Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Maynard H. Makman"'
Autor:
Thomas V. Bilfinger, Yu Liu, Berta Scharrer, Gregory L. Fricchione, Harold I. Magazine, Maynard H. Makman, Eric M. Smith, Thomas K. Hughes, George B. Stefano, Alan R. Hartman
Publikováno v:
Europe PubMed Central
The discovery of the ability of the nervous system to communicate through "public" circuits with other systems of the body is attributed to Ernst and Berta Scharrer, who described the neurosecretory process in 1928. Indeed, the immune system has been
Autor:
B. Dvorkin, Maynard H. Makman
Publikováno v:
European Journal of Pharmacology. 338:171-176
Nociceptin (orphanin FQ), a heptadecapeptide with some sequence homology to dynorphin A, has been proposed as an endogenous ligand for a previously cloned orphan receptor with significant homology to opioid receptors. Utilizing [(125)I][Tyr14]nocicep
Publikováno v:
Brain Research. 686:239-248
Evidence is presented for occurrence of opiate alkaloid-selective, opioid-peptide-insensitive receptor binding sites, labeled with [3H]morphine, in primary cultures of cat microglia and of cat astrocytes, as well as on highly purified preparations of
Autor:
Maynard H. Makman
Publikováno v:
Advances in Neuroimmunology. 4:69-82
Receptor interactions of morphine are reviewed, with particular attention given to a recently discovered opiate receptor, designated mu 3, with unique selectivity for morphine and certain other opiate alkaloids. Morphine, other opiate alkaloids and r
Publikováno v:
Endocrinology. 133:2818-2826
The responsiveness of adenylyl cyclase to beta-adrenergic receptor stimulation was investigated in membranes prepared from hypothalamus-preoptic area and cortex of ovariectomized female rats injected with oil vehicle or estradiol benzoate 24 or 48 h
Autor:
Naji N. Abumrad, Michael K. Leung, Thomas V. Bilfinger, George B. Stefano, Berta Scharrer, Maynard H. Makman, Alex Digenis, Sydney Spector
Publikováno v:
Proceedings of the National Academy of Sciences. 90:11099-11103
The presence of morphine-like and codeine-like substances was demonstrated in the pedal ganglia, hemolymph, and mantle tissues of the mollusc Mytilus edulis. The pharmacological activities of the endogenous morphine-like material resemble those of au
Publikováno v:
Neuropharmacology. 31:799-807
Treatment of ovariectomized rats with both estradiol and progesterone in vivo resulted in a marked enhancement of glutamate-induced release of newly synthesized [ 3 H]γ-aminobutyric acid (GABA) from synaptosomes of the preoptic area in vitro . With
Publikováno v:
Neuroscience letters. 269(1)
l -Prolyl- l -leucyl-glycinamide (PLG), also known as melanocyte-stimulating hormone release inhibiting factor (MIF-1), is an endogenous brain tripeptide. Previous studies have shown that PLG, and its peptidomimetic analogues, render dopamine D 2 rec
Publikováno v:
Brain Research. 507:161-163
In vivo treatment of ovariectomized rats with estradiol benzoate plus progesterone, but not with either steroid alone, produced a large increase in veratridine-induced release of radiolabeled glutamate and newly synthesized GABA from preoptic area sy
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461374398
An opiate alkaloid-selective receptor, designated µ3, mediates inhibition by morphine of activation of human peripheral blood monocytes and granulocytes. The µ3receptor is present on several macrophage cell types including microglia, on cultured as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3395981c8d53cced232acbf2ded0df24
https://doi.org/10.1007/978-1-4615-5347-2_15
https://doi.org/10.1007/978-1-4615-5347-2_15