RESUMO
We examined the effect of occlusal disharmony in senescence-accelerated (SAMP8) mice on plasma corticosterone levels, spatial learning in the water maze, fos induction, hippocampal neuron number, expression of glucocorticoid receptors (GR) and glucocorticoid receptor messenger ribonucleic acid (GRmRNA) in hippocampus and inhibitor of glucocorticoid (metyrapone). Bite-raised aged mice had significantly greater plasma corticosterone levels than age-matched control mice as well as impaired spatial memory and decreased Fos induction and a number of neurons in hippocampus. GR and GRmRNA expressions were significantly decreased in aged bite-raised mice compared with age-matched control mice. Pretreatment with metyrapone inhibited not only the bite-raised induced increase in plasma corticosterone levels, but also the reduction in the number of hippocampal neurons and impaired spatial learning. These datas suggest that the bite-raised condition may enhance the aging process in hippocampus, thereby leading to impairment of spatial memory by stress.
Assuntos
Glucocorticoides/sangue , Hipocampo/fisiopatologia , Má Oclusão/complicações , Memória/fisiologia , Estresse Fisiológico/etiologia , Envelhecimento/fisiologia , Animais , Glucocorticoides/antagonistas & inibidores , Hipocampo/citologia , Má Oclusão/metabolismo , Má Oclusão/fisiopatologia , Camundongos , Proteínas Proto-Oncogênicas c-fos/metabolismo , Receptores de Glucocorticoides/metabolismo , Comportamento Espacial/fisiologia , Estresse Fisiológico/metabolismo , Estresse Fisiológico/fisiopatologiaRESUMO
The tumour suppressor p53 is activated following stress and initiates a heterogeneous response in a cell-, tissue- and stress-dependent manner. This heterogeneity is reflected in the different physiological outcomes that follow p53 activation. One mechanism that may contribute to this variability is the promoter selectivity of p53 target genes. p53 is at the hub of numerous signalling pathways that are triggered in response to particular stresses, all of which can leave their mark on p53 by way of post-translational modifications and interactions with cofactors. The precise combination of these marks, much like the bars in a barcode, dictates the behaviour of p53 in any given situation.
Assuntos
Estresse Fisiológico/metabolismo , Proteína Supressora de Tumor p53/metabolismo , Animais , Humanos , Especificidade de Órgãos , Transporte Proteico , Proteína Supressora de Tumor p53/genéticaRESUMO
The disruption of endoplasmic reticulum function leads to an accumulation of unfolded proteins, which results in endoplasmic reticulum stress. In the present study, we investigated the effect of vanadate on such stress. Endoplasmic reticulum stress increased glucose-regulated protein 78 (GRP78) and CCAAT/enhancer-binding protein homologous protein (CHOP) expressions in glial cell cultures. We found that vanadate inhibited the endoplasmic reticulum stress-induced increase in GRP78 and CHOP expressions at both mRNA and protein levels. Thus, these results suggest that vanadate modulates endoplasmic reticulum stress responses and that novel vanadate-responsive protein(s) might be involved in these processes.
Assuntos
Retículo Endoplasmático/efeitos dos fármacos , Estresse Fisiológico/metabolismo , Vanadatos/farmacologia , Animais , Western Blotting , Linhagem Celular Tumoral , Chaperona BiP do Retículo Endoplasmático , Gliceraldeído-3-Fosfato Desidrogenases/metabolismo , Proteínas de Choque Térmico/biossíntese , Camundongos , Camundongos Endogâmicos C57BL , Chaperonas Moleculares/biossíntese , Neuroglia/efeitos dos fármacos , Neuroglia/metabolismo , RNA Mensageiro/biossíntese , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Fator de Transcrição CHOP/biossíntese , Tirosina/metabolismoRESUMO
MICA and MICB are stress-induced ligands recognized by the activating receptor NKG2D. A microRNA encoded by human cytomegalovirus downregulates MICB expression by targeting a specific site in the MICB 3' untranslated region. As this site is conserved among different MICB alleles and a similar site exists in the MICA 3' untranslated region, we speculated that these sites are targeted by cellular microRNAs. Here we identified microRNAs that bound to these MICA and MICB 3' untranslated region sequences and obtained data suggesting that these microRNAs maintain expression of MICA and MICB protein under a certain threshold and facilitate acute upregulation of MICA and MICB during cellular stress. These microRNAs were overexpressed in various tumors and we demonstrate here that they aided tumor avoidance of immune recognition.
Assuntos
Antígenos de Histocompatibilidade Classe I/metabolismo , MicroRNAs/fisiologia , Receptores Imunológicos/metabolismo , Estresse Fisiológico/imunologia , Antígenos de Superfície/metabolismo , Linhagem Celular , Vetores Genéticos , Antígenos de Histocompatibilidade Classe I/química , Humanos , MicroRNAs/imunologia , Subfamília K de Receptores Semelhantes a Lectina de Células NK , Receptores de Células Matadoras Naturais , Estresse Fisiológico/genética , Estresse Fisiológico/metabolismoRESUMO
The immune, endocrine and nervous systems are closely interrelated, which allows the organism to respond to different types of stress such as infection. Chronic infectious and inflammatory conditions are often accompanied by an impaired reproductive function. Leptin, a hormone produced by adipose tissue, exerts a regulatory function on the reproductive axis. It has homology with other proinflammatory cytokines and could be modified by lipopolysaccharide (LPS). Therefore, these studies were designed to investigate the effect of LPS administration on the neuroendocrine mechanisms involved in the regulation of the reproductive axis during sexual maturation. Fifteen- and 30-day-old female rats were injected with a single dose of LPS 250 microg/kg (i.p.) and then nitric oxide synthase (NOS) activity, hypothalamic excitatory/inhibitory amino acids and Gn-RH content, serum LH and leptin concentration were studied. In 15-day-old female rats LPS treatment did not modify hypothalamic inducible (iNOS) and constitutive (cNOS) NOS activity, Gn-RH, glutamate (GLU) and GABA content. Also serum LH and leptin levels were not modified. In 30-day-old rats LPS increased iNOS and cNOS activity (p < 0.001) and hypothalamic Gn-RH content (p < 0.001). At this age hypothalamic GABA content was significantly decreased (p < 0.001) without changes in GLU content, and serum LH (p < 0.001) and leptin (p < 0.0001) decreased significantly. In summary, current studies have demonstrated that LPS administration to 15- and 30-day-old female rats results in a different response of the hypothalamus-pituitary-gonadal axis and of the adipose tissue, demonstrating an ontogenic response of the immune-neuroendocrine system to LPS administration.
Assuntos
Infecções Bacterianas/imunologia , Leptina/imunologia , Neuroimunomodulação/imunologia , Sistemas Neurossecretores/imunologia , Reprodução/imunologia , Maturidade Sexual/imunologia , Tecido Adiposo/imunologia , Tecido Adiposo/metabolismo , Envelhecimento/imunologia , Envelhecimento/metabolismo , Animais , Feminino , Ácido Glutâmico/imunologia , Ácido Glutâmico/metabolismo , Hormônio Liberador de Gonadotropina/imunologia , Hormônio Liberador de Gonadotropina/metabolismo , Sistema Hipotálamo-Hipofisário/imunologia , Sistema Hipotálamo-Hipofisário/metabolismo , Hipotálamo/imunologia , Hipotálamo/metabolismo , Mediadores da Inflamação/farmacologia , Leptina/sangue , Lipopolissacarídeos/farmacologia , Hormônio Luteinizante/sangue , Hormônio Luteinizante/imunologia , Sistemas Neurossecretores/metabolismo , Sistemas Neurossecretores/fisiopatologia , Óxido Nítrico Sintase/imunologia , Óxido Nítrico Sintase/metabolismo , Ratos , Ratos Wistar , Estresse Fisiológico/imunologia , Estresse Fisiológico/metabolismo , Estresse Fisiológico/fisiopatologia , Regulação para Cima/imunologia , Ácido gama-Aminobutírico/imunologia , Ácido gama-Aminobutírico/metabolismoRESUMO
The interaction between microenvironmental components and tumor cells is bidirectional. Tumor cells and their products are capable of regulating and altering gene expression in nontumor cells residing in or infiltrating into the microenvironment and exert selective pressures on such cells, thereby shaping their phenotype. Conversely, microenvironmental components regulate gene expression in tumor cells thereby directing the tumor into one or several possible molecular evolution pathways, some of which may lead to metastasis. This review summarizes six instances in which the tumor liaises with different components of its microenvironment. These liaisons result, in most cases, in enhanced tumor progression. In these cases (responses of tumor and nontumor cells to microenvironmental stress, the interaction of the tumor with fibroblasts, endothelial cells and macrophages, the formation of the metastatic niche, and the interaction of the tumor with immunoglobulins) the tumor, directly or indirectly, alters the phenotype of its interaction partners thereby enlisting them to promote its progression. Does the tumor need all these pathways to form metastasis? Is there a hierarchy of interactions with respect to impact on tumor progression? These questions remain open. They may be answered by approaches employed in the analysis of hypercomplex systems.
Assuntos
Comunicação Celular/fisiologia , Neoplasias/patologia , Animais , Antígenos de Neoplasias/imunologia , Endotélio/patologia , Endotélio/fisiologia , Fibroblastos/patologia , Fibroblastos/fisiologia , Humanos , Imunoglobulinas/fisiologia , Macrófagos/patologia , Macrófagos/fisiologia , Metástase Neoplásica , Neovascularização Patológica/patologia , Estresse Fisiológico/metabolismo , Estresse Fisiológico/patologiaRESUMO
BACKGROUND: The placenta is an important site for iron metabolism in humans. It transfers iron from the mother to the fetus. One of the major iron transport proteins is transferrin, which is a blood plasma protein crucial for iron uptake. Its localization and expression may be one of the markers to distinguish placental dysfunction. METHODS: In the experimental study we used antibody preparation, mass spectrometric analysis, biochemical and immunocytochemical methods for characterization of transferrin expression on the human choriocarcinoma cell line JAR (JAR cells), placental lysates, and cryostat sections. Newly designed monoclonal antibody TRO-tf-01 to human transferrin was applied on human placentae from normal (n = 3) and abnormal (n = 9) pregnancies. RESULTS: Variations of transferrin expression were detected in villous syncytiotrophoblast, which is in direct contact with maternal blood. In placentae from normal pregnancies, the expression of transferrin in the syncytium was significantly lower (p < 0.001) when compared to placentae from abnormal ones (gestational diabetes, pregnancy induced hypertension, drug abuse). CONCLUSION: These observations suggest that in the case of abnormal pregnancies, the fetus may require higher levels of transferrin in order to prevent iron depletion due to the stress from the placental dysfunction.
Assuntos
Doenças Placentárias/metabolismo , Placenta/metabolismo , Complicações na Gravidez/metabolismo , Transferrina/metabolismo , Adulto , Anticorpos Monoclonais , Epitopos , Feminino , Humanos , Imuno-Histoquímica , Ferro/metabolismo , Masculino , Modelos Biológicos , Projetos Piloto , Gravidez , Estresse Fisiológico/metabolismo , Transferrina/imunologiaRESUMO
Corticotropin-releasing hormone (CRH) plays a central role in controlling stress response. In this study, we aimed to identify the regulatory effect of estrogen receptor (ER) on CRH and the underlying mechanism. We investigated the regulation of CRH mRNA in the BE(2)-C cell line, a human neuroblastoma cell line which express endogenous CRH. Quantitative reverse transcriptase-polymerase chain reactions showed that in the presence of estradiol overexpressing ER alpha or ER beta in BE(2)-C cells increased the transcription of CRH. Chromatin immunoprecipitation assays in this cell line also showed that both ER alpha and ER beta can be recruited to the CRH promoter with the treatment of estradiol. However, electrophoretic mobility shift assays did not show direct binding between estrogen receptors and two estrogen response elements (ERE) half sites in the CRH promoter. To clarify the regulatory mechanism, site-directed mutagenesis and reporter gene assay in the CHO cell line were used. When the ERE half sites and the cAMP regulatory element (CRE) in the CRH promoter were disrupted, ER-mediated up-regulation of CRH promoter activity reduced. Between the two ERE half sites studied, the -316 ERE half site contributed more to the constitutive CRH expression induced by ER. In summary, our results confirm the stimulation of ER alpha and ER beta on CRH expression and demonstrate the important roles of the ERE half sites and CRE for the action of ER alpha and ER beta.
Assuntos
Encéfalo/metabolismo , Hormônio Liberador da Corticotropina/genética , Receptor alfa de Estrogênio/metabolismo , Receptor beta de Estrogênio/metabolismo , Sistema Hipotálamo-Hipofisário/metabolismo , Transdução de Sinais/genética , Fator 2 Ativador da Transcrição/genética , Fator 2 Ativador da Transcrição/metabolismo , Corticosteroides/metabolismo , Animais , Células CHO , Linhagem Celular Tumoral , Hormônio Liberador da Corticotropina/biossíntese , Cricetinae , Cricetulus , Estradiol/metabolismo , Estradiol/farmacologia , Receptor alfa de Estrogênio/genética , Receptor beta de Estrogênio/genética , Humanos , Camundongos , Regiões Promotoras Genéticas/efeitos dos fármacos , Regiões Promotoras Genéticas/genética , RNA Mensageiro/efeitos dos fármacos , RNA Mensageiro/metabolismo , Ratos , Elementos de Resposta/efeitos dos fármacos , Elementos de Resposta/genética , Estresse Fisiológico/genética , Estresse Fisiológico/metabolismo , Estresse Fisiológico/fisiopatologia , Ativação Transcricional/efeitos dos fármacos , Ativação Transcricional/genéticaRESUMO
Two experiments were conducted to investigate the effect of acute preslaughter stress mimicked by exogenous corticosterone (CORT) administration on postmortem muscle metabolism of broiler chickens. Altered protein metabolism, glycogen depletion, and meat quality characteristics were investigated in the musculus pectoralis major (PM) and musculus biceps femoris of broiler chickens. Results showed that CORT administration resulted in increased proteolysis and gluconeogenesis, whereas the capacity for protein synthesis was not obviously changed. Plasma levels of glucose, urate, and total free amino acids were all significantly decreased by CORT treatment. The effect of CORT administration on muscle R-values remained uncertain. The initial muscle buffer capacity was increased by CORT treatment in both musculus pectoralis major and musculus biceps femoris. The results suggested that the acute premortem up-regulation of CORT decreased muscle ultimate pH by increasing the antemortem muscle glycogen content and its depletion rate postmortem, which in turn induced a decrease in water-holding capacity. Muscle buffering capacity might be altered by CORT administration, and its involvement in the change of muscle pH needs to be investigated further.
Assuntos
Galinhas , Corticosterona/farmacologia , Carne/análise , Músculo Esquelético/efeitos dos fármacos , Músculo Esquelético/metabolismo , Estresse Fisiológico/metabolismo , Estresse Fisiológico/veterinária , Animais , Biópsia/veterinária , Glicemia/metabolismo , Ácidos Graxos não Esterificados/sangue , Feminino , Glicogênio/metabolismo , Concentração de Íons de Hidrogênio , Ácido Láctico/sangue , Masculino , Distribuição Aleatória , Triglicerídeos/sangue , Ácido Úrico/sangueRESUMO
Stress is a major risk factor in drug addiction development and relapse. Virtually all drugs of abuse act by increasing extracellular dopamine levels in the striatum. To gain an understanding of the interaction between stress and drug exposure, we studied the effects of concomitant chronic nicotine and chronic stress exposure on mouse striatal dopamine levels. C57Bl6/J mice were treated with nicotine in the drinking water or control solution for at least 6 weeks. Some mice were chronically stressed by daily exposure to cold, shaking or restrain. Nicotine-treated mice showed up-regulation of epibatidine binding in several brain regions. In mice treated with both chronic nicotine and stress, epibatidine binding was increased in all studied areas except the dorsal striatum. Therefore, microdialysis was used to measure extracellular dopamine levels in the dorsal striatum of mice chronically treated with nicotine, stress, or both. To have a measure of striatal response to different challenges, we performed microdialysis after acute injection of saline, nicotine, and cocaine. Chronic nicotine enhanced nicotine-dependent dopamine release, while chronic stress blunted the response to cocaine. When mice were subjected to both chronic nicotine and chronic stress, nicotine- and cocaine-dependent dopamine release was undistinguishable from that of control animals. In conclusion, our data suggest that chronic stress and chronic nicotine counteract each other's effect on dopamine release in the striatum. This effect might be mediated by changes in nicotinic acetylcholine receptor up-regulation. This "normalization" of striatal function when both nicotine and stress are present might help explain the comorbidity between stress-related disorders and drug abuse.
Assuntos
Corpo Estriado/efeitos dos fármacos , Corpo Estriado/fisiopatologia , Nicotina/farmacologia , Agonistas Nicotínicos/farmacologia , Estresse Fisiológico/patologia , Análise de Variância , Animais , Compostos Bicíclicos Heterocíclicos com Pontes/metabolismo , Dopamina/metabolismo , Feminino , Técnicas In Vitro , Isótopos de Iodo/metabolismo , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Ligação Proteica/efeitos dos fármacos , Piridinas/metabolismo , Estresse Fisiológico/metabolismoRESUMO
Hypoxia-inducible transcription factor-1 (HIF-1) is the most important component of cellular and molecular adaptive responses to hypoxia. We aimed to analyze effects of systemic hypoxia and CO exposure on the oxygen-regulated alpha-subunit of HIF-1 and HIF-1-dependent vasoactive target genes in rat brain. Brains of adult Sprague-Dawley rats were investigated after incubation for 3 and 12 h under normoxia, hypoxia (8% O(2)) and CO 0.1% (n = 10 per group). Upon 3 h of exposure, hypoxia and CO-induced accumulation of HIF-1alpha protein in brain homogenates assessed by Western blot analysis. In contrast to hypoxia HIF-1alpha signals decreased markedly during 12 h-exposure to CO. By immunohistochemistry, intensive HIF-1alpha-positive staining was found in neurons of the cortex and hippocampus. Cerebral expression of vasoactive target genes adrenomedullin (ADM) and vascular endothelial growth factor (VEGF) showed up-regulation during both hypoxia and CO exposure indicating functional activation of HIF-1. Hypoxia increased ADM (P < 0.05) and VEGF mRNA levels within 3 h (P < 0.01) which persisted up to 12 h of exposure (ADM, P < 0.05; VEGF, P < 0.001). Similarly, CO inhalation led to early up-regulation of VEGF (3 h: P < 0.05; 12 h: P < 0.01), but a more delayed increase of ADM mRNA levels (3 h: n.s., 12 h: P < 0.01). We suggest that CO-induced oxygen deprivation is a potent stimulus to cerebral HIF-1-regulated hypoxic stress responses even though its effects are more transient than exposure to hypoxia.
Assuntos
Adrenomedulina/metabolismo , Encéfalo/metabolismo , Hipóxia Encefálica/metabolismo , Subunidade alfa do Fator 1 Induzível por Hipóxia/metabolismo , Estresse Fisiológico/metabolismo , Fator A de Crescimento do Endotélio Vascular/metabolismo , Adrenomedulina/genética , Animais , Western Blotting , Monóxido de Carbono , Circulação Cerebrovascular , Modelos Animais de Doenças , Hipóxia Encefálica/induzido quimicamente , Hipóxia Encefálica/genética , Hipóxia Encefálica/fisiopatologia , Subunidade alfa do Fator 1 Induzível por Hipóxia/genética , Imuno-Histoquímica , Masculino , RNA Mensageiro/metabolismo , Ratos , Ratos Sprague-Dawley , Estresse Fisiológico/genética , Estresse Fisiológico/fisiopatologia , Fatores de Tempo , Regulação para Cima , Fator A de Crescimento do Endotélio Vascular/genéticaRESUMO
Membrane type 1-matrix metalloproteinase (MT1-MMP) plays a key role in extracellular matrix remodeling, endothelial cell (EC) migration, and angiogenesis. Whereas cyclic strain (CS) increases MT1-MMP expression, shear stress (SS) decreases MT1-MMP expression. The aim of this study was to determine if changes in levels of Sp1 phosphorylation induced by protein kinase Czeta (PKCzeta) in ECs exposed to SS but not CS are important for MT1-MMP expression. The results showed that SS increased Sp1 phosphorylation, which could be inhibited by pretreatment with PKCzeta inhibitors. In the presence of PKCzeta inhibitors, the SS-mediated decrease in MT1-MMP protein expression was also abolished. These data demonstrate that increased affinity of Sp1 for MT1-MMP's promoter site occurs as a consequence of PKCzeta-induced phosphorylation of Sp1 in response to SS, increasing Sp1 binding affinity for the promoter site, preventing Egr-1 binding, and consequently decreasing MT1-MMP expression.
Assuntos
Células Endoteliais/enzimologia , Metaloproteinase 14 da Matriz/metabolismo , Proteína Quinase C/metabolismo , Fator de Transcrição Sp1/metabolismo , Estresse Fisiológico/metabolismo , Animais , Técnicas de Cultura de Células , Células Cultivadas , Meios de Cultura Livres de Soro , Endotélio Vascular/citologia , Isoenzimas/genética , Isoenzimas/metabolismo , Masculino , Modelos Biológicos , Fosforilação , Proteína Quinase C/análise , Proteína Quinase C/genética , Ratos , Ratos Sprague-Dawley , Fator de Transcrição Sp1/genética , Estresse MecânicoRESUMO
BACKGROUND: We designed and tested, in vitro, an adenoviral construct containing the feline interleukin-12 (IL-12) gene under control of the heat-inducible promoter HSP70B. This construct, AdhspfIL12, was used in a phase I trial in feline soft tissue sarcomas. During the course of our experiments, we noted that IL-12 was being produced in the transfected Crandell Feline Kidney (CrFK) cells under certain conditions even in the absence of hyperthermia. This observation was further explored to identify the cause of this unintended HSP70B induction. MATERIALS AND METHODS: We used real-time PCR as a sensitive method to quantitatively detect the presence of even small amounts of IL-12 mRNA. This served as a surrogate indicator of HSP70B induction. Various conditions were tested to induce the heat shock promoter, including nutritional deprivation, radiation and changes in pH. RESULTS: Nutritional stresses, specifically the absence of glucose and glutamine, could induce the heat shock promoter, thus, resulting in production of the downstream gene product. Other factors known to trigger the heat shock response, pH change, and reactive oxygen species production were also studied but were not found to contribute to heat shock promoter induction in our setting. CONCLUSIONS: The human heat shock promoter (HSP70B) is reported to be an efficient and tightly regulated promoter. We discovered, using sensitive real-time PCR techniques, that it can also be induced in response to cellular nutrient stresses. The pros and cons of this phenomenon and its implications for cancer gene therapy are discussed.
Assuntos
Terapia Genética/métodos , Proteínas de Choque Térmico HSP70/genética , Interleucina-12/biossíntese , Regiões Promotoras Genéticas , Estresse Fisiológico/metabolismo , Ativação Transcricional , Adenoviridae/genética , Animais , Antimitóticos/farmacologia , Afidicolina/farmacologia , Gatos , Linhagem Celular , Proliferação de Células , Meios de Cultura/metabolismo , Terapia Genética/efeitos adversos , Vetores Genéticos , Glucose/deficiência , Glutamina/deficiência , Humanos , Concentração de Íons de Hidrogênio , Hipertermia Induzida , Interleucina-12/genética , Reação em Cadeia da Polimerase , RNA Mensageiro/biossíntese , Espécies Reativas de Oxigênio/metabolismo , Estresse Fisiológico/genética , Fatores de Tempo , Ativação Transcricional/efeitos dos fármacos , TransfecçãoRESUMO
OBJECTIVE: The endothelin (ET) system is influenced by a variety of stress conditions in many tissues. However, the effects of nutrient stress conditions on ET expression and its function are not well understood in the intestinal tract, while ET-1 gene expression and peptide were found in the intestinal tract. The aim of this study was to investigate the effect of feeding and fasting on the expression of ET-1 and short-circuit current (Isc) induced by ET-1 in mouse colon. MATERIAL AND METHODS: Mice were fed freely, fasted for 48 h, and re-fed after fasting, respectively. ET-1 mRNA levels and peptide concentrations were analyzed using real-time polymerase chain reaction (PCR) and sandwich ELISA, respectively. Isc of epithelial tissue was measured under short-circuit conditions using a Ussing chamber. RESULTS: ET-1 mRNA expression and peptide concentrations in epithelial colonic tissue were significantly increased 48 h after fasting, and decreased within 2 h of re-feeding after a 48-h fast. Furthermore, the addition of ET-1 to the serosal but not the mucosal side increased Isc in colonic epithelia. An increase in Isc was caused by chloride ion (Cl(-)) secretion because Isc induced by ET-1 was blocked by bumetanide and Cl(- -) free conditions. In addition, an increase in Isc induced by ET-1 in colon excised from fasted mice was much lower than that obtained from free-fed mice. CONCLUSIONS: Gene expression, peptide concentration, and the function of ET-1 in mouse colonic epithelia are regulated by nutrient stress.
Assuntos
Colo/metabolismo , Endotelina-1/metabolismo , Jejum , Regulação da Expressão Gênica , Mucosa Intestinal/metabolismo , Estresse Fisiológico/metabolismo , Animais , Bumetanida/farmacologia , ATPases Transportadoras de Cálcio/antagonistas & inibidores , Cloretos/antagonistas & inibidores , Cloretos/metabolismo , Colo/fisiologia , Eletrofisiologia , Endotelina-1/genética , Endotelina-1/fisiologia , Inibidores Enzimáticos/farmacologia , Epitélio/metabolismo , Mucosa Intestinal/fisiologia , Masculino , Camundongos , Camundongos Endogâmicos ICR , Músculo Liso/metabolismo , Reação em Cadeia da Polimerase , RNA Mensageiro/metabolismo , Tapsigargina/farmacologiaRESUMO
STAT3 is a major signaling molecule for many neurotrophic factors but its direct role in the protection of neurons in response to stress has not been addressed. We have studied the role of STAT3 in protecting retinal neurons from damage induced by ischemia/reperfusion and glutamate excitotoxicity by using adenovirus constructs to introduce active, normal or inactive STAT3 into retinal ganglion cells in culture and cells of the ganglion cell layer in the intact retina. Transient ischemia/reperfusion was induced in adult CD1 mice by elevating the intraocular pressure to the equivalent of 120mmHg for 60min, followed by a return to normal pressure. The levels, activation and distribution of STAT3 protein were evaluated by Western blot and immunocytochemistry. A transient peak of STAT3 activation was seen at 24h post ischemia and a strong increase in STAT3 protein levels 24h later. The increase in levels of STAT3 was detected in both ganglion cell bodies and processes in the plexiform layers by immunocytochemistry. The time course of STAT3 increase was slower than the time course of ganglion cell death as measured by TUNEL assay. Intravitreal injection of NMDA led to peak increases in activated STAT3 and STAT3 at 12 and 24h post insult respectively. Purified RGCs were infected with recombinant wild-type STAT3, constitutively active and dominant negative forms of STAT3 adenoviruses or control empty virus and then treated with glutamate. Surviving infected cells were counted 24 and 48h later. Infection with constitutively active STAT3 gave substantial protection when compared to the other constructs. Similarly, intravitreal injection of constitutively active STAT3 adenovirus one day before ischemia-reperfusion resulted in a decreased neural cell death in the ganglion cell layer compared with GFP adenovirus control. Our results suggest that persistent activation of STAT3 by neurotrophic factors provides strong neuroprotection and will be an effective strategy in a number of chronic retinal diseases.
Assuntos
Doenças Retinianas/patologia , Células Ganglionares da Retina/metabolismo , Fator de Transcrição STAT3/fisiologia , Estresse Fisiológico/patologia , Adenoviridae/genética , Animais , Sobrevivência Celular , Células Cultivadas , Citoproteção/fisiologia , Modelos Animais de Doenças , Agonistas de Aminoácidos Excitatórios , Ácido Glutâmico/farmacologia , Camundongos , Camundongos Endogâmicos , N-Metilaspartato , Ratos , Ratos Long-Evans , Traumatismo por Reperfusão/metabolismo , Traumatismo por Reperfusão/patologia , Doenças Retinianas/metabolismo , Células Ganglionares da Retina/efeitos dos fármacos , Células Ganglionares da Retina/patologia , Vasos Retinianos/metabolismo , Vasos Retinianos/patologia , Fator de Transcrição STAT3/metabolismo , Estresse Fisiológico/metabolismoRESUMO
The survival of all organisms depends upon their ability to overcome stressful conditions, an ability that involves adaptive changes in cells and molecules. Findings from studies of animal models and human populations suggest that hormesis (beneficial effects of low levels of stress) is an effective means of protecting against many different diseases including diabetes, cardiovascular disease, cancers and neurodegenerative disorders. Such stress resistance mechanisms can be bolstered by diverse environmental factors including exercise, dietary restriction, cognitive stimulation and exposure to low levels of toxins. Some commonly used vitamins and dietary supplements may also induce beneficial stress responses. Several interrelated cellular signaling molecules are involved in the process of hormesis. Examples include the gases oxygen, carbon monoxide and nitric oxide, the neurotransmitter glutamate, the calcium ion and tumor necrosis factor. In each case low levels of these signaling molecules are beneficial and protect against disease, whereas high levels can cause the dysfunction and/or death of cells. The cellular and molecular mechanisms of hormesis are being revealed and include activation of growth factor signaling pathways, protein chaperones, cell survival genes and enzymes called sirtuins. Knowledge of hormesis mechanisms is leading to novel approaches for preventing and treating a range of human diseases.
Assuntos
Adaptação Fisiológica , Imunidade Inata/fisiologia , Estresse Fisiológico/metabolismo , Xenobióticos/farmacologia , Animais , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Homeostase/fisiologia , Humanos , Imunidade Inata/efeitos dos fármacos , Extratos Vegetais/metabolismo , Extratos Vegetais/farmacologia , Estresse Fisiológico/fisiopatologiaAssuntos
Bloqueio Nervoso , Estresse Fisiológico/prevenção & controle , Procedimentos Cirúrgicos Operatórios , Humanos , Procedimentos Cirúrgicos Minimamente Invasivos/efeitos adversos , Estresse Fisiológico/metabolismo , Estresse Fisiológico/fisiopatologia , Procedimentos Cirúrgicos Operatórios/efeitos adversosRESUMO
The interaction between the stress axis and endogenous opioid systems has gained substantial attention, because it is increasingly recognized that stress alters individual sensitivity to opiates. One site at which opiates and stress substrates may interact to have global effects on behavior is within the locus coeruleus (LC). We have previously described interactions of several opioid peptides [e.g., proopiomelanocortin, enkephalin (ENK)] with the stress-related peptide corticotropin-releasing factor (CRF) in the LC. To examine further the interactions among dynorphin (DYN), ENK, and CRF in the LC, sections were processed for detection of DYN and CRF or DYN and ENK in rat brain. DYN- and CRF-containing axon terminals overlapped noradrenergic dendrites in this region. Dual immunoelectron microscopy showed coexistence of DYN and CRF; 35% of axon terminals containing DYN were also immunoreactive for CRF. In contrast, few axon terminals contained both DYN and ENK. A potential DYN/CRF afferent is the central nucleus of the amygdala (CeA). Dual in situ hybridization showed that, in CeA neurons, 31% of DYN mRNA-positive cells colocalized with CRF mRNA, whereas 53% of CRF mRNA-containing cells colocalized with DYN mRNA. Finally, to determine whether limbic DYN afferents target the LC, the CeA was electrolytically lesioned. Light-level densitometry of DYN labeling in the LC showed a significant decrease in immunoreactivity on the side of the lesion. Taken together, these data indicate that DYN- and CRF-labeled axon terminals, most likely arising from amygdalar sources, are positioned dually to affect LC function, whereas DYN and ENK function in parallel.
Assuntos
Tonsila do Cerebelo/química , Tonsila do Cerebelo/fisiologia , Dinorfinas/análise , Locus Cerúleo/química , Peptídeos/química , Estresse Fisiológico , Animais , Dinorfinas/fisiologia , Vias Eferentes/química , Vias Eferentes/fisiologia , Locus Cerúleo/fisiologia , Masculino , Peptídeos/fisiologia , Ratos , Ratos Sprague-Dawley , Estresse Fisiológico/metabolismoRESUMO
The heat shock proteins (Hsps) have been implicated in a variety of neurodegenerative diseases in which the underlying pathology is protein aggregation. Here, we studied the heat shock response in familial amyloidotic polyneuropathy (FAP), a neurodegenerative disease caused by aggregation and extracellular tissue deposition of mutated transthyretin (TTR). We observed greater expression of Hsp27 and Hsp70 related to the presence of extracellular TTR aggregates in human FAP nerve, skin, and salivary gland biopsies than in normal controls. Transthyretin aggregates did not colocalize with Hsp, suggesting that extracellular TTR tissue deposits induce an intracellular stress response. Moreover, the heat shock transcription factor 1 was upregulated and localized to nuclei in affected tissues. Transgenic mice expressing the V30M mutant form of TTR similarly showed the presence of TTR deposits, induced activation of heat shock transcription factor 1, and increased synthesis of Hsp. Furthermore, the addition of toxic TTR aggregates to cultures of human and rodent neuroblastoma cell lines induced upregulation of Hsp70 and Hsp27. Taken together, these novel findings suggest new avenues for research on pathogenic mechanisms in FAP and identify the heat shock response as a potential pharmacologic treatment target for FAP.
Assuntos
Neuropatias Amiloides Familiares/metabolismo , Proteínas de Choque Térmico/metabolismo , Resposta ao Choque Térmico , Pré-Albumina/metabolismo , Neuropatias Amiloides Familiares/patologia , Neuropatias Amiloides Familiares/fisiopatologia , Animais , Biópsia , Linhagem Celular Tumoral , Proteínas de Ligação a DNA/metabolismo , Proteínas de Choque Térmico HSP27 , Proteínas de Choque Térmico HSP72/metabolismo , Fatores de Transcrição de Choque Térmico , Resposta ao Choque Térmico/fisiologia , Humanos , Corpos de Inclusão/genética , Corpos de Inclusão/metabolismo , Corpos de Inclusão/patologia , Camundongos , Camundongos Transgênicos , Chaperonas Moleculares , Proteínas de Neoplasias/metabolismo , Nervos Periféricos/metabolismo , Nervos Periféricos/patologia , Nervos Periféricos/fisiopatologia , Pré-Albumina/genética , Pré-Albumina/farmacologia , Glândulas Salivares/inervação , Glândulas Salivares/metabolismo , Glândulas Salivares/patologia , Pele/inervação , Pele/metabolismo , Pele/patologia , Estresse Fisiológico/genética , Estresse Fisiológico/metabolismo , Estresse Fisiológico/fisiopatologia , Fatores de Transcrição/metabolismo , Regulação para Cima/fisiologiaRESUMO
Patients with adrenal insufficiency (AI) require additional glucocorticoid doses during surgery or medical illness, but there is no universally accepted regimen for glucocorticoid supplementation therapy. The high doses and long duration of glucocorticoid coverage that have traditionally been used do not reflect the hypothalamic-pituitary-adrenal response to surgical stress and medical illness in normal people. While the optimal dose and duration of supplementation therapy have not been established, our recommendations are based on extrapolation from what constitutes a normal cortisol response to stress, on expert opinion derived from the medical literature, and on clinical experience. The recommended use of lower doses of glucocorticoids during surgical and medical stress should not de-emphasise the importance of additional supplementation during such events. Our recommendations do not replace clinical judgement, but their use will ensure that patients with AI are safely managed during illness or surgery without the risk of an adrenal crisis or excessive steroid dosing.