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Chinese Journal of Clinical Pharmacology and Therapeutics ›› 2008, Vol. 13 ›› Issue (6): 711-715.

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Phosphodiesterase 3: new targets for drug development

YE Yi-lu, ZHANG Qi, YU Yue-ping   

  1. Department of Pharmacology, Zhejiang Medical College, Hangzhou 310053, Zhejiang, China
  • Received:2008-01-22 Revised:2008-04-08 Published:2020-10-14

Abstract: Phosphodiesterase (PDE) is hydrolase of 3', 5'-cyclic adenosine monophosphate (cAMP) and 3', 5'-cyclic guanosine monophosphate (cGMP). PDE3 are composed of two genes and distributed widely in vivo.Its inhibitors have been applied in antiplatelet aggregation and vasodilation.It has been reported that PDE3 inhibitors have neuroprotective effects on cerebral ischemia, which may provide new methods to prevention and therapy of cerebral ischemia.

Key words: phosphodiesterase (PDE), neuroprotection, cerebral ischemia

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