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1.
Arch Toxicol ; 98(9): 2971-2984, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-38748041

RESUMEN

Cannabidivarin (CBDV) and cannabigerol (CBG) are minor phytocannabinoids from Cannabis sativa, whose health benefits have been reported. However, studies about the impact of these cannabinoids on fundamental cellular processes in placentation are scarce. Placental development involves physiological endoplasmic reticulum (ER) stress, however when exacerbated it can lead to altered angiogenesis and pregnancy disorders, such as intrauterine growth restriction and preeclampsia. In this work, the effects of CBDV and CBG (1-10 µM) on placental extravillous trophoblasts were studied, using the in vitro model HTR-8/SVneo cells. Both cannabinoids induced anti-proliferative effects and reactive oxygen/nitrogen species generation, which was dependent on transient receptor potential vanilloid 1 (TRPV1) activation. Moreover, CBDV and CBG significantly upregulated, in a TRPV-1 dependent manner, the gene expression of HSPA5/Glucose-regulated protein 78 (GRP78/BiP), a critical chaperone involved in ER stress and unfolded protein response (UPR) activation. Nevertheless, the UPR pathways were differentially activated. Both cannabinoids were able to recruit the IRE branch, while only CBDV enhanced the expression of downstream effectors of the PERK pathway, namely p-eIF2α, ATF4 and CHOP. It also augmented the activity of the apoptotic initiator caspases-8 and -9, though the effector caspases-3/-7 were not activated. TRB3 expression was increased by CBDV, which may hinder apoptosis termination. Moreover, both compounds upregulated the mRNA levels of the angiogenic factors VEGFA, PGF and sFLT1, and disrupted the endothelial-like behavior of HTR-8/SVneo cells, by reducing tube formation. Thus, CBDV and CBG treatment interferes with EVTs functions and may have a negative impact in placentation and in pregnancy outcome.


Asunto(s)
Cannabinoides , Chaperón BiP del Retículo Endoplásmico , Estrés del Retículo Endoplásmico , Canales Catiónicos TRPV , Trofoblastos , Respuesta de Proteína Desplegada , Humanos , Trofoblastos/efectos de los fármacos , Trofoblastos/metabolismo , Respuesta de Proteína Desplegada/efectos de los fármacos , Canales Catiónicos TRPV/metabolismo , Canales Catiónicos TRPV/genética , Línea Celular , Femenino , Embarazo , Estrés del Retículo Endoplásmico/efectos de los fármacos , Cannabinoides/farmacología , Proliferación Celular/efectos de los fármacos , Especies Reactivas de Oxígeno/metabolismo , Proteínas de Choque Térmico/metabolismo , Proteínas de Choque Térmico/genética , Placenta/efectos de los fármacos , Placenta/metabolismo , Neovascularización Fisiológica/efectos de los fármacos , Angiogénesis
2.
Nutrients ; 6(12): 5819-38, 2014 Dec 12.
Artículo en Inglés | MEDLINE | ID: mdl-25514562

RESUMEN

Astaxanthin (ASTA) is a pinkish-orange carotenoid commonly found in marine organisms, especially salmon. ASTA is a powerful antioxidant and suggested to provide benefits for human health, including the inhibition of LDL oxidation, UV-photoprotection, and prophylaxis of bacterial stomach ulcers. Exercise is associated to overproduction of free radicals in muscles and plasma, with pivotal participation of iron ions and glutathione (GSH). Thus, ASTA was studied here as an auxiliary supplement to improve antioxidant defenses in soleus muscles and plasma against oxidative damage induced by exhaustive exercise. Long-term 1 mg ASTA/kg body weight (BW) supplementation in Wistar rats (for 45 days) significantly delayed time to exhaustion by 29% in a swimming test. ASTA supplementation increased scavenging/iron-chelating capacities (TEAC/FRAP) and limited exercise-induced iron overload and its related pro-oxidant effects in plasma of exercising animals. On the other hand, ASTA induced significant mitochondrial Mn-dependent superoxide dismutase and cytosolic glutathione peroxidase antioxidant responses in soleus muscles that, in turn, increased GSH content during exercise, limited oxidative stress, and delayed exhaustion. We also provided significant discussion about a putative "mitochondrial-targeted" action of ASTA based on previous publications and on the positive results found in the highly mitochondrial populated (oxidative-type) soleus muscles here.


Asunto(s)
Antioxidantes/farmacología , Suplementos Dietéticos , Fatiga/sangre , Músculo Esquelético/efectos de los fármacos , Animales , Biomarcadores/sangre , Glucemia/metabolismo , Catalasa/metabolismo , Colesterol/sangre , Glutatión/sangre , Glutatión Peroxidasa/metabolismo , Hemoglobinas/metabolismo , Hierro/sangre , Masculino , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Músculo Esquelético/metabolismo , Oxidación-Reducción , Estrés Oxidativo/efectos de los fármacos , Condicionamiento Físico Animal , Ratas , Ratas Wistar , Superóxido Dismutasa/metabolismo , Triglicéridos/sangre , Ácido Úrico/sangre , Xantófilas/farmacología
3.
J Cancer Educ ; 23(1): 63-4, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18444049

RESUMEN

BACKGROUND: This is an update of a 10-years student-staffed oncology clinic. METHODS: Students are divided into 4 teams; each sees 1 to 2 outpatients weekly. RESULTS: By April 2006, 95 medical students participated, 89% for 2 or more years; 70% reported activity contributed to ability to read medical papers, and 59% improved their scientific writing. Of 39 students currently involved, 33 (84%) improved clinical skills in taking history, 27 (69%) in physical examination, and 34 (87%) in physician-patient relation. A total of 21 (56%) reported increased knowledge in general internal medicine. Although only 11% of former students pursued a specialty in Medical Oncology, 77% rated this clinic as the best extracurricular activity. CONCLUSIONS: Attendance of outpatient clinic in medical oncology can contribute significantly to the general medical education.


Asunto(s)
Educación de Pregrado en Medicina , Servicio de Oncología en Hospital , Servicio Ambulatorio en Hospital , Estudiantes de Medicina , Brasil , Humanos , Pacientes Ambulatorios , Factores de Tiempo , Recursos Humanos
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