2012
DOI: 10.1007/s11357-011-9365-7
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Age-related changes in nitric oxide activity, cyclic GMP, and TBARS levels in platelets and erythrocytes reflect the oxidative status in central nervous system

Abstract: Aging is associated with an increased susceptibility to neurodegenerative disorders which has been linked to chronic inflammation. This process generates oxygen-reactive species, ultimately responsible for a process known as oxidative stress, leading to changes in nitric oxide (NO), and cyclic guanosine monophosphate (cyclic GMP) signaling pathway. In previous studies, we showed that human aging was associated with an increase in NO Synthase (NOS) activity, a decrease in basal cyclic GMP levels in human platel… Show more

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Cited by 27 publications
(21 citation statements)
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References 49 publications
(53 reference statements)
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“…TBARS increased with age in erythrocytes [43] and were reported to be lower in females compared to males [44]. TBARS increased with increasing physical fitness [10].…”
Section: Reviewmentioning
confidence: 99%
“…TBARS increased with age in erythrocytes [43] and were reported to be lower in females compared to males [44]. TBARS increased with increasing physical fitness [10].…”
Section: Reviewmentioning
confidence: 99%
“…Phosphodiesterase 9A inhibition by 69 demonstrated an increase in basal synaptic transmission and enhanced LTP better in older rats compared to younger rats [197]. This is likely due to age-related decreases in cGMP levels [159,236] rather than changes in PDE9A expression levels, which have been shown to change during developmental stages [154], but do not significantly differ between young and old rats [237]. Additionally, expression of PDE9A in post-mortem brain tissue of patients with Alzheimer's disease shows the same distribution as in healthy brain tissues of comparable age [156].…”
Section: Clinical Trialsmentioning
confidence: 96%
“…Its unremarkable safety profile can be interpreted as demonstrating the safety of both 5HT 3 R antagonist and α7 nAChR partial agonist mechanistic approaches. The 236 A. Mazurov and D. Yohannes discovery that tropisetron is also a potent partial agonist for α7 nAChRs gives cause for the reexamination of both clinical and preclinical findings with this compound, particularly when it displayed pharmacological effects different from other 5HT 3 R antagonists. It was reported that the 5HT 3 R antagonists tropisetron and ondansetron had qualitatively different results in learning and memory paradigms in rats [172]; tropisetron, but not the selective 5-HT 3 R antagonist ondansetron, attenuated PCPinduced cognitive deficits in mice, and this effect of tropisetron was blocked by coadministration of the selective α7 nAChR antagonist MLA [173].…”
Section: α7 Nachr Agonists For Schizophreniamentioning
confidence: 99%
“…Phosphodiesterase 9A inhibition by 69 demonstrated an increase in basal synaptic transmission and enhanced LTP better in older rats compared to younger rats [197]. This is likely due to age-related decreases in cGMP levels [159,236] rather than changes in PDE9A expression levels, which have been shown to change during developmental stages [154], but do not significantly differ between young and old rats [237]. Additionally, expression of PDE9A in post-mortem brain tissue of patients with Alzheimer's disease shows the same distribution as in healthy brain tissues of comparable age [156].…”
Section: Summary Outlook Conclusionmentioning
confidence: 99%