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1.
Clinics ; 68(12): 1537-1542, dez. 2013. graf
Article in English | LILACS | ID: lil-697707

ABSTRACT

OBJECTIVES: Estrogen has been shown to play an important protective role in non-reproductive systems, such as the cardiovascular system. Our aim was to observe gender differences in vivo with regard to the increase in macromolecular permeability and leukocyte-endothelium interaction induced by ischemia/reperfusion as well as in microvascular reactivity to vasoactive substances using the hamster cheek pouch preparation. METHODS: Thirty-six male and 36 female hamsters, 21 weeks old, were selected for this study, and their cheek pouches were prepared for intravital microscopy. An increase in the macromolecular permeability of post-capillary venules was quantified as a leakage of intravenously injected fluorescein-labeled dextran, and the leukocyte-endothelium interaction was measured as the number of fluorescent rolling leukocytes or leukocytes adherent to the venular wall, labeled with rhodamin G, during reperfusion after 30 min of local ischemia. For microvascular reactivity, the mean internal diameter of arterioles was evaluated after the topical application of different concentrations of two vasoconstrictors, phenylephrine (α1-agonist) and endothelin-1, and two vasodilators, acetylcholine (endothelial-dependent) and sodium nitroprusside (endothelial-independent). RESULTS: The increase in macromolecular permeability induced by ischemia/reperfusion was significantly lower in females compared with males [19 (17-22) leaks/cm2 vs. 124 (123-128) leaks/cm2, respectively, p<0.001), but the number of rolling or adherent leukocytes was not different between the groups. Phenylephrine-induced arteriolar constriction was significantly lower in females compared with males [77 (73-102)% vs. 64 (55-69)%, p<0.04], but there were no detectable differences in endothelin-1-dependent vasoreactivity. Additionally, arteriolar vasodilatation elicited by acetylcholine or sodium nitroprusside did not differ between the groups. CONCLUSION: The ...


Subject(s)
Animals , Cricetinae , Female , Male , Cardiovascular System/metabolism , Estrogens/metabolism , Microcirculation/physiology , Acetylcholine/pharmacology , Capillary Permeability , Cell Adhesion/physiology , Cheek/blood supply , Endothelium, Vascular/physiology , Leukocytes/physiology , Nitroprusside/pharmacology , Phenylephrine/pharmacology , Reperfusion Injury/metabolism , Sex Factors , Time Factors
2.
Clinics ; 66(11): 1961-1968, 2011. ilus, tab
Article in English | LILACS | ID: lil-605879

ABSTRACT

OBJECTIVE: Normal endothelial cells respond to shear stress by elongating and aligning in the direction of fluid flow. Hyperglycemia impairs this response and contributes to microvascular complications, which result in deleterious effects to the endothelium. This work aimed to evaluate cheek pouch microvessel morphological characteristics, reactivity, permeability, and expression of cytoskeleton and extracellular matrix components in hamsters after the induction of diabetes with streptozotocin. METHODS: Syrian golden hamsters (90-130 g) were injected with streptozotocin (50 mg/kg, i.p.) or vehicle either 6 (the diabetes mellitus 6 group) or 15 (the diabetes mellitus 15 group) days before the experiment. Vascular dimensions and density per area of vessels were determined by morphometric and stereological measurements. Changes in blood flow were measured in response to acetylcholine, and plasma extravasation was measured by the number of leakage sites. Actin, talin, α-smooth muscle actin, vimentin, type IV collagen, and laminin were detected by immunohistochemistry and assessed through a semiquantitative scoring system. RESULTS: There were no major alterations in the lumen, wall diameters, or densities of the examined vessels. Likewise, vascular reactivity and permeability were not altered by diabetes. The arterioles demonstrated increased immunoreactivity to vimentin and laminin in the diabetes mellitus 6 and diabetes mellitus 15 groups. DISCUSSION: Antibodies against laminin and vimentin inhibit branching morphogenesis in vitro. Therefore, laminin and vimentin participating in the structure of the focal adhesion may play a role in angiogenesis. CONCLUSIONS: Our results indicated the existence of changes related to cell-matrix interactions, which may contribute to the pathological remodeling that was already underway one week after induction of experimental diabetes.


Subject(s)
Animals , Cricetinae , Male , Diabetes Mellitus, Experimental/pathology , Laminin/ultrastructure , Vasodilator Agents/pharmacology , Vimentin/ultrastructure , Acetylcholine/pharmacology , Arterioles/drug effects , Arterioles/pathology , Cell Membrane Permeability/drug effects , Cheek/blood supply , Disease Models, Animal , Diabetes Mellitus, Experimental/chemically induced , Diabetes Mellitus, Experimental/metabolism , Histamine/pharmacology , Laminin/metabolism , Mesocricetus , Microvessels/drug effects , Microvessels/pathology , Random Allocation , Time Factors , Vimentin/metabolism
3.
Rev. bras. ecocardiogr ; 20(3): 12-21, jul.-set. 2007. tab, ilus, graf
Article in Portuguese | LILACS | ID: lil-485738

ABSTRACT

Fundamentos: A adesão das microesferas aos leucócitos no tecido inflamado tem sido discutida, porém, pouco se sabe sobre seu comportamento nos capilares. A avaliação dos efeitos circulatórios desse agente pode trazer informações sobre sua ação no miocárdio. Objetivo: Avaliar o comportamento microvascular e hemodinâmico das microesferas nos seguintes grupos: controle, isquemia-reperfusão, diabetes tipo 2, diabetes com isquemia e sepsis. Métodos: Experimentalmente estudou-se a microcirculação da bolsa da bochecha de 65 hamsters machos, sendo separados por grupos conforme a indução da doença de base G-1 igual isquemia/reperfusão. GD igual diabetes, GDI igual diabetes com isquemia GS igual sepsis em relação ao GC (grupo controle). Dentro de cada grupo avaliou-se a pressão arterial...


Subject(s)
Animals , Mice , Microspheres , Microcirculation/physiology , Rheology/methods , Diabetes Mellitus/classification , Diabetes Mellitus/diagnosis , Sepsis/complications
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