2021
DOI: 10.1016/j.brainresbull.2021.03.016
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Sirtuins, a potential target in Traumatic Brain Injury and relevant experimental models

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Cited by 3 publications
(3 citation statements)
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“…Sirtuins (SIRTs) are ubiquitous regulators of cell activities that are class III histone deacetylases and have been shown to have neuroprotective properties in a variety of neurodegenerative disorders (Liu et al 2021;Ranadive et al 2021). In PVN, SIRT1 stimulates the HPA axis and basal glucocorticoid (GC) levels by increasing CRH production via an increase in prohormone convertase 2 (PC2) biosynthesis, which is required for the maturation of CRH from pro-CRH (Toorie et al 2016;Yamamoto and Takahashi 2018).…”
Section: Sirtuins and Ptsdmentioning
confidence: 99%
“…Sirtuins (SIRTs) are ubiquitous regulators of cell activities that are class III histone deacetylases and have been shown to have neuroprotective properties in a variety of neurodegenerative disorders (Liu et al 2021;Ranadive et al 2021). In PVN, SIRT1 stimulates the HPA axis and basal glucocorticoid (GC) levels by increasing CRH production via an increase in prohormone convertase 2 (PC2) biosynthesis, which is required for the maturation of CRH from pro-CRH (Toorie et al 2016;Yamamoto and Takahashi 2018).…”
Section: Sirtuins and Ptsdmentioning
confidence: 99%
“…Sirtuins, including SIRT1, are NAD+-dependent protein deacetylases, and have been shown to exhibit neuroprotective activities in animal models through reduction of neuroinflammation mediated by the NLRP3 inflammasome and cytokine/NF-κB (Ranadive et al, 2021). Whilst NAM exerts feedback inhibition to the sirtuin reactions, once administered to cells, NAM is converted to NAD+, resulting in a temporary initial inhibition of SIRT1, followed by an increase in the activity (Hwang and Song, 2017).…”
Section: Vitamin B3 (Nicotinamide)mentioning
confidence: 99%
“…In addition, the SIRT2 inhibitor AK-7 improves the outcome of brain ischemia independent of p38 activation in mice [ 100 ]. On the contrary, SIRT2 inhibition was reported to exacerbate traumatic brain injury [ 101 , 102 ]. AK-7 administration in mice treated with experimental traumatic brain injury increases the volume of brain edema lesion, neuroinflammation, and blood-brain barrier disruption via both increased K310 acetylation and nuclear translocation of NF-kappaB p65.…”
Section: Sirt2 Mirnas Hypoxia Oxidative Stress and Neurodegenerative Diseasesmentioning
confidence: 99%