Phosphodiesterase 4 (PDE4) and neurological disorders: A promising frontier in neuropharmacology.

Q1 Pharmacology, Toxicology and Pharmaceutics
Advances in pharmacology Pub Date : 2025-01-01 Epub Date: 2024-10-22 DOI:10.1016/bs.apha.2024.10.005
Sumaiya Nahid, Saeedeh Saeedi, Corey R Hopkins
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引用次数: 0

Abstract

The phosphodiesterase 4 (PDE4) enzyme plays a crucial role in the central nervous system (CNS). It is extensively expressed in mammalian brain, where it regulates intracellular cyclic adenosine monophosphate (cAMP) levels. Dysregulation of PDE4 and cAMP balance is associated with various neurodegenerative diseases. By inhibiting PDE4 with drugs, cAMP levels can be stabilized, potentially improving symptoms in mental and neurological disorders such as cognition, depression, and Parkinson's disease. Mechanistically, PDE4 inhibitors exert anti-inflammatory and neuroprotective effects by increasing cAMP accumulation and activating protein kinase A (PKA). This chapter will review the relevant neurological disorders that PDE4 has been associated with and review the preclinical and clinical studies.

磷酸二酯酶4 (PDE4)与神经系统疾病:神经药理学的一个有前途的前沿。
磷酸二酯酶4 (PDE4)在中枢神经系统中起着至关重要的作用。它在哺乳动物大脑中广泛表达,调节细胞内环磷酸腺苷(cAMP)水平。PDE4和cAMP平衡失调与多种神经退行性疾病有关。通过药物抑制PDE4,可以稳定cAMP水平,潜在地改善认知、抑郁和帕金森病等精神和神经疾病的症状。从机制上讲,PDE4抑制剂通过增加cAMP积累和激活蛋白激酶A (PKA)来发挥抗炎和神经保护作用。本章将回顾与PDE4相关的神经系统疾病,并回顾临床前和临床研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in pharmacology
Advances in pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
9.10
自引率
0.00%
发文量
45
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