4.5 Review

Roles of Peroxisome Proliferator-Activated Receptor Gamma on Brain and Peripheral Inflammation

Journal

CELLULAR AND MOLECULAR NEUROBIOLOGY
Volume 38, Issue 1, Pages 121-132

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10571-017-0554-5

Keywords

Brain injury; Angiogenesis; Agonist; PPAR gamma; Inflammation; Angiotensin receptor blockers

Funding

  1. National Institute for Neurological Disorders and Stroke (NINDS) [R03NS095038]
  2. Department of Neuroscience at Georgetown University Medical Center
  3. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R03NS095038] Funding Source: NIH RePORTER

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Peroxisome proliferator-activated receptor gamma (PPAR gamma) has been implicated in the pathology of numerous diseases involving diabetes, stroke, cancer, or obesity. It is expressed in diverse cell types, including vessels, immune and glial cells, and neurons. PPAR gamma plays crucial roles in the regulation of cellular differentiation, lipid metabolism, or glucose homeostasis. PPAR gamma ligands also exert effects on attenuating degenerative processes in the brain, as well as in peripheral systems, and it has been associated with the control of anti-inflammatory mechanisms, oxidative stress, neuronal death, neurogenesis, differentiation, and angiogenesis. This review will highlight key advances in the understanding of the PPAR gamma-related mechanisms responsible for neuroprotection after brain injuries, both ischemia and traumatic brain injury, and it will also cover the natural and synthetic agonist for PPAR gamma, angiotensin receptor blockers, and PPAR gamma antagonists, used in experimental and clinical research. A better understanding of the pleiotropic mechanisms and applications of these drugs to improve the recovery and to repair the acute and chronic induced neuroinflammation after brain injuries will pave the way for more effective therapeutic strategies after brain deficits.

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