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High-dose perfluorooctanoic acid (PFOA) impairs oocyte maturation and offspring quality. However, the physiological concentrations of PFOA in follicular fluids of patients with premature ovarian insufficiency (POI) were detected at lower levels, thus the relationship between physiological PFOA and reproductive disorders remains elusive. Here, we investigated whether physiological PFOA exposure affects gonad function in adult zebrafish. Physiological PFOA exposure resulted in POI-like phenotypes in adult females, which exhibited decreased spawning frequency, reduced number of ovulated eggs, abnormal gonadal index, and aberrant embryonic mortality. Meanwhile, oocytes from PFOA-exposed zebrafish showed mitochondrial disintegration and diminished mitochondrial membrane potential. Unlike the high-dose treated oocytes exhibiting high reactive oxygen species (ROS) levels and excessive apoptosis, physiological PFOA reduced the ROS levels and did not trigger apoptosis. Interestingly, physiological PFOA exposure would not affect testis function, indicating specific toxicity in females. Mechanistically, PFOA suppressed the NAD+ biosynthesis and impaired mitochondrial function in oocytes, thus disrupting oocyte maturation and ovarian fertility. Nicotinamide mononucleotide (NMN), a precursor for NAD+ biosynthesis, alleviated the PFOA-induced toxic effects in oocytes and improved the oocyte maturation and fertility upon PFOA exposure. Our findings discover new insights into PFOA-induced reproductive toxicity and provide NMN as a potential drug for POI therapy. [ABSTRACT FROM AUTHOR]

A carbazole-based artificial light-harvesting system (LHS) was successfully fabricated based on the supramolecular assembly of AIE-enhanced donor (CTD), water-soluble phosphate-pillar[5]arene (WPP5), and eosin Y (ESY) acceptor. The formed WPP5-CTD possessed remarkable AIE emission, featuring an ideal energy donor for light harvesting. After encapsulation of ESY, the energy of WPP5-CTD was efficiently transferred to ESY in WPP5-CTD-ESY, and the antenna effect was 38.5, which was much higher than that of recently reported LHSs. Notably, WPP5-CTD-ESY was successfully utilized as a photocatalyst to realize the cross-coupling dehydrogenation reaction of diphenylphosphine oxide and benzothiazole derivatives, suggesting great potential for aqueous photocatalytic applications of this LHS. [ABSTRACT FROM AUTHOR]

The measurement of hemoglobin is a vital index for diagnosing and monitoring diseases in clinical practice. At present, solutions need to be found for the soreness, high risk of infection, and inconvenient operation associated with invasive detection methods. This paper proposes a method for non-invasively detecting hemoglobin levels based on multi-wavelength photoplethysmography (PPG) signals. AFE4490 and TMUX1109 were used to implement the low-cost collection of an eight-LED transmissive PPG signal. We used seven regular LEDs and one broadband LED (Osram SFH4737) as light sources. Additionally, a finger clip integrating multiple sensors was designed and manufactured via 3D printing to simultaneously monitor the LED–sensor distance and the pressure from the tester's finger during PPG signal acquisition. We used a method to extract features from PPG signals using a sliding-window's variance and an evaluation metric for PPG signals based on the AdaCost classification. Data were gathered from 56 participants from the Nephrology department, including 16 anemic patients. Pearson correlation analysis was conducted on the collected data to remove any data with a weak correlation. The advantage of using a broadband LED as a light source was also demonstrated. Several non-invasive hemoglobin regression models were created by applying AdaBoost, BPNN, and Random Forest models. The study's results indicate that the AdaBoost model produced the best performance, with a mean absolute error (MAE) of 2.67 g/L and a correlation coefficient (R2) of 0.91 The study results show that the device we designed and manufactured can achieve effective non-invasive hemoglobin detection and represents a new methodological approach to obtaining measurements that can be applied in a clinical setting. [ABSTRACT FROM AUTHOR]

Because cotton is the most important fiber crop, the differentiation and development mechanism of cotton fiber cells has been a hot topic in cotton research. NAC (for NAM, ATAF, and CUC2) is a class of plant‐specific transcription factor families that regulate multiple aspects of plant growth and development. Previously, we identified 33 differentially expressed NAC genes in upland cotton based on fiber‐related transcriptome profiling. In this study, we conducted chromosome localization, systematic evolution, and gene structural analysis of 242 NAC genes genome‐wide based on a high‐quality reference genome of upland cotton. In addition, the expression pattern analysis of 16 differentially expressed GhNACs was carried out by RT–PCR using ovules at early fiber initiation stages of n2 recessive naked seed mutant (n2NSM) and Xuzhou142 fuzzless–lintless mutant (Xu142fl). The results showed that GhNAC230 and GhNAC115 were most closely related to AtSND1 and downregulated in ovules of Xu142fl compared with n2NSM. Quantitative RT–PCR (qRT–PCR) analysis of GhNAC230 demonstrated its gradual accumulation from −1 days postanthesis (DPA) to 1 DPA in n2NSM and further confirmed its downregulated expression in 1 DPA ovules of Xu142fl compared to n2NSM. The current study predicted a pair of NAC genes that might be key candidate genes that are crucial for lint fiber development. [ABSTRACT FROM AUTHOR]