Literature DB >> 17981619

NAD+ and NADH in ischemic brain injury.

Weihai Ying1.   

Abstract

NAD+ and NADH have been emerging as the common mediators of energy metabolism, mitochondrial functions, calcium homeostasis, aging and cell death. NAD+ and NADH can affect cell death by various mechanisms, such as influencing energy metabolism, mitochondrial permeability transition pores, and apoptosis-inducing factor. Because energy failure, calcium disregulation and cell death are the key components in the tissue damaging cascade initiated by cerebral ischemia, it is likely that NAD+ and NADH play significant roles in ischemic brain damage. Many studies, including the findings that poly(ADP-ribose) polymerase-1 mediates ischemic brain injury and that NAD+ administration can decrease ischemic brain damage, have suggested significant roles of NAD+ and NADH in the debilitating illness. However, there is still distinct insufficiency of the information regarding the roles of NAD+ and NADH in ischemic brain injury. Because increasing evidence has indicated critical functions of NAD+ and NADH in various biological processes, future studies on the roles of NAD+ and NADH in cerebral ischemia may expose essential mechanisms underlying ischemic brain injury and suggest novel therapeutic strategies for the illness.

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Year:  2008        PMID: 17981619     DOI: 10.2741/2751

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  8 in total

Review 1.  Oxidative stress and NAD+ in ischemic brain injury: current advances and future perspectives.

Authors:  W Ying; Z-G Xiong
Journal:  Curr Med Chem       Date:  2010       Impact factor: 4.530

2.  MCU-dependent mitochondrial Ca2+ inhibits NAD+/SIRT3/SOD2 pathway to promote ROS production and metastasis of HCC cells.

Authors:  T Ren; H Zhang; J Wang; J Zhu; M Jin; Y Wu; X Guo; L Ji; Q Huang; H Zhang; H Yang; J Xing
Journal:  Oncogene       Date:  2017-06-26       Impact factor: 9.867

Review 3.  Postischemic oxidative stress promotes mitochondrial metabolic failure in neurons and astrocytes.

Authors:  Gary Fiskum; Camelia A Danilov; Zara Mehrabian; Linda L Bambrick; Tibor Kristian; Mary C McKenna; Irene Hopkins; E M Richards; Robert E Rosenthal
Journal:  Ann N Y Acad Sci       Date:  2008-12       Impact factor: 5.691

Review 4.  Mitochondrial mechanisms of cell death and neuroprotection in pediatric ischemic and traumatic brain injury.

Authors:  Courtney L Robertson; Susanna Scafidi; Mary C McKenna; Gary Fiskum
Journal:  Exp Neurol       Date:  2009-05-07       Impact factor: 5.330

5.  Protein kinase C epsilon regulates mitochondrial pools of Nampt and NAD following resveratrol and ischemic preconditioning in the rat cortex.

Authors:  Kahlilia C Morris-Blanco; Charles H Cohan; Jake T Neumann; Thomas J Sick; Miguel A Perez-Pinzon
Journal:  J Cereb Blood Flow Metab       Date:  2014-03-26       Impact factor: 6.200

6.  Visualization and quantification of NAD(H) in brain sections by a novel histo-enzymatic nitrotetrazolium blue staining technique.

Authors:  Irina S Balan; Gary Fiskum; Tibor Kristian
Journal:  Brain Res       Date:  2009-12-28       Impact factor: 3.252

Review 7.  Aspects of Tryptophan and Nicotinamide Adenine Dinucleotide in Immunity: A New Twist in an Old Tale.

Authors:  Hector Rodriguez Cetina Biefer; Anju Vasudevan; Abdallah Elkhal
Journal:  Int J Tryptophan Res       Date:  2017-06-14

Review 8.  Effects of ischemic preconditioning on mitochondrial and metabolic neruoprotection: 5' adenosine monophosphate-activated protein kinase and sirtuins.

Authors:  Charles W Jackson; Iris Escobar; Jing Xu; Miguel A Perez-Pinzon
Journal:  Brain Circ       Date:  2018-06-29
  8 in total

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