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1.
Sci Rep ; 13(1): 2730, 2023 02 15.
Artigo em Inglês | MEDLINE | ID: mdl-36792695

RESUMO

Octopus vulgaris (Cuvier, 1797) is a cephalopod species with great economic value. In western Asturias (northwest of Spain), O. vulgaris artisanal fisheries are relatively well monitored and conditionally eco-labeled by the Marine Stewardship Council (MSC). Despite this, the Asturian octopus stocks have not been genetically assessed so far. In order to improve the current fishery plan and contrast the octopus eco-label validity in Asturias, 539 individuals from five regions of the O. vulgaris geographic distribution, including temporal samplings in Asturias, were collected and genotyped at thirteen microsatellite loci. All the samples under analysis were in agreement with Hardy-Weinberg expectations. Spatial levels of genetic differentiation were estimated using F-statistics, multidimensional scaling, and Bayesian analyses. Results suggested that the O. vulgaris consists of at least four genetically different stocks coming from two ancestral lineages. In addition, temporal analyses showed stability in terms of genetic variation and high NE (> 50) for several generations in different localities within Asturias, pointing out to indeed sustainable fishery exploitation levels. Even though, the current Asturias fishery plan shows no significant genetic damages to the stocks, the regional-specific management plans need systematic genetic monitoring schemes as part of an efficient and preventive regional fishery regulation strategy.


Assuntos
Octopodiformes , Humanos , Animais , Espanha , Octopodiformes/genética , Pesqueiros , Teorema de Bayes , Genótipo
2.
Oncogene ; 35(3): 314-22, 2016 Jan 21.
Artigo em Inglês | MEDLINE | ID: mdl-25867067

RESUMO

Tumor vessels are characterized by abnormal morphology and hyperpermeability that together cause inefficient delivery of chemotherapeutic agents. Although vascular endothelial growth factor has been established as a critical regulator of tumor angiogenesis, the role of mechanical signaling in the regulation of tumor vasculature or tumor endothelial cell (TEC) function is not known. Here we show that the mechanosensitive ion channel transient receptor potential vanilloid 4 (TRPV4) regulates tumor angiogenesis and tumor vessel maturation via modulation of TEC mechanosensitivity. We found that TECs exhibit reduced TRPV4 expression and function, which is correlated with aberrant mechanosensitivity towards extracellular matrix stiffness, increased migration and abnormal angiogenesis by TEC. Further, syngeneic tumor experiments revealed that the absence of TRPV4 induced increased vascular density, vessel diameter and reduced pericyte coverage resulting in enhanced tumor growth in TRPV4 knockout mice. Importantly, overexpression or pharmacological activation of TRPV4 restored aberrant TEC mechanosensitivity, migration and normalized abnormal angiogenesis in vitro by modulating Rho activity. Finally, a small molecule activator of TRPV4, GSK1016790A, in combination with anticancer drug cisplatin, significantly reduced tumor growth in wild-type mice by inducing vessel maturation. Our findings demonstrate TRPV4 channels to be critical regulators of tumor angiogenesis and represent a novel target for anti-angiogenic and vascular normalization therapies.


Assuntos
Carcinoma Pulmonar de Lewis/genética , Endotélio Vascular/patologia , Neovascularização Patológica/genética , Canais de Cátion TRPV/genética , Animais , Sinalização do Cálcio/genética , Carcinoma Pulmonar de Lewis/tratamento farmacológico , Carcinoma Pulmonar de Lewis/patologia , Linhagem Celular Tumoral , Proliferação de Células/efeitos dos fármacos , Cisplatino/administração & dosagem , Endotélio Vascular/efeitos dos fármacos , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Humanos , Leucina/administração & dosagem , Leucina/análogos & derivados , Camundongos , Neovascularização Patológica/tratamento farmacológico , Neovascularização Patológica/patologia , Sulfonamidas/administração & dosagem , Canais de Cátion TRPV/agonistas , Canais de Cátion TRPV/biossíntese , Fator A de Crescimento do Endotélio Vascular/genética
3.
J Nutr Biochem ; 26(10): 1041-9, 2015 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-26054778

RESUMO

Pancreatic islets, particularly insulin-secreting ß cells, share common characteristics with neurons. Glutamate is one of the major excitatory neurotransmitter in the brain and pancreas, and its action is mediated through glutamate receptors. In the present work, we analysed the role of vitamin D3 in the modulation of AMPA receptor subunit and their functional role in insulin release. Radio receptor binding study in diabetic rats showed a significant increase in AMPA receptor density. Insulin AMPA colabelling study showed an altered AMPA GluR2 and GluR4 subunit expression in the pancreatic beta cells. We also found lowered IP3 content and decreased IP3 receptor in pancreas of diabetic rats. The alterations in AMPA and IP3 receptor resulted in reduced cytosolic calcium level concentration, which further blocks Ca(2+)-mediated insulin release. Vitamin D3 supplementation restored the alteration in vitamin D receptor expression, AMPA receptor density and AMPA and IP3 receptor expression in the pancreatic islets that helps to restore the calcium-mediated insulin secretion. Our study reveals the antidiabetic property of vitamin D3 that is suggested to have therapeutic role through regulating glutamatergic function in diabetic rats.


Assuntos
Colecalciferol/administração & dosagem , Diabetes Mellitus Experimental/metabolismo , Receptores de Inositol 1,4,5-Trifosfato/análise , Insulina/sangue , Ilhotas Pancreáticas/química , Receptores de AMPA/análise , Animais , Glicemia/análise , Cálcio/análise , Diabetes Mellitus Experimental/sangue , Suplementos Nutricionais , Receptores de Inositol 1,4,5-Trifosfato/metabolismo , Masculino , Ensaio Radioligante , Ratos , Ratos Wistar , Receptores de AMPA/metabolismo
4.
J Biomed Sci ; 18: 31, 2011 May 12.
Artigo em Inglês | MEDLINE | ID: mdl-21569387

RESUMO

BACKGROUND: Hypoxia during the first week of life can induce neuronal death in vulnerable brain regions usually associated with an impairment of cognitive function that can be detected later in life. The neurobiological changes mediated through neurotransmitters and other signaling molecules associated with neonatal hypoxia are an important aspect in establishing a proper neonatal care. METHODS: The present study evaluated total GABA, GABAB receptor alterations, gene expression changes in GABAB receptor and glutamate decarboxylase in the cerebellum and brain stem of hypoxic neonatal rats and the resuscitation groups with glucose, oxygen and epinephrine. Radiolabelled GABA and baclofen were used for receptor studies of GABA and GABAB receptors respectively and Real Time PCR analysis using specific probes for GABAB receptor and GAD mRNA was done for gene expression studies. RESULTS: The adaptive response of the body to hypoxic stress resulted in a reduction in total GABA and GABAB receptors along with decreased GABAB receptor and GAD gene expression in the cerebellum and brain stem. Hypoxic rats supplemented with glucose alone and with oxygen showed a reversal of the receptor alterations and changes in GAD. Resuscitation with oxygen alone and epinephrine was less effective in reversing the receptor alterations. CONCLUSIONS: Being a source of immediate energy, glucose can reduce the ATP-depletion-induced changes in GABA and oxygenation, which helps in encountering hypoxia. The present study suggests that reduction in the GABAB receptors functional regulation during hypoxia plays an important role in central nervous system damage. Resuscitation with glucose alone and glucose and oxygen to hypoxic neonatal rats helps in protecting the brain from severe hypoxic damage.


Assuntos
Epinefrina/administração & dosagem , Glucose/administração & dosagem , Glutamato Descarboxilase/metabolismo , Oxigênio/administração & dosagem , Receptores de GABA-B/metabolismo , Ressuscitação/métodos , Ácido gama-Aminobutírico/metabolismo , Animais , Animais Recém-Nascidos , Tronco Encefálico/metabolismo , Cerebelo/metabolismo , Regulação da Expressão Gênica , Glutamato Descarboxilase/genética , Humanos , Hipóxia/metabolismo , Ratos , Ratos Wistar , Receptores de GABA-B/genética
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