Phosphodiesterase 9A in Brain Regulates cGMP Signaling Independent of Nitric-Oxide

被引:18
|
作者
Harms, John F. [1 ]
Menniti, Frank S. [2 ]
Schmidt, Christopher J. [3 ]
机构
[1] Pfizer Global Res & Dev, Internal Med Res Unit, Cambridge, MA USA
[2] Univ Rhode Isl, George Anne Ryan Inst Neurosci, Kingston, RI 02881 USA
[3] Pfizer Global Res & Dev, Pfizer Innovat & Res Lab Unit, Cambridge, MA 02139 USA
关键词
cGMP; PDE9A; phosphodiesterase inhibitor; nitric oxide; nitric oxide synthase; brain; cognitive disorders; PDE9 INHIBITOR PF-04447943; MESSENGER-RNA; NATRIURETIC PEPTIDES; SYNAPTIC PLASTICITY; MICE DEFICIENT; LOCALIZATION; SYNTHASE; PDE10A; IDENTIFICATION; EXPRESSION;
D O I
10.3389/fnins.2019.00837
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
PDE9A is a cGMP-specific phosphodiesterase expressed in neurons throughout the brain that has attracted attention as a therapeutic target to treat cognitive disorders. Indeed, PDE9A inhibitors are under evaluation in clinical trials as a treatment for Alzheimer's disease and schizophrenia. However, little is known about the cGMP signaling cascades regulated by PDE9A. Canonical cGMP signaling in brain follows the activation of neuronal nitric oxide synthase (nNOS) and the generation of nitric oxide, which activates soluble guanylyl cyclase and cGMP synthesis. However, we show that in mice, PDE9A regulates a pool of cGMP that is independent of nNOS, specifically, and nitric oxide signaling in general. This PDE9A-regulated cGMP pool appears to be highly compartmentalized and independent of cGMP pools regulated by several PDEs. These findings provide a new foundation for study of the upstream and downstream signaling elements regulated by PDE9A and its potential as a therapeutic target for brain disease.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] NITRIC-OXIDE REGULATES SPIKE FREQUENCY ACCOMMODATION IN NODOSE NEURONS OF THE RABBIT
    COHEN, AS
    WEINREICH, D
    KAO, JPY
    NEUROSCIENCE LETTERS, 1994, 173 (1-2) : 17 - 20
  • [32] NITRIC-OXIDE REGULATES THE CALCIUM CURRENT IN ISOLATED HUMAN ATRIAL MYOCYTES
    KIRSTEIN, M
    RIVETBASTIDE, M
    HATEM, S
    BENARDEAU, A
    MERCADIER, JJ
    FISCHMEISTER, R
    JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (02) : 794 - 802
  • [33] cGMP-dependent and -independent properties of nitric angiogenesis-related oxide
    Pyriochou, Anastasia
    Vassilakopoulos, Theodoros
    Zhou, Zongmin
    Papapetropoulos, Andreas
    LIFE SCIENCES, 2007, 81 (21-22) : 1549 - 1554
  • [34] A novel phosphodiesterase 9A inhibitor LW33 protects against ischemic stroke through the cGMP/PKG/CREB pathway
    You, Jia-yi
    Liu, Xin-wei
    Bao, Ying-xia
    Shen, Zheng-nan
    Wang, Quan
    He, Gong-yun
    Lu, Jing
    Zhang, Ji-guo
    Chen, Jian-wen
    Liu, Pei-qing
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2022, 925
  • [35] NITRIC-OXIDE REGULATES CEREBRAL ARTERIOLAR TONE IN RATS
    KIMURA, M
    DIETRICH, HH
    DACEY, RG
    STROKE, 1994, 25 (11) : 2227 - 2233
  • [36] Effects of tetramethylpyrazine on nitric oxide/cGMP signaling after cerebral vasospasm in rabbits
    Shao, Zhengkai
    Li, Jingwen
    Zhao, Zhenhuan
    Gao, Cheng
    Sun, Zhe
    Liu, Xiangzhen
    BRAIN RESEARCH, 2010, 1361 : 67 - 75
  • [37] 17β-Estradiol Inhibites Nitric Oxide-cGMP-Dependent Pathway but may Activate Independent Pathway in Small Intestinum of Ovariectomized Rat
    Sevimli, Sevcan
    Bulbul, Aziz
    KAFKAS UNIVERSITESI VETERINER FAKULTESI DERGISI, 2013, 19 (06) : 949 - 954
  • [38] 5-Hydroxytryptamine-induced Ca2+-independent cGMP formation is mediated by nitric oxide in a nitric oxide synthase-independent manner in NG108-15 cells
    Arima, T
    Mizuno, T
    Ohshima, Y
    Kitamura, Y
    Segawa, T
    Nomura, Y
    NEUROSCIENCE RESEARCH, 1997, 27 (03) : 229 - 233
  • [39] ON THE ROLE OF NITRIC-OXIDE AS A CELLULAR MESSENGER IN BRAIN
    COLLARD, KJ
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 1995, 149 : 249 - 256
  • [40] Nitric oxide/cGMP signaling in the corpora allata of female grasshoppers
    Wirmer, Andrea
    Heinrich, Ralf
    JOURNAL OF INSECT PHYSIOLOGY, 2011, 57 (01) : 94 - 107