Zobrazeno 1 - 10
of 32
pro vyhledávání: '"S F Maier"'
Autor:
E D, Milligan, V, Zapata, M, Chacur, D, Schoeniger, J, Biedenkapp, K A, O'Connor, G M, Verge, G, Chapman, P, Green, A C, Foster, G S, Naeve, S F, Maier, L R, Watkins
Publikováno v:
The European journal of neuroscience. 20(9)
Recent evidence suggests that spinal cord glia can contribute to enhanced nociceptive responses. However, the signals that cause glial activation are unknown. Fractalkine (CX3C ligand-1; CX3CL1) is a unique chemokine expressed on the extracellular su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccd2dbfbcdebb2e0af0f1f6848ec8050
https://pubmed.ncbi.nlm.nih.gov/15525271
https://pubmed.ncbi.nlm.nih.gov/15525271
Publikováno v:
Behavioral neuroscience. 113(4)
Inescapable shock (IS) enhances analgesia to systemic morphine (MOR) 24 hr later. IS activates serotonin neurons in the dorsal raphe nucleus (DRN), rendering them hyperexcitable. These studies tested whether IS potentiates the analgesic effect of MOR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::704fd0c39d4def4af2c5ab1caccc41b5
https://pubmed.ncbi.nlm.nih.gov/10495087
https://pubmed.ncbi.nlm.nih.gov/10495087
Publikováno v:
Advances in experimental medicine and biology. 461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c95853e3f291e4a0b2c4f768a256c50a
https://pubmed.ncbi.nlm.nih.gov/10442176
https://pubmed.ncbi.nlm.nih.gov/10442176
Publikováno v:
Advances in experimental medicine and biology. 461
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b94389e37cd9705014d73f2a58a64680
https://pubmed.ncbi.nlm.nih.gov/10442173
https://pubmed.ncbi.nlm.nih.gov/10442173
Publikováno v:
Journal of neuroendocrinology. 11(2)
Many stressors elicit changes in corticotrophin (CRH), enkephalin (ENK), and neurotensin (NT) mRNA levels within the medial parvocellular region of the paraventricular nucleus of the hypothalamus (mpPVN), and the pattern of changes in mRNA levels app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6106291cadcaf0e9d0f7242ae5b3df6e
https://pubmed.ncbi.nlm.nih.gov/10048467
https://pubmed.ncbi.nlm.nih.gov/10048467
Autor:
T, Deak, K T, Nguyen, A L, Ehrlich, L R, Watkins, R L, Spencer, S F, Maier, J, Licinio, M L, Wong, G P, Chrousos, E, Webster, P W, Gold
Publikováno v:
Endocrinology. 140(1)
The nonpeptide CRH antagonist antalarmin has been shown to block both behavioral and endocrine responses to CRH. However, it's potential activity in blunting behavioral and endocrine sequelae of stressor exposure has not been assessed. Because antago
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::62dc8db38ad74931f84d4996dfb2e683
https://pubmed.ncbi.nlm.nih.gov/9886810
https://pubmed.ncbi.nlm.nih.gov/9886810
Publikováno v:
Behavioral neuroscience. 112(2)
Pain inhibition (analgesia) is produced by learned danger signals and inhibited by learned safety signals (antianalgesia). Conditioned analgesia is mediated by brain-to-spinal pathways releasing spinal endogenous opiates. Spinal morphine mimics learn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ba4e30c6b42ef3863a54e21ac2370709
https://pubmed.ncbi.nlm.nih.gov/9588483
https://pubmed.ncbi.nlm.nih.gov/9588483
Autor:
L C, Sutton, S E, Lea, M J, Will, B A, Schwartz, C E, Hartley, J C, Poole, L R, Watkins, S F, Maier
Publikováno v:
Behavioral neuroscience. 111(5)
Exposure to various stressors potentiates nociceptive and nonnociceptive responses to morphine. These phenomena have received little study despite their seeming generality and importance for understanding analgesia and opiate action. The present expe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aa808a217cd95a28698642ac73fee311
https://pubmed.ncbi.nlm.nih.gov/9383528
https://pubmed.ncbi.nlm.nih.gov/9383528
Publikováno v:
Behavioral neuroscience. 111(4)
Exposure of rats to inescapable shock (IS) potentiated the analgesic response to a low dose (1 mg/kg) of morphine 24 hr later. This effect was blocked by naltrexone (10 micrograms), diazepam (5 micrograms), or 8-hydroxy-2-(di-n-propylamine)-tetralin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::33c5ea4b5f170957e0e249fa15909f7d
https://pubmed.ncbi.nlm.nih.gov/9267659
https://pubmed.ncbi.nlm.nih.gov/9267659