In order to explore the pollution characteristics of perfluorinated compounds (PFCs), 10 surface seawaters and 7 surface sediments were collected in offshore marine area of Shenzhen (offshore distance >2 km) in September 2013. All the samples were prepared by solid-phase extraction and analyzed using high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/ MS). The results showed that 10 PFCs, including C4, C6 and C8 perfluorinated sulfonates (PFSAs) and C5-C11, perfluorinated carboxylic acids (PFCAs) were detected in the surface waters. ∑ PFC concentrations ranged from 1.74 ng x L(-1) to 14.7 ng x L(-1) with PFBS, PFOS and PFOA being the dominant compounds. The spatial distribution of ∑ PFC concentrations displayed the characteristic of "the west being higher than the east", with ∑ PFC concentrations of Lingding Sea and Shenzhen Bay being higher than those of Daya Bay and Dapeng Bay (P < 0.05). The farther the sampling location was from the shore, the lower the ∑ PFC concentrations were. Direct sewage emissions and rivers emptying into the sea might be the primary sources of PFCs in the surface seawaters. 8 PFCs, including C6 and C8 PFSAs and C5, C6, and C8-C11 PFCAs were detected in the surface sediments. ∑ PFC concentrations ranged from 2.22 micorg x kg(-1) to 2.62 microg x kg(-1) with PFOS being the dominant compounds. There was a small change of ∑ PFC concentrations in surface sediments, which might be contributed by the adsorption from overlying water. The adsorption of PFCs on sediment significantly increased with the increasing length of carbon chain, and the adsorption of PFSA was higher than that of PFCA with the same length of carbon chain as PFSA. Additionally, the comparison with other seawater PFC measurements showed high PFBS pollution in this study, whereas the level of PFOS in sediment was close to those of other studies.
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Nutrients
June 2024
Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, Seoul 02447, Republic of Korea.
Astrocyte dysfunction and inflammation play a pivotal role in depression. In this study, we evaluated the antidepressant properties of root extract (HME), which is traditionally used for inflammation-related diseases, in a mouse model with astrocyte depletion that resembles the prefrontal cortex pathology of depressive patients. Mice were divided into four groups, with 10 mice per group.
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February 2024
Department of Neurology, BG University Hospital Bergmannsheil, Ruhr-University Bochum, Bochum, Germany.
Introduction: Renewal of extinguished responses is associated with higher activity in specific extinction-relevant brain regions, i.e., hippocampus (HC), inferior frontal gyrus (IFG), and ventromedial PFC (vmPFC).
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October 2021
Experimental Cardiovascular Imaging, Heinrich-Heine-University, Düsseldorf, Germany.
The pathophysiology of the initiation and progression of abdominal aortic aneurysms (AAAs) and aortic dissections (AADs) is still unclear. However, there is strong evidence that monocytes and macrophages are of crucial importance in these processes. Here, we utilized a molecular imaging approach based on background-free F MRI and employed perfluorocarbon nanoemulsions (PFCs) for F labeling of monocytes/macrophages to monitor vascular inflammation and AAA/AAD formation in angiotensin II (angII)-treated apolipoproteinE-deficient (apoE) mice.
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July 2020
College of Korean Medicine, Kyung Hee University, Seoul, Republic of Korea.
Cell Chem Biol
March 2020
H3 Biomedicine Inc., 300 Technology Square, Cambridge, MA 02139, USA. Electronic address:
Carbamoyl phosphate synthetase 1 (CPS1) catalyzes the first step in the ammonia-detoxifying urea cycle, converting ammonia to carbamoyl phosphate under physiologic conditions. In cancer, CPS1 overexpression supports pyrimidine synthesis to promote tumor growth in some cancer types, while in others CPS1 activity prevents the buildup of toxic levels of intratumoral ammonia to allow for sustained tumor growth. Targeted CPS1 inhibitors may, therefore, provide a therapeutic benefit for cancer patients with tumors overexpressing CPS1.
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