RESUMEN
Rivaroxaban (RVX) was suggested to possess anti-inflammatory and vascular tone modulatory effects. The goal of this study was to investigate whether RVX impacts lipopolysaccharide (LPS)-induced acute vascular inflammatory response. Male rats were treated with 5 mg/kg RVX (oral gavage) followed by 10 mg/kg LPS i.p injection. Circulating levels of IL-6, MCP-1, VCAM-1, and ICAM-1 were measured in plasma 6 and 24 hours after LPS injection, while isolated aorta was used for gene expression analysis, immunohistochemistry, and vascular tone evaluation. RVX pre-treatment significantly reduced LPS mediated increase after 6h and 24h for IL-6 (4.4±2.2 and 2.8±1.7 fold), MCP-1 (1.4±1.5 and 1.3±1.4 fold) VCAM-1 (1.8±2.0 and 1.7±2.1 fold). A similar trend was observed in the aorta for iNOS (5.5±3.3 and 3.3±1.9 folds reduction, P<0.01 and P<0.001, respectively), VCAM-1 (1.3±1.2 and 1.4±1.3 fold reduction, P<0.05), and MCP-1 (3.9±2.2 and 1.9±1.6 fold reduction, P<0.01). Moreover, RVX pre-treatment, improved LPS-induced PE contractile dysfunction in aortic rings (Control vs LPS, Emax reduction = 35.4 and 31.19%, P<0.001; Control vs LPS+RVX, Emax reduction = 10.83 and 11.48%, P>0.05, respectively), resulting in 24.5% and 19.7% change in maximal constriction in LPS and LPS+RVX respectively. These data indicate that RVX pre-treatment attenuates LPS-induced acute vascular inflammation and contractile dysfunction.
Asunto(s)
Antiinflamatorios/administración & dosificación , Rivaroxabán/administración & dosificación , Vasculitis/tratamiento farmacológico , Vasoconstricción/efectos de los fármacos , Administración Oral , Animales , Aorta/efectos de los fármacos , Aorta/inmunología , Modelos Animales de Enfermedad , Endotelio Vascular/efectos de los fármacos , Endotelio Vascular/inmunología , Humanos , Lipopolisacáridos/inmunología , Masculino , Ratas , Vasculitis/sangre , Vasculitis/inmunología , Vasoconstricción/inmunologíaRESUMEN
Activation of the vascular endothelin-1 (ET-1) system is a key abnormality in vascular dysfunction of human obesity, especially in patients developing complications, such as the metabolic syndrome, diabetes, and atherosclerosis. Vascular insulin resistance, an increased insulin-stimulated endothelial production of ET-1 combined with impaired nitric oxide availability, is the hallmark of obesity-related vasculopathy, but dysregulated adipokine release from obese adipose tissue may contribute to the predominance of ET-1-dependent vasoconstriction. ET-1, in turn, might determine unhealthy obese adipose tissue expansion, with visceral and perivascular adipose tissue changes driving the release of inflammatory cytokines and atherogenic chemokines. In addition, ET-1 might also play a role in the development of the metabolic complications of obesity. Studies have shown inhibition of lipoprotein lipase activity by ET-1, with consequent hypertriglyceridemia. Also, ET-1 in pancreatic islets seems to contribute to beta cell dysfunction, hence affecting insulin production and development of diabetes. Moreover, ET-1 may play a role in nonalcoholic steatohepatitis. Recent clinical trials using innovative design have demonstrated that antagonism of ET-type A receptors protects against some complications of obesity and diabetes, such as nephropathy. These findings encourage further investigation to evaluate whether targeting the ET-1 system could afford better protection against other consequences of the obesity epidemic.
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Tejido Adiposo/metabolismo , Diabetes Mellitus Tipo 2/metabolismo , Nefropatías Diabéticas/metabolismo , Endotelina-1/metabolismo , Enfermedad del Hígado Graso no Alcohólico/metabolismo , Obesidad/complicaciones , Adipoquinas/metabolismo , Citocinas/metabolismo , Diabetes Mellitus Tipo 2/inmunología , Diabetes Mellitus Tipo 2/prevención & control , Nefropatías Diabéticas/inmunología , Nefropatías Diabéticas/prevención & control , Antagonistas de los Receptores de Endotelina/uso terapéutico , Endotelina-1/antagonistas & inhibidores , Endotelio Vascular/metabolismo , Humanos , Insulina/metabolismo , Resistencia a la Insulina/inmunología , Células Secretoras de Insulina/metabolismo , Enfermedad del Hígado Graso no Alcohólico/inmunología , Enfermedad del Hígado Graso no Alcohólico/prevención & control , Obesidad/inmunología , Obesidad/metabolismo , Receptor de Endotelina A/metabolismo , Vasoconstricción/efectos de los fármacos , Vasoconstricción/inmunologíaRESUMEN
Recurrent spontaneous vasospasm of the extracranial internal carotid artery (RSV-eICA) is a rarely recognized cause of ischemic stroke in young adults. However, its pathophysiology remains largely unknown. Through whole-exome sequencing of the ACOX3 gene of two dizygotic Korean twin brothers affected by RSV-eICA, we identified two compound heterozygous missense variants c.235 T > G (p.F79 V) and c.665G > A (p.G222E). In silico analysis indicated that both variants were classified as pathogenic. In vitro ACOX3 enzyme assay indicated practically no enzyme activity in both F79 V and G222E mutants. To determine the effect of the mutants on vasospasm, we used a collagen contraction assay on human aortic smooth muscle cells (HASMC). Carbachol, a cholinergic agonist, induces contraction of HASMC. Knockdown of ACOX3 in HASMC, using siRNA, significantly repressed HASMC contraction triggered by carbachol. The carbachol-induced HASMC contraction was restored by transfection with plasmids encoding siRNA-resistant wild-type ACOX3, but not by transfection with ACOX3 G222E or by co-transfection with ACOX3 F79 V and ACOX3 G222E, indicating that the two ACOX3 mutants suppress carbachol-induced HASMC contraction. We propose that an ACOX3 dysfunction elicits a prolonged loss of the basal aortic myogenic tone. As a result, smooth muscles of the ICA's intermediate segment, in which the sympathetic innervation is especially rich, becomes hypersensitive to sympathomimetic stimuli (e.g., heavy exercise) leading to a recurrent vasospasm. Therefore, ACOX3 dysfunction would be a causal mechanism of RSV-eICA. For the first time, we report the possible involvement of ACOX3 in maintaining the basal myogenic tone of human arterial smooth muscle.
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Acil-CoA Oxidasa/metabolismo , Arteria Carótida Interna/fisiopatología , Miocitos del Músculo Liso/metabolismo , Vasoconstricción/inmunología , Acil-CoA Oxidasa/genética , Humanos , Masculino , Músculo Liso/metabolismo , Músculo Liso/fisiopatología , Enfermedades Vasculares/etiologíaRESUMEN
INTRODUCTION: Flow-mediated dilation (FMD) quantifies endothelium-dependent vasomotor responses to short-term increases in blood flow. Low-flow mediated vasoconstriction (L-FMC) has been more recently introduced as additional measure of endothelial function, and its relationship with changes in blood flow, cardiovascular risk factors and FMD haâ§s been less well characterized. MATERIALS AND METHODS: We evaluated radial artery FMD and L-FMC along with the changes in blood flow and shear rate/stress in 584 patients with known or suspected coronary artery disease (72.9% men, mean age 67+/-11 years). Baseline blood flow and shear rate showed a modest association with radial artery FMD and L-FMC (R2â=â0.04 and R2â=â0.02, Pâ<â0.0001). Resting diameter showed a stronger association with FMD but not with L-FMC (R2â=â0.11, Pâ<â0.0001 and R2â=â0.005, Pâ=â0.09). Analysis with generalized additive models showed that age, sex and presence and extent of coronary artery disease were strongly related to both endothelial function measures (Pâ<â0.001 for both), but they explained only 12.4% and 10.1% of the variance in L-FMC and FMD. When the corresponding changes in blood flow were added to these statistical models, the % of variance explained raised to 20.4% and 17.7% for L-FMC and FMD. L-FMC was a strong predictor of FMD even after correction for the changes in blood flow. DISCUSSION: Changes in blood flow are the most important determinants of both L-FMC and FMD. These observations support the concept that both FMD and L-FMC measure endothelium-dependent, shear-induced, vasomotion.
Asunto(s)
Endotelio Vascular/fisiopatología , Vasoconstricción/inmunología , Anciano , Femenino , Humanos , Masculino , Persona de Mediana Edad , Flujo Sanguíneo Regional , Factores de Riesgo , Estrés MecánicoRESUMEN
Agonistic autoantibody to the angiotensin II type I receptor (AT1-AA) is highly associated with preeclampsia by increasing the sensitivity of Ang II during pregnancy in rats, thus leading to a preeclampsia-like syndrome. However, the mechanism underlying this phenomenon remains unclear. The purpose of this study was to observe AT1-AA amplification of Ang II-induced vasoconstriction in rat thoracic aortic rings. It was found that exposure to low concentrations of AT1-AA (0.4 nM) caused a contraction of <5% of the maximal response to 60 mM KCl. In addition, the Ang II-induced contractile response was amplified in the presence of a threshold contraction to AT1-AA, as manifested by a leftward shift of the midpoint of the concentration-response curve with no change in the maximal response. These results showed that preincubation with low AT1-AA could amplify the Ang II dose-response curve, and this amplification could be attenuated markedly by 0.1 µM heptapeptide AFHYESQ. In calcium-free Krebs solution, 10 µM of 2-aminoethoxydiphenyl borate (an IP3 receptor inhibitor) both blocked the AT1-AA base contraction and completely abolished the amplification. Both 5 µM of U-73122 (a phospholipase C inhibitor) and 10 µM of εV1-2 (an εPKC inhibitor) could partially inhibit the Ang II-induced contractile response. εV1-2, but not U-73122, could completely inhibit the amplification response of AT1-AA to Ang II. These results suggest that AT1-AA is able to cause amplification response to Ang II probably via the calcium-independent protein kinase C pathway, which may provide a new therapy strategy for preeclampsia.
Asunto(s)
Angiotensina II/administración & dosificación , Aorta Torácica/inmunología , Autoanticuerpos/inmunología , Músculo Liso Vascular/inmunología , Receptor de Angiotensina Tipo 1/inmunología , Vasoconstricción/inmunología , Animales , Aorta Torácica/efectos de los fármacos , Relación Dosis-Respuesta a Droga , Técnicas In Vitro , Contracción Muscular/efectos de los fármacos , Contracción Muscular/inmunología , Músculo Liso Vascular/efectos de los fármacos , Ratas , Ratas Wistar , Vasoconstricción/efectos de los fármacosRESUMEN
Activating autoantibodies to the angiotensin type 1 receptor (AT1R) are associated with hypertensive disorders. The angiotensin type 2 receptor (AT2R) is known to counter-regulate the actions of AT1R. We investigated whether AT2R autoantibodies produced in immunized rabbits will activate AT2R and suppress the vasopressor responses to angiotensin II and AT1R-activating autoantibodies. Five rabbits immunized with a peptide corresponding to the second extracellular loop of AT2R developed high AT2R antibody titers. Rabbit anti-AT2R sera failed to directly dilate isolated rat cremaster arterioles; however, when co-perfused with angiotensin II or AT1R-activating autoantibodies, the anti-AT2R sera significantly inhibited their contractile effects. Rabbit anti-AT2R sera recognized a predominant sequence near the N-terminus of the AT2R second extracellular loop. A decoy peptide based on this sequence effectively reversed the opposing effect of the anti-AT2R sera on angiotensin II-induced contraction of rat cremaster arterioles. A similar blockade of the anti-AT2R sera effect was observed with the AT2R antagonist PD 123319 and the guanylyl cyclase inhibitor 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one. Rabbit anti-AT2R sera reacted specifically with AT2R. No cross-reactivity with AT1R was observed. Blood pressure did not change in immunized animals. However, the pressor responses to incremental angiotensin II infusions were blunted in immunized animals. Thirteen subjects with primary aldosteronism demonstrated increased AT2R autoantibody levels compared with normal controls. In conclusion, AT2R autoantibodies produced in immunized rabbits have the ability to activate AT2R and counteract the AT1R-mediated vasoconstriction. These autoantibodies provide useful and selective tools for the study of their roles in blood pressure regulation and possible therapeutic intervention.
Asunto(s)
Angiotensina II/inmunología , Anticuerpos Bloqueadores/fisiología , Autoanticuerpos/inmunología , Hipertensión/inmunología , Receptor de Angiotensina Tipo 1/inmunología , Receptor de Angiotensina Tipo 2/inmunología , Vasoconstricción/inmunología , Animales , Arteriolas/efectos de los fármacos , Arteriolas/fisiopatología , Modelos Animales de Enfermedad , Ensayo de Inmunoadsorción Enzimática , Humanos , Hipertensión/tratamiento farmacológico , Hipertensión/fisiopatología , Masculino , Conejos , Ratas , Vasoconstricción/efectos de los fármacosRESUMEN
Autoimmune activities have been implicated in the pathogenesis of hypertension. High levels of autoantibodies against the second extracellular loop of α1-adrenoceptor (α1-AR autoantibody, α1-AA) are found in patients with hypertension, and α1-AA could exert a α1-AR agonist-like vasoconstrictive effect. However, whether the vasoconstrictive effect of α1-AA is enhanced in hypertension is unknown. Using aortic rings of spontaneously hypertensive rats (SHR) and normotensive Wistar-Kyoto (WKY) rats, we observed the vasoconstrictive responses to α1-AA with phenylephrine (α1-AR agonist) as a positive control drug. Aortic nitrotyrosine levels were also measured by ELISA and immunohistochemistry. The results showed that the aortic constrictive responses to α1-AA and phenylephrine (both 1 nmol L(-1)-10 µmol L(-1)) were greater in SHR than in WKY rats. Endothelial denudation or L-NAME (a non-selective NOS inhibitor) (100 µmol L(-1)) increased α1-AA- or phenylephrine-induced vasoconstrictions both in SHR and WKY. However, selective iNOS inhibitor 1400 W (10 µmol L(-1)) enhanced the α1-AA-induced aortic constriction in WKY, but not in SHR. The aortic nitrotyrosine level was significantly higher in SHR than WKY, as shown by both ELISA and immunohistochemistry. These results indicate that the vasoconstrictive response to α1-AA is enhanced in SHR, and this altered responsiveness is due to endothelial dysfunction and decreased NO bioavailability. The study suggests an important role of α1-AR autoimmunity in the pathogenesis and management of hypertension especially in those harboring high α1-AA levels.
Asunto(s)
Autoanticuerpos/inmunología , Hipertensión/inmunología , Receptores Adrenérgicos alfa 1/inmunología , Vasoconstricción/inmunología , Agonistas de Receptores Adrenérgicos alfa 1/farmacología , Animales , Aorta/inmunología , Aorta/metabolismo , Aorta/fisiopatología , Autoanticuerpos/metabolismo , Western Blotting , Relación Dosis-Respuesta a Droga , Endotelio Vascular/inmunología , Endotelio Vascular/fisiología , Inhibidores Enzimáticos/farmacología , Humanos , Hipertensión/metabolismo , Hipertensión/fisiopatología , Técnicas In Vitro , Masculino , NG-Nitroarginina Metil Éster/farmacología , Óxido Nítrico/metabolismo , Óxido Nítrico Sintasa/antagonistas & inhibidores , Óxido Nítrico Sintasa/metabolismo , Fenilefrina/farmacología , Ratas Endogámicas SHR , Ratas Endogámicas WKY , Ratas Wistar , Receptores Adrenérgicos alfa 1/fisiología , Tirosina/análogos & derivados , Tirosina/metabolismo , Vasoconstricción/efectos de los fármacos , Vasoconstrictores/farmacologíaRESUMEN
Obesity is a metabolic disorder of increasing prevalence worldwide and a risk factor for the development of insulin resistance (IR), metabolic syndrome and type 2 diabetes. Obesity is related to endothelial dysfunction through indirect mechanisms such as IR and the associated risk factors, and through direct mechanisms including the production of proinflammatory adipokines and elevated levels of free fatty acids (FFAs) by adipose tissue. Both clinical and experimental studies using genetic and diet-induced animal models of obesity have consistently shown impaired metabolic, agonistor flow-induced vasodilatations correlated with the amount of visceral adipose tissue and improved by dietary interventions and exercise. Compromised bioavailability of NO due to oxidative stress emerges as a main cause of endothelial dysfunction in obesity. Inflamed adipose tissue due to hypoxia, and in particular perivascular adipose tissue (PVAT), secrete larger amounts of reactive oxygen species (ROS) and adipokines that deteriorate NO signaling pathways. Abnormal production and activity of the vasoconstrictor/proatherogenic peptide endothelin-1 (ET-1) is also a hallmark of the obesity- associated endothelial dysfunction. Obesity, and in particular visceral obesity, is one of the main causes of IR, and the pathogenic factors that induce endothelial dysfunction in the earlier stages of obesity will further deteriorate the insulin signaling pathways in endothelial cells thus leading to blunted vasodilatation and abnormal capillary recruitment and substrate delivery by insulin to the target tissues. The present review is an attempt to summarize the current knowledge and the latest novel findings on the pathogenic mechanisms underlying endothelial dysfunction in obesity, in particular the local contribution of oxidative stress and inflammatory response from PVAT, and its role in the obesity-associated cardiovascular and metabolic complications.
Asunto(s)
Endotelio Vascular/fisiopatología , Resistencia a la Insulina , Obesidad/fisiopatología , Adipoquinas/inmunología , Diabetes Mellitus Tipo 2/etiología , Diabetes Mellitus Tipo 2/inmunología , Diabetes Mellitus Tipo 2/metabolismo , Endotelina-1/metabolismo , Endotelio Vascular/inmunología , Endotelio Vascular/metabolismo , Humanos , Resistencia a la Insulina/inmunología , Óxido Nítrico/metabolismo , Obesidad/inmunología , Obesidad/metabolismo , Estrés Oxidativo/inmunología , Estrés Oxidativo/fisiología , Especies Reactivas de Oxígeno/metabolismo , Factores de Riesgo , Vasoconstricción/inmunología , Vasoconstricción/fisiología , Vasodilatación/inmunología , Vasodilatación/fisiologíaRESUMEN
Central nervous system vasculitis is one of the foremost diagnostic challenges in rheumatology. It results in inflammation and destruction of the vasculature within the CNS. When vasculitis is confined to brain, meninges or spinal cord, it is referred to as primary angiitis of the CNS. Secondary CNS vasculitis occurs in the setting of a systemic vasculitis, auto-inflammatory or infectious disease. Prompt and accurate diagnosis of CNS vasculitis is essential to prevent irreversible brain damage, and to secure precise treatment decisions. Progressive debilitating and unexplained neurological deficits, associated with abnormal cerebrospinal fluid is the typical picture of the disease. Biopsy of the brain remains the gold standard diagnostic test. The differential diagnosis of CNS vasculitis is highly diverse with a broad array of mimics at the clinical, radiographic and angiographic levels.
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Encéfalo , Meninges , Médula Espinal , Vasculitis del Sistema Nervioso Central/clasificación , Vasculitis del Sistema Nervioso Central/diagnóstico , Encéfalo/inmunología , Encéfalo/metabolismo , Encéfalo/patología , Diagnóstico Diferencial , Cefalea/diagnóstico , Cefalea/inmunología , Cefalea/patología , Humanos , Incidencia , Inflamación/inmunología , Inflamación/metabolismo , Inflamación/patología , Meninges/inmunología , Meninges/metabolismo , Meninges/patología , Estudios Retrospectivos , Convulsiones/diagnóstico , Convulsiones/inmunología , Convulsiones/patología , Factores Sexuales , Médula Espinal/inmunología , Médula Espinal/metabolismo , Médula Espinal/patología , Hemorragia Subaracnoidea/diagnóstico , Hemorragia Subaracnoidea/inmunología , Hemorragia Subaracnoidea/patología , Vasculitis del Sistema Nervioso Central/inmunología , Vasoconstricción/inmunologíaRESUMEN
Caffeic acid phenethyl ester (CAPE) is the active component of honey bee propolis extracts. The results of the current study demonstrate that CAPE attenuated immunoglobulin (Ig)E-mediated allergic response in mast cells. Oral administration of CAPE inhibited IgE-mediated passive cutaneous anaphylaxis. CAPE effectively reduced both histamine and serotonin (5-HT)-induced vascular permeability in rats. CAPE also reduced histamine and leukotrienes (LTs) release from isolated rat peritoneal mast cells. Moreover, CAPE suppressed contraction induced by histamine (3 × 10(-8)-3 × 10(-5) M), 5-HT (3 × 10(-9)-10(-6) M) and adenosine (3 × 10(-8)-10(-5) M) in guinea pig tracheal zigzag. These findings provide evidence that CAPE may serve as an effective therapeutic agent for allergic diseases.
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Ácidos Cafeicos/farmacología , Hipersensibilidad/tratamiento farmacológico , Hipersensibilidad/inmunología , Inmunoglobulina E/inmunología , Alcohol Feniletílico/análogos & derivados , Adenosina/farmacología , Animales , Antialérgicos/inmunología , Antialérgicos/farmacología , Permeabilidad Capilar/efectos de los fármacos , Permeabilidad Capilar/inmunología , Cobayas , Histamina/inmunología , Liberación de Histamina/efectos de los fármacos , Liberación de Histamina/inmunología , Leucotrienos/inmunología , Masculino , Mastocitos/efectos de los fármacos , Mastocitos/inmunología , Anafilaxis Cutánea Pasiva/efectos de los fármacos , Anafilaxis Cutánea Pasiva/inmunología , Alcohol Feniletílico/farmacología , Ratas , Ratas Wistar , Serotonina/inmunología , Vasoconstricción/efectos de los fármacos , Vasoconstricción/inmunologíaRESUMEN
Increased vascular resistance in the fetoplacental circulation is a characteristic of preeclampsia. However, the potential molecular mechanisms of this condition remain obscure. The current study aimed to determine the direct effect of the peptide antigen corresponding to the second extracellular loop of the angiotensin II type 1 receptor (AT1R-EC(II) ) activating autoantibody (AT1-AA), a novel risk factor in preeclamptic patients, on fetoplacental villus stem blood vessels. Immunohistochemistry revealed that AT1 receptors were localized in the veins and arteries of human placental villi. Among 58 serum samples from preeclamptic patients, 28 (48.28%) were proved AT1-AA-positive by enzyme-linked immunosorbent assay [P<0.01 vs. 2/51 (3.92%) in the normal pregnancy group]. Total IgGs purified from AT1-AA-positive patients' sera (AT1-AA-IgGs) were added to isolated normal human placental blood vessels. The IgG significantly constricted both the villus veins and arteries in a dose-dependent manner in vitro, which could be blocked by the peptide corresponding to the human AT1R-EC(II) , anti-human IgG or the AT1 receptor antagonist losartan. Additionally, the venous constriction induced by AT1-AA-IgGs remained unchanged even at the end of the experiment (about half an hour), but the vasoconstriction caused by the AT1 receptor agonist angiotensin II underwent desensitization within three minutes. Collectively, our results demonstrated that AT1-AA in preeclamptic sera can directly constrict fetoplacental villus blood vessels without desensitization via the AT1 receptor in vitro, which might contribute to poor fetoplacental perfusion in preeclampsia.
Asunto(s)
Autoanticuerpos/efectos adversos , Circulación Placentaria/inmunología , Preeclampsia/metabolismo , Receptor de Angiotensina Tipo 1/inmunología , Vasoconstricción/inmunología , Adulto , Autoanticuerpos/sangre , Autoanticuerpos/inmunología , Femenino , Humanos , Inmunoglobulina G/sangre , Inmunoglobulina G/aislamiento & purificación , Placenta/irrigación sanguínea , Preeclampsia/inmunología , Embarazo , Receptor de Angiotensina Tipo 2/inmunología , Técnicas de Cultivo de Tejidos , Adulto JovenRESUMEN
OBJECTIVE: Hepatic venoconstriction plays a significant role in anaphylactic hypotension in anesthetized rats. The purpose of this study is to determine whether the primary site of anaphylactic venoconstriction in the liver venous circulation occurs prior to or distal to the sinusoidal capillaries. We also determined whether the hepatic blood volume is increased during anaphylactic hypotension. METHODS: We measured, using a servo-null micropipette pressure-measuring system, the hepatic venular transmural pressure (P micro hv) at the liver surface of anesthetized rats sensitized with the antigen of ovalbumin (1 mg). We also measured the liver lobe thickness, using the ultrasonic crystal dimension measuring system. Anaphylactic hypotension was induced by an intravenous injection of 0.6 mg ovalbumin. RESULTS: When the antigen was injected, the systemic arterial pressure decreased profoundly from 118+/-9 to 45+/-4 mm Hg, which was accompanied by an increase in Ppv and P micro hv: P micro hv only transiently increased from 3.1+/-0.9 to 8.8+/-1.5 cm H(2)O at 1 min and then rapidly returned to the baseline within 2 min, when Ppv continued to increase and reached the peak of 36+/-7 cm H(2)O at 3.5 min after antigen. This greater increase in Ppv-to-P micro hv gradient than that in P micro hv-to-Pcv gradient after antigen indicated that the constriction of the portal veins and the sinusoids much predominates over that of the hepatic veins. Along with this hepatic pre- and sinusoidal constriction, the liver lobe thickness significantly decreased by 4% after antigen. CONCLUSION: Pre-sinusoidal constriction during anaphylactic shock in anaesthetized rats increased the portal venous pressure while the hepatic venular pressure only increased slightly and transiently. This predominant pre-sinusoidal constriction is accompanied by a decrease in liver volume.
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Anafilaxia/fisiopatología , Presión Sanguínea/fisiología , Hipotensión/fisiopatología , Hígado/irrigación sanguínea , Anafilaxia/inducido químicamente , Anafilaxia/inmunología , Anestesia , Animales , Antígenos/efectos adversos , Antígenos/inmunología , Volumen Sanguíneo/efectos de los fármacos , Venas Hepáticas/efectos de los fármacos , Venas Hepáticas/inmunología , Hipotensión/inducido químicamente , Hipotensión/inmunología , Hígado/efectos de los fármacos , Hígado/inmunología , Circulación Hepática/efectos de los fármacos , Circulación Hepática/inmunología , Masculino , Tamaño de los Órganos/efectos de los fármacos , Tamaño de los Órganos/inmunología , Ovalbúmina/inmunología , Ovalbúmina/farmacología , Presión Portal/efectos de los fármacos , Vena Porta/efectos de los fármacos , Vena Porta/inmunología , Ratas , Ratas Sprague-Dawley , Factores de Tiempo , Vasoconstricción/efectos de los fármacos , Vasoconstricción/inmunología , Venas/efectos de los fármacos , Venas/inmunología , Presión Venosa/efectos de los fármacosRESUMEN
Obstructive sleep apnea (OSA) is a highly prevalent sleep disorder leading to cardiovascular and metabolic complications. OSA is also a multicomponent disorder, with intermittent hypoxia (IH) as the main trigger for the associated cardiovascular and metabolic alterations. Indeed, recurrent pharyngeal collapses during sleep lead to repetitive sequences of hypoxia-reoxygenation. This IH induces several consequences such as hemodynamic, hormonometabolic, oxidative, and immuno-inflammatory alterations that may interact and aggravate each other, resulting in artery changes, from adaptive to degenerative atherosclerotic remodeling. Atherosclerosis has been found in OSA patients free of other cardiovascular risk factors and is related to the severity of nocturnal hypoxia. Early stages of artery alteration, including functional and structural changes, have been evidenced in both OSA patients and rodents experimentally exposed to IH. Impaired vasoreactivity with endothelial dysfunction and/or increased vasoconstrictive responses due to sympathetic, endothelin, and renin-angiotensin systems have been reported and also contribute to vascular remodeling and inflammation. Oxidative stress, inflammation, and vascular remodeling can be directly triggered by IH, further aggravated by the OSA-associated hormonometabolic alterations, such as insulin resistance, dyslipidemia, and adipokine imbalance. As shown in OSA patients and in the animal model, genetic susceptibility, comorbidities (obesity), and life habits (high fat diet) may aggravate atherosclerosis development or progression. The intimate molecular mechanisms are still largely unknown, and their understanding may contribute to delineate new targets for prevention strategies and/or development of new treatment of OSA-related atherosclerosis, especially in patients at risk for cardiovascular disease.
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Aterosclerosis/inmunología , Apnea Obstructiva del Sueño/inmunología , Adipoquinas/sangre , Adipoquinas/inmunología , Animales , Aterosclerosis/sangre , Aterosclerosis/etiología , Aterosclerosis/genética , Dislipidemias/sangre , Dislipidemias/inmunología , Endotelio Vascular/inmunología , Endotelio Vascular/metabolismo , Humanos , Hipoxia/complicaciones , Hipoxia/genética , Hipoxia/inmunología , Inflamación , Resistencia a la Insulina/inmunología , Oxidación-Reducción , Sistema Renina-Angiotensina/inmunología , Apnea Obstructiva del Sueño/sangre , Apnea Obstructiva del Sueño/complicaciones , Apnea Obstructiva del Sueño/genética , Vasoconstricción/inmunologíaRESUMEN
The most dangerous and life-threatening manifestation of allergic diseases is anaphylaxis, a condition in which the cardiovascular system is responsible for the majority of clinical symptoms and for potentially fatal outcome. The heart is both a source and a target of chemical mediators released during allergic reactions. Mast cells are abundant in the human heart, where they are located predominantly around the adventitia of large coronary arteries and in close contact with the small intramural vessels. Cardiac mast cells can be activated by a variety of stimuli including allergens, complement factors, general anesthetics and muscle relaxants. Mediators released from immunologically activated human heart mast cells strongly influence ventricular function, cardiac rhythm and coronary artery tone. Histamine, cysteinyl leukotrienes and platelet-activating factor (PAF) exert negative inotropic effects and induce myocardial depression that contribute significantly to the pathogenesis of anaphylactic shock. Moreover, cardiac mast cells release chymase and renin that activates the angiotensin system locally, which further induces arteriolar vasoconstriction. The number and density of cardiac mast cells is increased in patients with ischaemic heart disease and dilated cardiomyopathies. This observation may help explain why these conditions are major risk factors for fatal anaphylaxis. A better understanding of the mechanisms involved in cardiac mast cell activation may lead to an improvement in prevention and treatment of systemic anaphylaxis.
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Sistema Cardiovascular/inmunología , Hipersensibilidad/inmunología , Mastocitos/inmunología , Miocardio/inmunología , Anafilaxia/inmunología , Animales , Arterias/inmunología , Sistema Cardiovascular/fisiopatología , Humanos , Factores Inmunológicos/inmunología , Contracción Miocárdica/inmunología , Vasoconstricción/inmunologíaRESUMEN
Preeclampsia is a serious pathologic complication during pregnancy, and its pathogenesis remains poorly understood. Recent studies have demonstrated that autoantibodies against angiotensin II type 1A receptor (AT1-AA) are present in women with preeclampsia. However, their role in the development of hypertension in preeclamptic patients has never been previously investigated. The present study was designed to determine whether AT1-AA isolated from the sera of preeclamptic patients causes vascular constriction and, if so, to further investigate the cellular receptors that mediate their vasoactivity. Blood samples were collected from 49 pregnant women (preeclampsia = 31, control = 18) and AT1-AA was detected using enzyme-linked immunosorbent assay. Vasoconstrictive effect of purified IgG from the sera of either preeclamptic patients or normal pregnant women was determined in isolated rat thoracic aorta, arteriae cerebri media and coronary artery. Compared with normal pregnant women, frequency of AT1-AA positive samples was markedly increased in preeclamptic patients (80.7 vs. 5.6%, P < 0.01). In isolated thoracic aortic rings, middle cerebral artery and coronary artery segments, AT1-AA induced vasoconstriction in a concentration-dependent fashion (P < 0.01). The vasoconstrictive effect of AT1-AA was completely blocked by losartan, an AT1-receptor antagonist. These data demonstrate that the AT1-AA causes significant vascular constriction in large conduit vessel as well as small resistant vessels though activation of the AT1 receptor. These results suggest that overproduction of AT1-AA is a novel risk factor in pregnant women and may play a causative role in the development of hypertension and vascular injury in preeclamptic patients.
Asunto(s)
Autoanticuerpos/sangre , Hipertensión/inmunología , Preeclampsia/inmunología , Receptor de Angiotensina Tipo 1/inmunología , Vasoconstricción/inmunología , Adulto , Bloqueadores del Receptor Tipo 1 de Angiotensina II/farmacología , Animales , Aorta Torácica/efectos de los fármacos , Aorta Torácica/inmunología , Autoanticuerpos/farmacología , Relación Dosis-Respuesta Inmunológica , Femenino , Humanos , Hipertensión/epidemiología , Inmunoglobulina G/sangre , Inmunoglobulina G/farmacología , Técnicas In Vitro , Losartán/farmacología , Masculino , Preeclampsia/epidemiología , Embarazo , Ratas , Ratas Wistar , Receptor de Angiotensina Tipo 1/metabolismo , Factores de Riesgo , Vasoconstricción/efectos de los fármacosRESUMEN
Activation of PAR-2 in the vasculature affects vascular tone and adhesion of leukocytes to the endothelium. Since adhesion of leukocytes is increased following vascular injury and is important in determining the extent of neointima formation, we hypothesised that mice lacking PAR-2 may have reduced neointima formation following vascular injury. PAR-2 activating peptides and trypsin induced endothelium-dependent relaxation of mouse carotid artery which was absent in the knockout mouse. Lack of a PAR-2 receptor did not affect lymphocyte adhesion under basal conditions, but reduced the contractile response produced by lymphocytes. Twenty-eight days after denuding injury, vessel contraction to lymphocytes was reduced in both strains while lymphocyte adhesion was significantly greater in PAR-2(+/+) mice compared to the PAR-2 knockout mice. Neointimal area was markedly reduced in the PAR-2 knockout mouse. Our data show that PAR-2 modulates inflammatory cell adhesion when stimulated and in mice lacking the PAR-2 receptor, adhesion to injured vessels is reduced with a consequent reduction in neointima formation.
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Traumatismos de las Arterias Carótidas/inmunología , Traumatismos de las Arterias Carótidas/metabolismo , Linfocitos/patología , Receptor PAR-2/inmunología , Vasculitis/metabolismo , Animales , Aorta Torácica/inmunología , Aorta Torácica/lesiones , Aorta Torácica/metabolismo , Arteria Carótida Común/inmunología , Arteria Carótida Común/metabolismo , Adhesión Celular/inmunología , Femenino , Masculino , Ratones , Ratones Noqueados , Receptor PAR-2/genética , Receptor PAR-2/metabolismo , Túnica Íntima/inmunología , Túnica Íntima/metabolismo , Túnica Íntima/patología , Vasculitis/inmunología , Vasoconstricción/inmunología , Vasodilatación/inmunologíaRESUMEN
Agonists of cellular receptors, such as receptor tyrosine kinases, G protein-coupled receptors, cytokine receptors, etc., activate phospholipases (C(gamma), C(beta), A(2), D), sphingomyelinase, and phosphatidylinositol-3-kinase. This produces active lipid metabolites, some of which are second messengers: inositol trisphosphate, diacylglycerides, ceramide, and phosphatidylinositol 3,4,5-trisphosphate. These universal mechanisms are involved in signal transduction to maintain blood vessel functions: regulation of vasodilation and vasoconstriction, mechanical stress resistance, and anticoagulant properties of the vessel lumen surface. Different signaling pathways realized through lipid second messengers interact to one another and modulate intracellular events. In early stages of atherogenesis, namely, accumulation of low density lipoproteins in the vascular wall, cascades of pro-atherogenic signal transduction are triggered through lipid second messengers. This leads to atherosclerosis, the general immuno-inflammatory disease of the vascular system.
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Aterosclerosis/metabolismo , Metabolismo de los Lípidos , Lípidos , Músculo Liso Vascular/metabolismo , Sistemas de Mensajero Secundario , Animales , Aterosclerosis/inmunología , Humanos , Inflamación/inmunología , Inflamación/metabolismo , Lipasa/inmunología , Lipasa/metabolismo , Metabolismo de los Lípidos/inmunología , Lípidos/inmunología , Músculo Liso Vascular/inmunología , Fosfatidilinositol 3-Quinasas/inmunología , Fosfatidilinositol 3-Quinasas/metabolismo , Receptores de Superficie Celular/inmunología , Receptores de Superficie Celular/metabolismo , Sistemas de Mensajero Secundario/inmunología , Esfingomielina Fosfodiesterasa/inmunología , Esfingomielina Fosfodiesterasa/metabolismo , Estrés Mecánico , Resistencia Vascular/inmunología , Vasoconstricción/inmunología , Vasodilatación/inmunologíaRESUMEN
BACKGROUND: Saphenous veins are often used for coronary artery bypass grafting (CABG), but loss of patency is a problem. The surgical procedure may contribute to graft injury. Our aim was to study the impact of surgical handling of saphenous veins on graft inflammation and vascular function. METHODS: Biopsy samples of saphenous veins were taken from 9 patients undergoing elective CABG at the start of vein harvesting (open technique) and after the last proximal anastomosis was sutured. Messenger RNA was extracted and amplified with semiquantitative reverse transcription polymerase chain reaction. Gene expression of proinflammatory cytokines (tumor necrosis factor-alpha, interleukin-1beta), leukocyte adhesion molecules (E-selectin, intercellular adhesion molecule-1), and vasoactive substances (endothelin-1, inducible and endothelial nitric oxide synthase) was investigated. Translocation of nuclear factor-kappaB (NFkappaB) was evaluated with electrophoretic mobility shift assay. Immunostaining for von Willebrand factor was performed to evaluate loss of endothelium, and in vitro vein reactivity to phenylephrine and endothelin-1 was studied. RESULTS: Gene expression of cytokines and leukocyte adhesion molecules increased after graft harvesting and storage, whereas vasoactive substances did not change. Nuclear translocation of NFkappaB occurred after surgical handling, concurrent with partial loss of endothelium and impaired contractile function. CONCLUSIONS: Standard surgical handling of vein grafts induces NFkappaB-driven inflammation in the vessel wall and impairs vascular function. This may potentially contribute to both early and late graft occlusion.
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Inflamación/inmunología , Vena Safena/inmunología , Vena Safena/cirugía , Recolección de Tejidos y Órganos/efectos adversos , Biopsia , Moléculas de Adhesión Celular/inmunología , Puente de Arteria Coronaria/métodos , Citocinas/inmunología , Femenino , Expresión Génica/inmunología , Oclusión de Injerto Vascular/inmunología , Humanos , Masculino , Persona de Mediana Edad , FN-kappa B/inmunología , Óxido Nítrico Sintasa de Tipo III/inmunología , Vena Safena/patología , Grado de Desobstrucción Vascular/inmunología , Vasoconstricción/inmunología , Vasodilatación/inmunologíaRESUMEN
Effects of hematocrit (Hct) on N-nitro-L-arginine methyl ester (L-NAME)-induced modulation of anaphylactic venoconstriction were determined in isolated perfused rat livers. The rats were sensitized with ovalbumin (1 mg), and the livers were excised 2 weeks later and perfused portally and recirculatingly under constant flow at Hct of 0%, 5%, 16%, and 22%. The hepatic sinusoidal pressure was estimated via the double occlusion pressure (Pdo), and the presinusoidal resistance (Rpre) and the postsinusoidal resistance (Rhv) were calculated. The antigen of ovalbumin 0.1 mg was injected into the reservoir at 10 minutes after pretreatment with L-NAME (100 microM) or D-NAME (100 microM). Perfusate viscosity, a determinant of vascular resistance and shear stress, was increased in parallel with Hct. In the D-NAME groups, antigen caused predominant presinusoidal constriction. The magnitude of venoconstriction was significantly smaller at Hct 0% than at Hct 5% to 22%, whereas no significant differences were found among Hct 5% to 22%. L-NAME potentiated the antigen-induced increase in Rpre, but not in Rpost at Hct 5% to 22% as compared with D-NAME. But the augmentative effects of L-NAME were similar in magnitude among Hct 5% to 22%. These findings suggest that hepatic anaphylaxis increases production of nitric oxide, which consequently attenuates anaphylactic presinusoidal constriction in rat livers, and that these effects are independent of perfusate Hct or viscosity in blood-perfused rat livers.
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Anafilaxia/fisiopatología , Hematócrito , Circulación Hepática/efectos de los fármacos , NG-Nitroarginina Metil Éster/farmacología , Anafilaxia/inducido químicamente , Anafilaxia/inmunología , Animales , Sinergismo Farmacológico , Inhibidores Enzimáticos/química , Inhibidores Enzimáticos/farmacología , Hígado/irrigación sanguínea , Hígado/efectos de los fármacos , Hígado/metabolismo , Hígado/fisiopatología , Masculino , NG-Nitroarginina Metil Éster/química , Ovalbúmina/administración & dosificación , Ovalbúmina/inmunología , Perfusión/métodos , Presión Portal/efectos de los fármacos , Ratas , Ratas Sprague-Dawley , Estereoisomerismo , Resistencia Vascular/efectos de los fármacos , Vasoconstricción/efectos de los fármacos , Vasoconstricción/inmunología , ViscosidadRESUMEN
The present study investigated whether sympathetic neurotransmission is altered at an early stage of diabetes in mesenteric small arteries isolated from female non-obese diabetic (NOD) and control animals without diabetes from the same mouse strain. The NOD diabetic mice had increased plasma glucose and hypertension. Confocal microscopy showed distribution of nerve terminals was similar, but immunoreaction intensity for neuropeptide Y (NPY) and tyrosine hydroxylase was higher in small arteries from NOD diabetic compared with NOD control mice. In the presence of prazosin and activated with vasopressin, electrical field stimulation evoked contractions which were more pronounced in mesenteric arteries from NOD diabetic versus NOD control mice and inhibited by the NPY Y(1) receptor antagonist, BIBP 3226. NPY concentration-response curves were leftward shifted in arteries from NOD diabetic versus NOD control both in arteries with and without endothelium, but not in the presence of the BIBP 3226. The present findings suggest that enhanced NPY content and vasoconstriction to NPY by activation of NPY Y(1) receptors in arteries from diabetic mice may contribute to the enhanced sympathetic nerve activity and vascular resistance in female non-obese early diabetic animals.