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There is an increasing tendency to replace conventional agricultural plastic mulching films with biodegradable alternatives. However, while the latter biodegrade well under controlled conditions (e.g. industrial compost), their biodegradation in non-target environments (e.g. aquatic environments) is questioned and poorly understood. Therefore, in this study, microplastics derived from conventional polyethylene (PE) and biodegradable polybutylene adipate terephthalate starch blend (PBAT) mulching films were exposed to UV irradiation and subsequently tested for their ready biodegradability in an aqueous medium where changes in their characteristics were evaluated. The results showed limited biodegradation for pristine and UV-aged PE: no morphological, surface chemical or internal changes were observed. Pristine PBAT showed signs of initial biodegradation, while UV-aged PBAT biodegraded by up to 57%. New functional groups appeared on the PBAT surface after UV irradiation according to FTIR analysis and crystallinity increased after biodegradation. Elemental analysis revealed a range of metals in PE and PBAT microplastics. No changes in metal distribution analysed in microplastic after UV-aging or biodegradation were found, except that less titanium was present in PBAT after biodegradation indicating potential leaching. None of the PBAT microplastics had ecotoxic effects towards the aquatic plant Lemna minor. Pristine and UV-aged PE showed negative effects on roots, but these were not observed after biodegradation. Low biodegradation of pristine PBAT and possible leaching of metals demonstrated here raise questions about the sustainable use of biodegradable alternatives, especially when they enter non-target environments.
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http://dx.doi.org/10.1016/j.envpol.2025.126408 | DOI Listing |
J Cereb Blood Flow Metab
September 2025
Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.
Preclinical PET studies offer the opportunity to elucidate molecular mechanisms underlying early neurodevelopment with minimal invasiveness. We demonstrated the feasibility of fetal brain PET in four pregnant rats ( = 42 fetuses). [F]FDG uptake in rat fetuses was readily visualized by PET imaging.
View Article and Find Full Text PDFJ Cereb Blood Flow Metab
September 2025
Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria.
Functional PET (fPET) identifies stimulation-specific changes of physiological processes, individual molecular connectivity and group-level molecular covariance. Since there is currently no consistent analysis approach available for these techniques, we present a toolbox for unified fPET assessment. The toolbox supports analysis of data obtained with a variety of radiotracers, scanners, experimental protocols, cognitive tasks and species.
View Article and Find Full Text PDFCell Physiol Biochem
September 2025
Department of Histology and Embryology and Vascular Biology Student Research Club, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University in Torun, 85-092 Bydgoszcz, Poland, E-Mail:
Migrasomes are newly discovered, migration-dependent organelles that mediate the release of cellular contents into the extracellular environment through a process known as migracytosis. Since their identification in 2014, growing evidence has highlighted their critical roles in intercellular communication, organ development, mitochondrial quality control, and disease pathogenesis. Migrasome biogenesis is a complex, multi-step process tightly regulated by lipid composition, tetraspanin-enriched microdomains, and molecular pathways involving sphingomyelin synthase 2, Rab35, and integrins.
View Article and Find Full Text PDFMacrophage Migration Inhibitory Factor (MIF) is a pleiotropic cytokine that acts as a central regulator of inflammation and immune responses across diverse organ systems. Functioning upstream in immune activation cascades, MIF influences macrophage polarization, T and B cell differentiation, and cytokine expression through CD74, CXCR2/4/7, and downstream signaling via NF-κB, ERK1/2, and PI3K/AKT pathways. This review provides a comprehensive analysis of MIF's mechanistic functions under both physiological and pathological conditions, highlighting its dual role as a protective mediator during acute stress and as a pro-inflammatory amplifier in chronic disease.
View Article and Find Full Text PDFCell Physiol Biochem
September 2025
Department of General Practice, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China, E-Mail:
Background/aims: Ubiquitin D (UBD), a member of the ubiquitin-like modifier (UBL) family, is significantly overexpressed in various cancers and is positively correlated with tumor progression. However, the role and underlying mechanisms of UBD in rheumatoid arthritis (RA) remain poorly understood. This study aimed to investigate the effects of UBD knockdown on the progression of RA.
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