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1.
J Neuroendocrinol ; 17(5): 314-20, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15869567

RESUMO

In zebrafish, the pineal gland is a photoreceptive organ that contains an intrinsic circadian oscillator and exhibits rhythmic arylalkylamine-N-acetyltransferase (zfaanat2) mRNA expression. In the present study, we investigated the role of light and of a clock gene, zperiod2 (zper2), in the development of this rhythm. Analysis of zfaanat2 mRNA expression in the pineal gland of 3-day-old zebrafish embryos after exposure to different photoperiodic regimes indicated that light is required for proper development of the circadian clock-controlled rhythmic expression of zfaanat2, and that a 1-h light pulse is sufficient to initiate this rhythm. Analysis of zper2 mRNA expression in zebrafish embryos exposed to different photoperiodic regimes indicated that zper2 expression is transiently up-regulated by light but is not regulated by the circadian oscillator. To establish the association between light-induced zper2 expression and light-induced clock-controlled zfaanat2 rhythm, zPer2 knock-down experiments were performed. The zfaanat2 mRNA rhythm, induced by a 1-h light pulse, was abolished in zPer2 knock-down embryos. These experiments indicated that light-induced zper2 expression is crucial for establishment of the clock-controlled zfaanat2 rhythm in the zebrafish pineal gland.


Assuntos
Arilalquilamina N-Acetiltransferase/metabolismo , Ritmo Circadiano/fisiologia , Proteínas do Olho/metabolismo , Proteínas de Peixes/metabolismo , Regulação da Expressão Gênica no Desenvolvimento/efeitos da radiação , Glândula Pineal/enzimologia , Peixe-Zebra/metabolismo , Animais , Arilalquilamina N-Acetiltransferase/genética , Arilalquilamina N-Acetiltransferase/efeitos da radiação , Biomarcadores/metabolismo , Ritmo Circadiano/genética , Ritmo Circadiano/efeitos da radiação , Proteínas do Olho/genética , Proteínas do Olho/efeitos da radiação , Feminino , Proteínas de Peixes/genética , Proteínas de Peixes/efeitos da radiação , Luz , Masculino , Proteínas Circadianas Period , Glândula Pineal/embriologia , Glândula Pineal/efeitos da radiação , RNA Mensageiro/análise , Peixe-Zebra/embriologia , Proteínas de Peixe-Zebra
2.
J Appl Physiol (1985) ; 90(6): 2411-9, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11356808

RESUMO

Low-energy laser irradiation (LELI) has been found to modulate biological processes. The present study investigated the effect of LELI on infarct size after chronic myocardial infarction (MI) and ischemia-reperfusion injury in rats. The left anterior descending (LAD) coronary artery was ligated in 83 rats to create MI or ischemia-reperfusion injury. The hearts of the laser-irradiated (LI) rats received irradiation after LAD coronary artery occlusion and 3 days post-MI. At 14, 21, and 45 days post-LAD coronary artery permanent occlusion, infarct sizes (percentage of left ventricular volume) in the non-laser-irradiated (NLI) rats were 52 +/- 12 (SD), 47 +/- 11, and 34 +/- 7%, respectively, whereas in the LI rats they were significantly lower, being 20 +/- 8, 15 +/- 6, and 10 +/- 4%, respectively. Left ventricular dilatation (LVD) in the chronic infarcted rats was significantly reduced (50-60%) in LI compared with NLI rats. LVD in the ischemia-reperfusion-injured LI rats was significantly reduced to a value that did not differ from intact normal noninfarcted rats. Laser irradiation caused a significant 2.2-fold elevation in the content of inducible heat shock proteins (specifically HSP70i) and 3.1-fold elevation in newly formed blood vessels in the heart compared with NLI rats. It is concluded that LELI caused a profound reduction in infarct size and LVD in the rat heart after chronic MI and caused complete reduction of LVD in ischemic-reperfused heart. This phenomenon may be partially explained by the cardioprotective effect of the HSP70i and enhanced angiogenesis in the myocardium after laser irradiation.


Assuntos
Terapia a Laser , Infarto do Miocárdio/radioterapia , Traumatismo por Reperfusão Miocárdica/radioterapia , Animais , Western Blotting , Vasos Coronários/fisiologia , Desmina/biossíntese , Proteínas de Choque Térmico/biossíntese , Imuno-Histoquímica , Ligadura , Masculino , Infarto do Miocárdio/metabolismo , Infarto do Miocárdio/patologia , Traumatismo por Reperfusão Miocárdica/metabolismo , Traumatismo por Reperfusão Miocárdica/patologia , Neovascularização Fisiológica/efeitos da radiação , Ratos , Ratos Sprague-Dawley
3.
Comp Biochem Physiol B Biochem Mol Biol ; 112(1): 147-51, 1995 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-7584842

RESUMO

Cathepsin D was purified 750-fold from a homogenate of Cyprinus carpio muscles. The purified enzyme has a molecular weight of 36,000, is inhibited by pepstatin and is active between pH 2.7 and 3.7 when tested on hemoglobin as the substrate. It consists of two isoenzymes with pIs of 5.65 and 6.1, respectively. The mode of cleavage of the beta chain of oxidized insulin was determined by analysis of the N-terminal amino acids of the cleaved peptides. The major points of cleavage of the beta chain of oxidized insulin are 56% at Tyr16-Leu17 and 40% at Phe25-Tyr26. The minor points of cleavage are at Leu15-Tyr16, Phe24-Phe25, Gly23-Phe24, Leu11-Val12, Ala14-Leu15 and Gln4-His5.


Assuntos
Carpas/metabolismo , Catepsina D/isolamento & purificação , Músculos/enzimologia , Sequência de Aminoácidos , Animais , Catepsina D/análise , Catepsina D/metabolismo , Hidrólise , Insulina/metabolismo , Dados de Sequência Molecular , Peso Molecular , Pepstatinas/metabolismo , Inibidores de Proteases/metabolismo , Especificidade por Substrato
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