4.7 Article

Modulation of D-serine levels in brains of mice lacking PICK1

期刊

BIOLOGICAL PSYCHIATRY
卷 63, 期 10, 页码 997-1000

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.biopsych.2007.09.025

关键词

bipolar disorder; D-serine; knockout mice; PICK1; schizophrenia; serine racemase

资金

  1. Howard Hughes Medical Institute Funding Source: Medline
  2. NIDA NIH HHS [DA00074, K05 DA000074] Funding Source: Medline
  3. NIMH NIH HHS [R01 MH018501, 1 F30 MH074191-01A2, F30 MH074191, R37 MH018501, MH069853, MH18501, R01 MH069853] Funding Source: Medline
  4. NINDS NIH HHS [R01 NS036715-08, NS036715, R01 NS036715] Funding Source: Medline

向作者/读者索取更多资源

Background: D-serine is an endogenous coagonist of the N-methyl-D-aspartate subtype glutamate receptor. Genetic association studies have implicated genes coding for enzymes associated with D-serine metabolism in schizophrenia and bipolar disorder. Methods: Protein expression of serine racemase (SR) and its binding partner, protein interacting with C-kinase (PICK1), were examined by Western blotting in brains from wildtype and PICK1 knockout mice. Levels of D-serine in wildtype and PICK1 mice were also examined by an established high-pressure liquid chromatography protocol. Results: Expression of SR and PICK1 proteins was developmentally regulated. Although no change was observed in the level of SR protein, levels of D-serine were selectively decreased in the forebrain of neonatal PICK1 knockout mice, compared with those in wildtype mice. Conclusions: PICK1 may be involved in the regulation of brain D-serine levels and SR in a spatially and temporally specific manner.

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