2020
DOI: 10.1016/j.arr.2020.101186
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Protective response of Sestrin under stressful conditions in aging

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Cited by 16 publications
(26 citation statements)
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“…Meanwhile, they found no significant correlations between serum sestrin2 levels and BMI as well as SBP, DBP, total cholesterol, LDL‐C, HDL‐C, FBS, and HbA1c in individuals with normal glucose tolerance 45 . A possible explanation for this paradoxical increase in serum sestrin2 in subjects with metabolic syndrome might be a compensatory mechanism to overcome the metabolic stress or resistance to sestrin2 41,45 . In the current study, we did not find any significant correlation between sestrin2 and anthropometric characteristics including BMI, indicating that the reduced level of sestrin2 may not be a consequence of obesity.…”
Section: Discussioncontrasting
confidence: 72%
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“…Meanwhile, they found no significant correlations between serum sestrin2 levels and BMI as well as SBP, DBP, total cholesterol, LDL‐C, HDL‐C, FBS, and HbA1c in individuals with normal glucose tolerance 45 . A possible explanation for this paradoxical increase in serum sestrin2 in subjects with metabolic syndrome might be a compensatory mechanism to overcome the metabolic stress or resistance to sestrin2 41,45 . In the current study, we did not find any significant correlation between sestrin2 and anthropometric characteristics including BMI, indicating that the reduced level of sestrin2 may not be a consequence of obesity.…”
Section: Discussioncontrasting
confidence: 72%
“…As mentioned before, we found that plasma levels of sestrin2 in patients with PCOS were significantly lower than those in the healthy controls. Interestingly, this finding contradicts some of the previous research on cardiovascular and pulmonary diseases, cancer, and neurodegenerative disorders which found an increase in the circulating sesrin2 levels in the patients 40,41 . It has been suggested that induction of sestrin2 in these diseases protects against damage associated with different stress conditions 41 .…”
Section: Discussionmentioning
confidence: 63%
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“…As a result, the number of damaged mitochondria increases, which in turn stimulates the accumulation of ROS, contributing to further cell damage [29,33,37]. Together, increased metabolic activity, impaired mitochondrial function, insufficient concentration of protective redox molecules (e.g., H 2 S), and inflammation prompt high spending of NAD+ and ROS accumulation [85,86,261]. These events of cellular aging further trigger advanced pathological processes, accumulation of senescent cells, and development of age-related disorders [262].…”
Section: Regeneration and Metabolic Disordersmentioning
confidence: 99%