4.7 Article

Overexpression of PDE4D in mouse liver is sufficient to trigger NAFLD and hypertension in a CD36-TGF-131 pathway: therapeutic role of roflumilast

Journal

PHARMACOLOGICAL RESEARCH
Volume 175, Issue -, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2021.106004

Keywords

PDE4D; Nonalcoholic fatty liver; Hypertension; CD36; TGF-beta 1

Funding

  1. National Natural Science Foundation ofChina [81773730, 81729004, 82070406, U1601227]
  2. Department of Science and Technology of Guangdong [2015B020225006, 2020A1515011158]
  3. Department of Edu-cation of Guangdong [2020KTSCX106]

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Recent studies have shown that PDE4-cAMP signaling is relevant to metabolic disorders. PDE4 plays a crucial role in the pathogenesis of NAFLD and associated hypertension, with PDE4 inhibitor roflumilast having the potential for future use in prevention or treatment of these conditions.
Emerging evidence has shown that nonalcoholic fatty liver disease (NAFLD) may be both a consequence and a cause of hypertension. Recent studies have demonstrated that phosphodiesterase 4 (PDE4)-cAMP signaling represents a pathway relevant to the pathophysiology of metabolic disorders. This study aims to investigate the impact and the underlying mechanism of PDE4 in the pathogenesis of NAFLD and its associated hypertension. Here we demonstrated that high-fat-diet (HFD) fed mice developed NAFLD and hypertension, with an associated increase in hepatic PDE4D expression, which can be prevented and even reversed by PDE4 inhibitor roflumilast. Furthermore, we demonstrated that hepatic overexpression of PDE4D drove significant hepatic steatosis and elevation of blood pressure. Mechanistically, PDE4D activated fatty acid translocase CD36 signaling which facilitates hepatic lipid deposition, resulting in TGF-beta 1 production by hepatocytes and excessive TGF-beta 1 signaling in vessels and consequent hypertension. Specific silencing of TGF-beta 1 in hepatocytes by siRNA using poly (beta-amino ester) nanoparticles significantly normalized hepatic PDE4D overexpression-activated TGF-beta 1 signaling in vessels and hypertension. Together, the conclusions indicated that PDE4D plays an important role in the pathogenesis of NAFLD and associated hypertension via activation of CD36-TGF-beta 1 signaling in the liver. PDE4 inhibitor such as roflumilast, which is clinically approved for chronic obstructive pulmonary disease (COPD) treatment, has the potential to be used as a preventive or therapeutic drug against NAFLD and associated hypertension in the future.

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