Opioid activities of human beta-casomorphins.

Standard

Opioid activities of human beta-casomorphins. / Koch, G; Wiedemann, Klaus; Teschemacher, H.

in: N-S ARCH PHARMACOL, Jahrgang 331, Nr. 4, 4, 1985, S. 351-354.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Koch, G, Wiedemann, K & Teschemacher, H 1985, 'Opioid activities of human beta-casomorphins.', N-S ARCH PHARMACOL, Jg. 331, Nr. 4, 4, S. 351-354. <http://www.ncbi.nlm.nih.gov/pubmed/3005882?dopt=Citation>

APA

Vancouver

Koch G, Wiedemann K, Teschemacher H. Opioid activities of human beta-casomorphins. N-S ARCH PHARMACOL. 1985;331(4):351-354. 4.

Bibtex

@article{6f1882ef7ba249d9ba4620eeadee55ab,
title = "Opioid activities of human beta-casomorphins.",
abstract = "Opioid activities of human beta-casomorphin-4, -5, -7 and -8 and, for comparison, of the corresponding bovine beta-casomorphins were studied in the guinea-pig ileum preparation. Binding parameters, i.e. KD-values and binding site concentrations, for the interaction of human and bovine beta-casomorphins with opioid receptors in rat brain homogenates were determined in inhibition experiments, using [3H]-(D-Ala2, MePhe4, Gly-ol5)enkephalin, [3H]-(D-Ala2, D-Leu5)enkephalin and [3H]ethylketazocin as mu-, delta- and kappa-opioid receptor ligands. Analysis of binding data was performed using a non-linear curve fitting program. All beta-casomorphins examined displayed opioid activity. The affinity was highest for mu-receptors, less so for delta-receptors and lowest for kappa-receptors. It is suggested that human beta-casomorphins might play a role as {"}food hormones{"}.",
author = "G Koch and Klaus Wiedemann and H Teschemacher",
year = "1985",
language = "Deutsch",
volume = "331",
pages = "351--354",
journal = "N-S ARCH PHARMACOL",
issn = "0028-1298",
publisher = "Springer",
number = "4",

}

RIS

TY - JOUR

T1 - Opioid activities of human beta-casomorphins.

AU - Koch, G

AU - Wiedemann, Klaus

AU - Teschemacher, H

PY - 1985

Y1 - 1985

N2 - Opioid activities of human beta-casomorphin-4, -5, -7 and -8 and, for comparison, of the corresponding bovine beta-casomorphins were studied in the guinea-pig ileum preparation. Binding parameters, i.e. KD-values and binding site concentrations, for the interaction of human and bovine beta-casomorphins with opioid receptors in rat brain homogenates were determined in inhibition experiments, using [3H]-(D-Ala2, MePhe4, Gly-ol5)enkephalin, [3H]-(D-Ala2, D-Leu5)enkephalin and [3H]ethylketazocin as mu-, delta- and kappa-opioid receptor ligands. Analysis of binding data was performed using a non-linear curve fitting program. All beta-casomorphins examined displayed opioid activity. The affinity was highest for mu-receptors, less so for delta-receptors and lowest for kappa-receptors. It is suggested that human beta-casomorphins might play a role as "food hormones".

AB - Opioid activities of human beta-casomorphin-4, -5, -7 and -8 and, for comparison, of the corresponding bovine beta-casomorphins were studied in the guinea-pig ileum preparation. Binding parameters, i.e. KD-values and binding site concentrations, for the interaction of human and bovine beta-casomorphins with opioid receptors in rat brain homogenates were determined in inhibition experiments, using [3H]-(D-Ala2, MePhe4, Gly-ol5)enkephalin, [3H]-(D-Ala2, D-Leu5)enkephalin and [3H]ethylketazocin as mu-, delta- and kappa-opioid receptor ligands. Analysis of binding data was performed using a non-linear curve fitting program. All beta-casomorphins examined displayed opioid activity. The affinity was highest for mu-receptors, less so for delta-receptors and lowest for kappa-receptors. It is suggested that human beta-casomorphins might play a role as "food hormones".

M3 - SCORING: Zeitschriftenaufsatz

VL - 331

SP - 351

EP - 354

JO - N-S ARCH PHARMACOL

JF - N-S ARCH PHARMACOL

SN - 0028-1298

IS - 4

M1 - 4

ER -