2019
DOI: 10.1007/s10522-018-09794-y
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Therapeutic effects of curcumin on age-induced alterations in daily rhythms of clock genes and Sirt1 expression in the SCN of male Wistar rats

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Cited by 16 publications
(5 citation statements)
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“…Even more recently, it has been hypothesized that the antiaging effect of CUR may rely on the control of core clock genes on which Sirt1 belongs alongside rBmal1, rCry1, rCry2, rPer1, rPer2, and rRev-erba. CUR treatment in middle aged male Wistar rats restored the phase and daily pulse of rCry1, rCry2, rPer1, and rPer2 as in the young, whereas only rPer1 and partly rBmal1, rCry1, and rCry2 were restored in the old ones [164]. Moreover, it has been shown that CUR mitigated mouse ovarian aging, upgraded embryonic development, promoted oocyte maturation and fertilization via improvement of ovarian hormones, BioMed Research International and elevated the amounts of SIRT1 and 3 genes as well as attenuation of aging-associated oxidative stress and cell death [165].…”
Section: Studies Of Cell Senescence: Evidence From Mice Andmentioning
confidence: 86%
“…Even more recently, it has been hypothesized that the antiaging effect of CUR may rely on the control of core clock genes on which Sirt1 belongs alongside rBmal1, rCry1, rCry2, rPer1, rPer2, and rRev-erba. CUR treatment in middle aged male Wistar rats restored the phase and daily pulse of rCry1, rCry2, rPer1, and rPer2 as in the young, whereas only rPer1 and partly rBmal1, rCry1, and rCry2 were restored in the old ones [164]. Moreover, it has been shown that CUR mitigated mouse ovarian aging, upgraded embryonic development, promoted oocyte maturation and fertilization via improvement of ovarian hormones, BioMed Research International and elevated the amounts of SIRT1 and 3 genes as well as attenuation of aging-associated oxidative stress and cell death [165].…”
Section: Studies Of Cell Senescence: Evidence From Mice Andmentioning
confidence: 86%
“…Thus, the development of the metabolic syndrome may be significantly influenced by hypothalamic inflammation. It is worth mentioning that the interaction between SIRT1 and the hypothalamic clock genes (i.e., rBmal1, rPer1, rPer2, rCry1, rCry2 , and rRev-erbα ) decreases with age, which would lead to reduced dorsal medial hypothalamic (DMH) and lateral hypothalamic (LH) activity [ 27 , 28 ].…”
Section: Changes In Structure and Function In Endocrine Glands During...mentioning
confidence: 99%
“…With aging, the hypothalamus undergoes the following changes in aging: a significant reduction in blood supply [ 16 ]; the proliferation of connective tissue [ 17 ]; a change in cell morphology [ 18 ]; a reduction in the gonadotropin-releasing hormone (GnRH) [ 20 ], the growth hormone releasing hormone (GHRH) [ 20 ], the thyrotropin-releasing hormone (TRH) [ 20 ], and in the monoamine neurotransmitter levels [ 23 ]. Molecular mechanisms of aging include the following: a blocked TNF-α and IL-1β signaling; the loss of neural stem cells [ 24 ]; reduced autophagy [ 25 ]; enhanced mTOR activity [ 26 ]; and reduced SIRT1 expression in SCN, thereby resulting in reduced dorsal medial hypothalamic (DMH) and lateral hypothalamic (LH) activity [ 27 , 28 ].…”
Section: Figurementioning
confidence: 99%
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“…However, the concurrent administration of curcumin ameliorated these behavioural changes and modulated the expression of the Period Circadian Regulator 1 (PER1) gene [189]. In other animal studies, age-induced alterations in the daily rhythms of clock genes were restored by curcumin administration [190,191]. The PER1 gene and other clock genes are involved in biological processes such as feeding behaviour, sleep deprivation and vulnerability to depression [192][193][194][195].…”
Section: Clock Gene Expressionmentioning
confidence: 99%