التفاصيل البيبلوغرافية
العنوان: |
Assessment of [125I]WYE-230949 as a Novel Histamine H3 Receptor Radiopharmaceutical. |
المؤلفون: |
Lewis, David Y., Champion, Sue, Wyper, David, Dewar, Deborah, Pimlott, Sally |
المصدر: |
PLoS ONE; Dec2014, Vol. 9 Issue 12, p1-19, 19p |
مصطلحات موضوعية: |
HISTAMINE receptors, RADIOPHARMACEUTICALS, SCHIZOPHRENIA treatment, TREATMENT of attention-deficit hyperactivity disorder, OBESITY, ALZHEIMER'S disease, RADIONUCLIDE imaging |
مستخلص: |
Histamine H3 receptor therapeutics have been proposed for several diseases such as schizophrenia, attention deficit hyperactivity disorder, Alzheimer's disease and obesity. We set out to evaluate the novel compound, [125I]WYE-230949, as a potential radionuclide imaging agent for the histamine H3 receptor in brain. [125I]WYE-230949 had a high in vitro affinity for the rat histamine H3 receptor (Kd of 6.9 nM). The regional distribution of [125I]WYE-230949 binding sites in rat brain, demonstrated by in vitro autoradiography, was consistent with the known distribution of the histamine H3 receptor. Rat brain uptake of intravenously injected [125I]WYE-230949 was low (0.11 %ID/g) and the ratio of specific: non-specific binding was less than 1.4, as determined by ex vivo autoradiography. In plasma, metabolism of [125I]WYE-230949 into a less lipophilic species occurred, such that less than 38% of the parent compound remained 30 minutes after injection. Brain uptake and metabolism of [125I]WYE-230949 were increased and specific binding was reduced in anaesthetised compared to conscious rats. [125I]WYE230949 is not a potential radiotracer for imaging rat histamine H3 receptors in vivo due to low brain uptake, in vivo metabolism of the parent compound and low specific binding. [ABSTRACT FROM AUTHOR] |
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قاعدة البيانات: |
Complementary Index |