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Opioid depression of respiration in neonatal rats
1. The effects of opioid receptor agonists and antagonists on the breathing pattern of neonatal rats were studied. Three experimental approaches were taken. In the first approach, the effects of opioid agonists and antagonists on the spontaneous respiratory neural activity generated by brainstem-spi...
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Published in: | The Journal of physiology 1995-06, Vol.485 (Pt 3), p.845-855 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | 1. The effects of opioid receptor agonists and antagonists on the breathing pattern of neonatal rats were studied. Three experimental
approaches were taken. In the first approach, the effects of opioid agonists and antagonists on the spontaneous respiratory
neural activity generated by brainstem-spinal cords isolated from neonatal rats aged 0-4 days postnatal (P0-4) maintained
in vitro were studied. Secondly, similar studies were performed utilizing medullary slice preparations consisting of respiratory
rhythm-generating regions (pre-Bötzinger complex). Thirdly, whole-body plethysmographic recordings were obtained from unanaesthetized
neonatal (P0-18) rats before and after I.P. administration of opioid-receptor agonists and antagonists. 2. The mu-receptor
agonists morphiceptin and DAGO (Tyr-D-Ala-Gly-[NMePhe]-Gly-ol), when added either to the solutions bathing the brainstems
of neonatal rat brainstem-spinal cord preparations or bathing the medullary slice preparations, resulted in a naloxone-reversible,
dose-dependent decrease in the frequency of respiratory rhythmic discharge. 3. The respiratory burst frequency and amplitude
in vitro were unaffected by the addition of the delta-opioid receptor agonist DPDPE ([D-pen2,5]-enkephalin) and the kappa-opioid
receptor agonist U50488 (trans-[+]-3,4-dichloro-N-methyl-N-(2-[1- pyrrolidinyl]cyclohexyl) benzene-acetamide) or the opioid
receptor antagonist naloxone. 4. Intraperitoneal administration of the mu-opioid receptor agonist fentanyl resulted in a naloxone-reversible,
dose-dependent decrease in the frequency and amplitude of breathing of unanaesthetized neonatal rats (P0-P10). I.P. administration
of the delta-opioid receptor agonist DPDPE did not affect breathing of neonatal rats until the second week postnatally. 5.
We conclude that opioids suppress the frequency of neonatal rat respiration by acting via mu-opioid receptors located within
regions of the ventral medulla containing respiratory rhythm-generating centres (the pre-Bötzinger complex). delta-Opioid
receptor activation does not affect breathing in neonatal rats until approximately the second week postnatally. |
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ISSN: | 0022-3751 1469-7793 |
DOI: | 10.1113/jphysiol.1995.sp020774 |