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1.
Environ Anal Health Toxicol ; 39(2): e2024017-0, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-39054831

RESUMO

Microplastic pollution has become a global menace, and water, being a major "sink" for pollutants, represents a significant source of human exposure. This study aimed to assess the safety of borehole water in Birnin Kebbi, Nigeria, specifically concerning microplastic pollution. Water samples were collected from boreholes in selected areas, including Bayan Kara, Malali, Rafin Atiku, Aliero Quarters, GwadanGaji, FUBK Takeoff Site, Kalgo Market, and Tarasa. Microplastics were extracted from the water samples through filtration using glass fiber filter papers, and were subsequently subjected to spectroscopy and microscopy to determine concentrations, shapes, and polymer types. Health risks associated with the microplastics were also calculated. The results revealed that the samples from Tarasa exhibited the highest concentrations of microplastics (96.967 particles/L), followed by Bayan Kara (92.70 particles/L), Rafin Atiku (92.33 particles/L), GwadanGwaji (92.30 particles/L), FUBK Takeoff Site (91.07 particles/L), Aliero Quarters (90.43 particles/L), Kalgo Market (88.00 particles/L), and Malali (86.40 particles/L). The most dominant shape was fibers (73 %), followed by fragments (16 %), foams (6 %), and filaments (5 %). Polyethylene and polyamide, in that order, were the most dominant polymers, while polystyrene was the least common. The majority of risk scores were classified as III. It can be inferred from the results that microplastic pollution in borehole water poses a health hazard in the city. Consumers of borehole water in the studied areas are advised to treat the water before consumption to mitigate potential health risks.

2.
Environ Anal Health Toxicol ; 39(2): e2024021-0, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-39054835

RESUMO

The global occurrence of microplastics and their poorly understood health implications underscore the need for scientific investigation. This study aimed to assess the effects of microplastics exposure. Twenty-five (25) albino rats (Rattus norvegicus) were divided into five (5) groups, each consisting of five rats. Group 1 (the negative control) received normal feed; group 2 (the positive control) was administered a 10 % lead acetate solution; and groups 3, 4, and 5 were administered 1 %, 5 %, and 10 % microplastic solutions, respectively. The rats were monitored for 28 days, after which blood samples were taken for hematological and lipid profiles as well as liver and kidney function parameters. The results revealed dose-dependent significant (p < 0.05) alterations in the health indices of the treated rats and the positive control compared with the negative control. Specifically, the hematological parameters, including the white blood cells (WBC) and its subtypes, were reduced, indicating immunosuppressive effects, and the red blood cells (RBC), hemoglobin (HGB), hematocrit (HCT), platelets, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), and mean corpuscular hemoglobin concentration (MCHC) were reduced, indicating anemia. The 1 % and 5 % microplastic solutions raised the lipid profiles of the treated rats, including total cholesterol (TC), triglycerides (TG), high-density lipoprotein (HDL), and low-density lipoprotein (LDL), while the 10 % concentration decreased them, causing hyperlipidemia and hypolipidemia, respectively. The liver function parameters, including total protein (TP), albumin (ALB), aspartate transaminase (AST), alanine transaminase (ALT), and alkaline phosphatase (ALP), were elevated, indicating liver damage. Elevation of kidney function parameters, including sodium ion (Na+), potassium ion (K+), chloride ion (Cl-), urea, and creatinine (CRT), were noticed, suggesting kidney injuries. It can be inferred from these results that microplastics are toxic. Hence, human exposure to microplastics should be reduced to a minimum.

3.
Curr Probl Cardiol ; 49(1 Pt B): 102072, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37689374

RESUMO

Premature ventricular contractions (PVC) are a type of ventricular arrhythmias, occurring as a result of formation or reentry of an abnormal impulse in the ventricular myocardium or in the Purkinje system. PVC occurs commonly in healthy individuals and is observed in 1%-4% of the population. Several lifestyle factors like stress levels, caffeine, drugs, alcohol, nicotine, sleep, and physical exercise have been implicated in increasing the risk. Caffeine and drugs precipitate heightened cardiac stimulation, precipitating PVCs. Excessive alcohol and nicotine disturb the electrical pathways resulting in PVCs. Higher rates of PVCs have been associated with obesity. Individuals with insomnia and increased stress levels are also at an increased risk due to an imbalance in the autonomic system. Exercise is known to induce PVCs, including in healthy, asymptomatic individuals. Modification of these factors can decrease PVC risk. This article aims to provide a comprehensive review of the effects of lifestyle factors on PVC.


Assuntos
Cafeína , Complexos Ventriculares Prematuros , Humanos , Nicotina , Ventrículos do Coração , Complexos Ventriculares Prematuros/etiologia , Complexos Ventriculares Prematuros/complicações , Estilo de Vida
4.
SAGE Open Med Case Rep ; 11: 2050313X231180747, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37440972

RESUMO

Nicolau syndrome is a rare condition characterized by severe pain at the site of injection, leading to ulceration and necrosis of the local tissues. Its presentation is usually acute. Nicolau syndrome is commonly seen in patients after intramuscular, intra-articular, or subcutaneous injections of non-steroidal anti-inflammatory drugs, antiepileptics, antipsychotics, antibiotics, antihistamines, and corticosteroids. Immediate diagnosis and management of this syndrome are of great importance. We herein report a rare presentation of Nicolau syndrome in a 36-year-old married male who suffered from paranoid schizophrenia for the past 3 years. The patient presented with dull pain, mild swelling, and necrotic ulceration over the injection site after receiving intramuscular fluphenazine. The patient underwent wound debridement and was given prophylactic antibiotics. Despite a wide range of therapeutic options for the management of Nicolau syndrome described in the literature, there exist limited guidelines for its management.

5.
Cells ; 12(3)2023 01 17.
Artigo em Inglês | MEDLINE | ID: mdl-36766690

RESUMO

(1) Background: Apolipoprotein E (ApoE) is a critical plasma apolipoprotein for lipid transport and nonlipid-related functions. Humans possess three isoforms of ApoE (2, 3, and 4). ApoE2, which exhibits beneficial effects on cardiac health, has not been adequately studied. (2) Methods: We investigated the cardiac phenotypes of the humanized ApoE knock-in (hApoE KI) rats and compared to wild-type (WT) and ApoE knock-out (ApoE KO) rats using echocardiography, ultrasound, blood pressure measurements, histology strategies, cell culture, Seahorse XF, cardiomyocyte contractility and intracellular Ca2+ tests, and Western blotting; (3) Results: hApoE2 rats exhibited enhanced heart contractile function without signs of detrimental remodeling. Isolated adult hApoE2 cardiomyocytes had faster and stronger sarcomere contractility because of more mitochondrial energy generation and stimulation-induced fast and elevated intracellular Ca2+ transient. The abundant energy is a result of elevated mitochondrial function via fatty acid ß-oxidation. The fast and elevated Ca2+ transient is associated with decreased sarcoplasmic reticulum (SR) Ca2+ ATPase (SERCA2) and increased expression of cardiac ryanodine receptor 2 (RyR2) conducting a potent Ca2+ release from SR.; (4) Conclusions: Our studies validated the association of polymorphic ApoEs with cardiac health in the rat model, and revealed the possible mechanisms of the protective effect of ApoE2 against heart diseases.


Assuntos
Miócitos Cardíacos , Retículo Sarcoplasmático , Ratos , Humanos , Animais , Miócitos Cardíacos/metabolismo , Apolipoproteína E2/metabolismo , Apolipoproteína E2/farmacologia , Retículo Sarcoplasmático/metabolismo , Ecocardiografia
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