4.4 Article

Arginine is neuroprotective through suppressing HIF-1α/LDHA-mediated inflammatory response after cerebral ischemia/reperfusion injury

Journal

MOLECULAR BRAIN
Volume 13, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13041-020-00601-9

Keywords

Arginine; Neuroinflammation; Ischemia stroke; LDHA; HIF-1 alpha; Neuroprotection

Categories

Funding

  1. National Key Basic Research Program of China [2014CB541606]
  2. National Key R&D Program of China [2018YFC1312300, 2019YFC010167]
  3. National Natural Science Foundation of China (NSFC) [81470599]
  4. Key Research and Development Project of Shandong [2019JZZY021010]
  5. Fund of Collaborative Innovation Center for Brain Science
  6. Natural Science Foundation of China (NSFC) [81701291]

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Neuroinflammation is a secondary response following ischemia stroke. Arginine is a non-essential amino acid that has been shown to inhibit acute inflammatory reaction. In this study we show that arginine treatment decreases neuronal death after rat cerebral ischemia/reperfusion (I/R) injury and improves functional recovery of stroke animals. We also show that arginine suppresses inflammatory response in the ischemic brain tissue and in the cultured microglia after OGD insult. We further provide evidence that the levels of HIF-1 alpha and LDHA are increased after rat I/R injury and that arginine treatment prevents the elevation of HIF-1 alpha and LDHA after I/R injury. Arginine inhibits inflammatory response through suppression of HIF-1 alpha and LDHA in the rat ischemic brain tissue and in the cultured microglia following OGD insult, and protects against ischemic neuron death after rat I/R injury by attenuating HIF-1 alpha/LDHA-mediated inflammatory response. Together, these results indicate a possibility that arginine-induced neuroprotective effect may be through the suppression of HIF-1 alpha/LDHA-mediated inflammatory response in microglia after cerebral ischemia injury.

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