Novel radioiodinated γ-hydroxybutyric acid analogues for radiolabeling and photolinking of high-affinity γ-hydroxybutyric acid binding sites
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Novel radioiodinated γ-hydroxybutyric acid analogues for radiolabeling and photolinking of high-affinity γ-hydroxybutyric acid binding sites. / Wellendorph, Petrine; Høg, Signe; Sabbatini, Paola; Pedersen, Martin Holst Friborg; Martiny, Lars; Knudsen, Gitte Moos; Frølund, Bente Flensborg; Clausen, Rasmus Prætorius; Bräuner-Osborne, Hans.
I: Journal of Pharmacology and Experimental Therapeutics, Bind 335, Nr. 2, 2010, s. 458-464.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Novel radioiodinated γ-hydroxybutyric acid analogues for radiolabeling and photolinking of high-affinity γ-hydroxybutyric acid binding sites
AU - Wellendorph, Petrine
AU - Høg, Signe
AU - Sabbatini, Paola
AU - Pedersen, Martin Holst Friborg
AU - Martiny, Lars
AU - Knudsen, Gitte Moos
AU - Frølund, Bente Flensborg
AU - Clausen, Rasmus Prætorius
AU - Bräuner-Osborne, Hans
PY - 2010
Y1 - 2010
N2 - gamma-Hydroxybutyric acid (GHB) is a therapeutic drug, a drug of abuse and an endogenous substance that binds to low and high-affinity sites in the mammalian brain. To target the specific GHB binding sites, we have developed a (125)I-labeled GHB analogue and characterized its binding in rat brain homogenate and slices. Our data show that [(125)I]BnOPh-GHB binds to one site in rat brain cortical membranes with low nanomolar affinity (K(d) 7 nM, B(max) 61 pmol/mg protein). The binding is inhibited by GHB and selected analogues, but not by GABA. Autoradiography using horizontal slices from rat brain demonstrates the highest density of binding in hippocampus and cortical regions and the lowest density in the cerebellum. Altogether the findings correlate with the labeling and brain regional distribution of high-affinity GHB sites or [(3)H](E,RS)-(6,7,8,9-tetrahydro-5-hydroxy-5H-benzocyclohept-6-ylidene)acetic acid ([(3)H]NCS-382) binding sites. Using a (125)I-labeled photoaffinity derivative of the new GHB ligand, we have performed denaturing protein electrophoresis and detected one major protein band with an apparent weight of 50 kDa from cortical and hippocampal membranes. [(125)I]BnOPh-GHB is the first reported (125)I-labeled GHB radioligand and is a useful tool for in vitro studies of the specific high-affinity GHB binding sites. The related photoaffinity linker [(125)I]azido-BnOPh-GHB can be used as a probe for isolation of the elusive GHB binding protein.
AB - gamma-Hydroxybutyric acid (GHB) is a therapeutic drug, a drug of abuse and an endogenous substance that binds to low and high-affinity sites in the mammalian brain. To target the specific GHB binding sites, we have developed a (125)I-labeled GHB analogue and characterized its binding in rat brain homogenate and slices. Our data show that [(125)I]BnOPh-GHB binds to one site in rat brain cortical membranes with low nanomolar affinity (K(d) 7 nM, B(max) 61 pmol/mg protein). The binding is inhibited by GHB and selected analogues, but not by GABA. Autoradiography using horizontal slices from rat brain demonstrates the highest density of binding in hippocampus and cortical regions and the lowest density in the cerebellum. Altogether the findings correlate with the labeling and brain regional distribution of high-affinity GHB sites or [(3)H](E,RS)-(6,7,8,9-tetrahydro-5-hydroxy-5H-benzocyclohept-6-ylidene)acetic acid ([(3)H]NCS-382) binding sites. Using a (125)I-labeled photoaffinity derivative of the new GHB ligand, we have performed denaturing protein electrophoresis and detected one major protein band with an apparent weight of 50 kDa from cortical and hippocampal membranes. [(125)I]BnOPh-GHB is the first reported (125)I-labeled GHB radioligand and is a useful tool for in vitro studies of the specific high-affinity GHB binding sites. The related photoaffinity linker [(125)I]azido-BnOPh-GHB can be used as a probe for isolation of the elusive GHB binding protein.
KW - Faculty of Health and Medical Sciences
U2 - 10.1124/jpet.110.170670
DO - 10.1124/jpet.110.170670
M3 - Journal article
C2 - 20696866
VL - 335
SP - 458
EP - 464
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
SN - 0022-3565
IS - 2
ER -
ID: 21772160