milo Bravo; Shawn G Hayes
Journal:  Anesthesiology       Date:  2008-06       Impact factor: 7.892

2.  A method for recording single unit activity in lumbar spinal cord in rats anesthetized with nitrous oxide in a hyperbaric chamber.

Authors:  Joseph F Antognini; Richard J Atherley; Michael J Laster; Earl Carstens; Robert C Dutton; Edmond I Eger
Journal:  J Neurosci Methods       Date:  2006-10-11       Impact factor: 2.390

3.  Isoflurane and sevoflurane decrease entropy indices more than halothane at equal MAC values.

Authors:  Hemanshu Prabhakar; Zulfiqar Ali; Parmod K Bithal; Girija P Rath; Deepak Singh; Hari H Dash
Journal:  J Anesth       Date:  2009-02-22       Impact factor: 2.078

4.  Rat dorsal horn nociceptive-specific neurons are more sensitive than wide dynamic range neurons to depression by immobilizing doses of volatile anesthetics: an effect partially reversed by the opioid receptor antagonist naloxone.

Authors:  Linda S Barter; Earl E Carstens; Steven L Jinks; Joseph F Antognini
Journal:  Anesth Analg       Date:  2009-08       Impact factor: 5.108

5.  Immobilizing doses of halothane, isoflurane or propofol, do not preferentially depress noxious heat-evoked responses of rat lumbar dorsal horn neurons with ascending projections.

Authors:  Linda S Barter; Laurie O Mark; Steven L Jinks; Earl E Carstens; Joseph F Antognini
Journal:  Anesth Analg       Date:  2008-03       Impact factor: 5.108

6.  Nitrous oxide-induced analgesia does not influence nitrous oxide's immobilizing requirements.

Authors:  Steven L Jinks; Earl Carstens; Joseph F Antognini
Journal:  Anesth Analg       Date:  2009-10       Impact factor: 5.108

7.  Neurons in the ventral spinal cord are more depressed by isoflurane, halothane, and propofol than are neurons in the dorsal spinal cord.

Authors:  JongBun Kim; Aubrey Yao; Richard Atherley; Earl Carstens; Steven L Jinks; Joseph F Antognini
Journal:  Anesth Analg       Date:  2007-10       Impact factor: 5.108

8.  Brainstem regions affecting minimum alveolar concentration and movement pattern during isoflurane anesthesia.

Authors:  Steven L Jinks; Milo Bravo; Omar Satter; Yuet-Ming Chan
Journal:  Anesthesiology       Date:  2010-02       Impact factor: 7.892

9.  Differential effects of isoflurane and propofol on upper airway dilator muscle activity and breathing.

Authors:  Matthias Eikermann; Atul Malhotra; Philipp Fassbender; Sebastian Zaremba; Amy S Jordan; Shiva Gautam; David P White; Nancy L Chamberlin
Journal:  Anesthesiology       Date:  2008-05       Impact factor: 7.892

10.  Isoflurane anesthesia does not affect spinal cord neurovascular coupling: evidence from decerebrated rats.

Authors:  Thierry Paquette; Hugues Leblond; Mathieu Piché
Journal:  J Physiol Sci       Date:  2018-03-29       Impact factor: 2.781

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