Zobrazeno 1 - 10
of 13
pro vyhledávání: '"J J, Rady"'
Publikováno v:
Proceedings of the Society for Experimental Biology and Medicine. 224:93-101
Heroin produced antinociception in the tail flick test through mu receptors in the brain of ICR and CD-1 mice, a response inhibited by 3-O-methylnaltrexone. Tolerance to morphine was produced by subcutaneous morphine pellet implantation. By the third
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8b49c55325089c85c10fd076a6ac5a5
https://doi.org/10.1046/j.1525-1373.2000.22406.x
https://doi.org/10.1046/j.1525-1373.2000.22406.x
Publikováno v:
Experimental Biology and Medicine. 220:178-183
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d613bb0f0af11d589f2342860ec397bc
https://doi.org/10.3181/00379727-220-44361
https://doi.org/10.3181/00379727-220-44361
Autor:
J J, Rady, J M, Fujimoto
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 299(2)
Spinal dynorphin A(1-17) (Dyn) has been shown previously to produce an antianalgesic action against intrathecal morphine in the tail-flick test in CD-1 mice. This action is known to be mediated indirectly from the spinal cord through an afferent path
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a5c446f0bdef51d96a1ec48b6d9aed4f
https://pubmed.ncbi.nlm.nih.gov/11602679
https://pubmed.ncbi.nlm.nih.gov/11602679
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 297(2)
Dynorphin A(1-17) given intrathecally releases spinal cholecystokinin to produce an antianalgesic action against spinal morphine in the tail-flick test in CD-1 mice. The present study showed that following the cholecystokinin step, a delta(2)-opioid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::618aba84ccd5f667a728779cb7e828d3
https://pubmed.ncbi.nlm.nih.gov/11303046
https://pubmed.ncbi.nlm.nih.gov/11303046
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 296(1)
An antianalgesic action of intracerebroventricularly administered nociceptin was elicited against intrathecal morphine-induced antinociception in the tail-flick test in mice and investigated as a descending neuronal system for the spinal mediator inv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::380018f21307bae5a69da74fd183dd9e
https://pubmed.ncbi.nlm.nih.gov/11123356
https://pubmed.ncbi.nlm.nih.gov/11123356
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 288(2)
Heroin administered i.c.v. acts on supraspinal mu opioid receptors in ICR mice but on delta receptors in Swiss Webster mice. The purpose of this study was to determine the degree to which genotype plays a role in the opioid receptor selectivity of he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ed64dd7007d29efa17bf3f255c9030e3
https://pubmed.ncbi.nlm.nih.gov/9918543
https://pubmed.ncbi.nlm.nih.gov/9918543
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 284(3)
Pentobarbital administered intracerebroventricularly to mice has been shown previously to inhibit the analgesic action of morphine given intrathecally. The purpose of the present study was to examine the proposal that this antianalgesic action was me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f4ce9d4f1878d85ad9bbaefdb4c45a6e
https://pubmed.ncbi.nlm.nih.gov/9495845
https://pubmed.ncbi.nlm.nih.gov/9495845
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 268(3)
Heroin activates delta receptors, whereas morphine activates mu receptors, in the brain of Swiss-Webster mice, to produce antinociception. The present study determined the type of opioid receptor activated by 6-monoacetylmorphine (MAM), a metabolite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::551e0d5f1687012c7b4ee7e7d07ed0c6
https://pubmed.ncbi.nlm.nih.gov/8138935
https://pubmed.ncbi.nlm.nih.gov/8138935
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 268(2)
Previous studies in mice demonstrate that, when dynorphin A (1-17) (Dyn A) is administered intrathecally (i.t.) or released spinally (by administration of clonidine or midazolam i.c.v.), i.t. morphine-induced analgesia was reduced. The present aim wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ddd24ba9ab6094ca33a0d8c477e6a1b7
https://pubmed.ncbi.nlm.nih.gov/7906735
https://pubmed.ncbi.nlm.nih.gov/7906735
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 259(3)
In recent publications we have proposed that dynorphin (Dyn) A(1-17) functions as an antianalgesic modulator to oppose opioid-induced antinociception in mice. In the present experiments using the tail-flick response in mice, other Dyns [Dyn A(1-8), D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52a09fa434ce2a9926d04b0cc42f4ce7
https://pubmed.ncbi.nlm.nih.gov/1684812
https://pubmed.ncbi.nlm.nih.gov/1684812