Agomelatine appears to be safe and efficacious in treating depressive symptoms in patients with schizophrenia. The risk of pharmacokinetic interactions with antipsychotic agents warrants the need of therapeutic drug monitoring, and regular recording of vital signs seems necessary. Further randomized trials will have to confirm these findings.
Despite statistically significant, cognitive improvements after 12 weeks of AGO treatment were clinically irrelevant. Our findings may be limited by baseline properties of the study sample and the study design. In particular, lacking a control group, it cannot be ruled out that improvements were unrelated to AGO treatment. That is why randomized controlled trials are needed to validate the relevance of AGO as a cognitive enhancer in schizophrenia.
Telomeres are nucleoprotein structures at the ends of linear chromosomes. In humans, they consist of TTAGGG repeats, which are bound by dedicated proteins such as the shelterin complex. This complex blocks unwanted DNA damage repair at telomeres, e.g. by suppressing non-homologous end joining (NHEJ) through its subunit TRF2. We here describe ZNF524, a zinc finger protein that directly binds telomeric repeats with nanomolar affinity and reveal the base-specific sequence recognition by co-crystallization with telomeric DNA. ZNF524 localizes to telomeres and specifically maintains the presence of the TRF2/RAP1 subcomplex at telomeres without affecting other shelterin members. Loss of ZNF524 concomitantly results in an increase in DNA damage signaling and recombination events. Overall, ZNF524 is a direct telomere-binding protein involved in the maintenance of telomere integrity.
Polymeric carbon nitrides (PCN) are sustainable, tunable, non-toxic and chemically stable materials that represent highly promising heterogeneous photocatalysts for light-driven hydrogen peroxide production via selective reduction of dioxygen. However, most of the studies on photocatalytic H2O2 production using PCN-based photocatalysts reported so far have used PCN powder suspensions and have been carried out in the presence of additional (sacrificial) electron donors, such as aliphatic or aromatic alcohols. Herein, we report the first multicomponent hybrid photocathode based on PCN that is capable of selective reduction of dioxygen to H2O2 under visible light irradiation (420 nm LED). A comparative analysis of various photocathode architectures is carried out using electronic absorption spectroscopy, surface photovoltage spectroscopy, open-circuit photopotential spectroscopy, and photocurrent measurements, including in-situ detection of formed H2O2 using microelectrodes. Notably, the ability of PCN-based photocathodes to catalyze the light-driven reduction of O2 to H2O2 in the absence of any additional electron donor is unambiguously demonstrated. Our study thus highlights the intrinsic nature of the photocatalytic activity of PCN in H2O2 production, and paves the way for the development of further PCN-based photocathodes in which PCN could be coupled with more effective light absorbers to increase the overall performance.
Polymeric carbon nitrides (PCN) are sustainable, tunable, non-toxic and chemically stable materials that represent highly promising heterogeneous photocatalysts for light-driven hydrogen peroxide production via selective reduction of dioxygen. However, most of the studies on photocatalytic H2O2 production using PCN-based photocatalysts reported so far have used PCN powder suspensions and have been carried out in the presence of additional (sacrificial) electron donors, such as aliphatic or aromatic alcohols. Herein, we report the first multicomponent hybrid photocathode based on PCN that is capable of selective reduction of dioxygen to H2O2 under visible light irradiation (420 nm LED). A comparative analysis of various photocathode architectures is carried out using electronic absorption spectroscopy, surface photovoltage spectroscopy, open-circuit photopotential spectroscopy, and photocurrent measurements, including in-situ detection of formed H2O2 using microelectrodes. Notably, the ability of PCN-based photocathodes to catalyze the light-driven reduction of O2 to H2O2 in the absence of any additional electron donor is unambiguously demonstrated. Our study thus highlights the intrinsic nature of the photocatalytic activity of PCN in H2O2 production, and paves the way for the development of further PCN-based photocathodes in which PCN could be coupled with more effective light absorbers to increase the overall performance.
Agomelatine efficacy appears to be independent of dosage and smoking status, pointing toward mechanisms beyond mere dose-response relationships. Further research will be necessary to validate these findings.
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