{micro}-Opioid receptor agonist injections into the presumed pre-Botzinger complex and the surrounding region of awake goats do not alter eupneic breathing
1 Department of Physiology, Medical College of Wisconsin, ; 2 Department of Veterans Affairs Medical Center, and ; 3 Department of Physical Therapy, Marquette University, Milwaukee, Wisconsin Submitted 21 April 2008 ; accepted in final form 17 August 2009 Opioids are clinically important in the alle...
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Veröffentlicht in: | Journal of applied physiology (1985) 2009-11, Vol.107 (5), p.1591 |
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Sprache: | eng |
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Zusammenfassung: | 1 Department of Physiology, Medical College of Wisconsin, ;
2 Department of Veterans Affairs Medical Center, and ;
3 Department of Physical Therapy, Marquette University, Milwaukee, Wisconsin
Submitted 21 April 2008
; accepted in final form 17 August 2009
Opioids are clinically important in the alleviation of pain. An undesirable side effect of opioids is depression of breathing. Data from isolated preparations suggest this effect is due to attenuation of discharge activity of neurons in the pre-Bötzinger complex (preBötzC), a medullary area with respiratory rhythmogenic properties. The purpose of this study was to examine how [ D -Ala(2),N-Me-Phe(4),Gly(5)-ol]-enkephalin (DAMGO), a µ-opioid receptor agonist, affected breathing after injection into the presumed preBötzC of the adult awake goat. We hypothesized that DAMGO would cause breathing to decrease and become irregular when injected into the presumed preBötzC and the surrounding region of the conscious animal. We further hypothesized that ventilatory sensitivity to CO 2 and hypoxia would be blunted after the injection of DAMGO. Microtubules were bilaterally implanted into the presumed preBötzC of 10 adult female goats. After recovery from the surgery, DAMGO (0.5–10 µl, 1 nM–10 µM) was injected into the presumed preBötzC during the awake state. DAMGO had no effect on pulmonary ventilation [inspiratory minute ventilation ( I )], respiratory rhythm and pattern, the activation pattern of inspiratory and expiratory muscles, or arterial blood gases during eupneic breathing conditions ( P > 0.10). However, DAMGO attenuated ( P < 0.05) the evoked increase in breathing frequency when inspired CO 2 was increased, and DAMGO attenuated the I response to reduction of inspired O 2 to 10.8% ( P < 0.05). We conclude that our data do not provide support for the concept that in awake mammals opioid depression of breathing is due to a directed action of opioids on preBötzC neurons.
chemosensitivity; [ D -Ala(2),N-Me-Phe(4),Gly(5)-ol]-enkephalin
Address for reprint requests and other correspondence: K. L. Krause, 8701 Watertown Plank Rd., Milwaukee, WI 53226 (e-mail: klkrause{at}mcw.edu ). |
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ISSN: | 8750-7587 1522-1601 |
DOI: | 10.1152/japplphysiol.90548.2008 |