4 research outputs found

    Hemodialysis improves endothelial venous function in end-stage renal disease

    No full text
    The objective of the present study was to determine the acute effect of hemodialysis on endothelial venous function and oxidative stress. We studied 9 patients with end-stage renal disease (ESRD), 36.8 ± 3.0 years old, arterial pressure 133.8 ± 6.8/80.0 ± 5.0 mmHg, time on dialysis 55.0 ± 16.6 months, immediately before and after a hemodialysis session, and 10 healthy controls matched for age and gender. Endothelial function was assessed by the dorsal hand vein technique using graded local infusion of acetylcholine (endothelium-dependent venodilation, EDV) and sodium nitroprusside (endothelium-independent venodilation). Oxidative stress was evaluated by measuring protein oxidative damage (carbonyls) and antioxidant defense (total radical trapping antioxidant potential - TRAP) in blood samples. All patients were receiving recombinant human erythropoietin for at least 3 months and were not taking nitrates or a-receptor antagonists. EDV was significantly lower in ESRD patients before hemodialysis (65.6 ± 10.5) vs controls (109.6 ± 10.8; P = 0.010) and after hemodialysis (106.6 ± 15.7; P = 0.045). Endothelium-independent venodilation was similar in all comparisons performed. The hemodialysis session significantly decreased TRAP (402.0 ± 53.5 vs 157.1 ± 28.3 U Trolox/µL plasma; P = 0.001). There was no difference in protein damage comparing ESRD patients before and after hemodialysis. The magnitude of change in the EDV was correlated negatively with the magnitude of change in TRAP (r = -0.70; P = 0.037). These results suggest that a hemodialysis session improves endothelial venous function, in association with an antioxidant effect

    Effects of different frequencies of transcutaneous electrical nerve stimulation on venous vascular reactivity

    No full text
    Transcutaneous electrical nerve stimulation (TENS) is a type of therapy used primarily for analgesia, but also presents changes in the cardiovascular system responses; its effects are dependent upon application parameters. Alterations to the cardiovascular system suggest that TENS may modify venous vascular response. The objective of this study was to evaluate the effects of TENS at different frequencies (10 and 100 Hz) on venous vascular reactivity in healthy subjects. Twenty-nine healthy male volunteers were randomized into three groups: placebo (n=10), low-frequency TENS (10 Hz, n=9) and high-frequency TENS (100 Hz, n=10). TENS was applied for 30 min in the nervous plexus trajectory from the superior member (from cervical to dorsal region of the fist) at low (10 Hz/200 &#956;s) and high frequency (100 Hz/200 &#956;s) with its intensity adjusted below the motor threshold and intensified every 5 min, intending to avoid accommodation. Venous vascular reactivity in response to phenylephrine, acetylcholine (endothelium-dependent) and sodium nitroprusside (endothelium-independent) was assessed by the dorsal hand vein technique. The phenylephrine effective dose to achieve 70% vasoconstriction was reduced 53% (P<0.01) using low-frequency TENS (10 Hz), while in high-frequency stimulation (100 Hz), a 47% increased dose was needed (P<0.01). The endothelium-dependent (acetylcholine) and independent (sodium nitroprusside) responses were not modified by TENS, which modifies venous responsiveness, and increases the low-frequency sensitivity of &#945;1-adrenergic receptors and shows high-frequency opposite effects. These changes represent an important vascular effect caused by TENS with implications for hemodynamics, inflammation and analgesia

    Venous Endothelial Dysfunction In Chagas' Disease Patients Without Heart Failure [disfunção Endotelial Venosa Em Pacientes Com Doença De Chagas Sem Insuficiência Cardíaca]

    No full text
    OBJECTIVE: To analyze the venous endothelial function in Chagas' disease patients without heart failure. METHODS: The Chagas' disease Group (G1) was composed by 14 women and 2 men aged 46 ± 2,7 and the Control Group (G0) by 7 women and 1 man matched by age, weight and height. Dorsal Hand Vein Compliance Technique was used to evaluate the venous endothelial function. Crescent doses of phenylephrine were infused to get a 70% preconstriction of the vein; after that, acetylcholine and sodium nitroprusside were respectively administrated to analyze the endothelium-dependent and -independent venodilation. RESULTS: No significant systemic hemodynamic changes were observed in both groups during the experiment. The necessary phenylephrine dose to reach 70% preconstriction of the vein was significantly higher in the G1 (1116 ± 668,2 ng/ml) compared to G0 (103 ± 28 ng/ml) p = 0,05. The endothelium-dependent venous dilation was significantly lower in G1 (65,5 ± 8%) compared to G0 (137 ± 20 %) p = 0,009. No difference was observed in the endothelium-independent venous dilatation between groups. CONCLUSION: Patients with Chagas' disease without heart failure presented venous endothelial dysfunction.866466471Schmunis, G.A., American Trypanosomiasis as a public health problem (1994) Chagas' Disease and the Nervous System, pp. 3-29. , Pan American Health Organization (ed.). Washington, DC: Pan American OrganizationMarin-Neto, J.A., Simões, M.V., Sarabanda, A.V., Chagas'heart disease (1999) Arq Bras Cardiol, 72, pp. 247-280Mady, C., Barreto, A.C., Stolf, N., Lopes, E.A., Dauar, D., Wajngarten, M., Biopsia miocárdica na forma indeterminada da doença de Chagas (1981) Arq Bras Cardiol, 36, pp. 387-390Consolim-Colombo, F.M., Lopes, H.F., Rosetto, E.A., Endothelial function is preserved in Chagas' heart disease patients without heart failure (2004) Endothelium, 11 (5-6), pp. 241-246Guzman, Juan, C., Leon, Hernando, Casa, S., Juan, P., Disfunción autonómica y vascular en la fase asintomática de la enfermedad de Chagas (2004) Rev Colomb Cardiol, 11 (2), pp. 105-113Leiby, D.A., Rentas, F.J., Nelson, K.E., Evidence of Trypanosoma cruzi infection (Chagas' disease) among patients undergoing cardiac surgery (2000) Circulation, 102 (24), pp. 2978-2982Moncayo, A., Chagas disease: Current epidemiological trends after the interruption of vectorial and transfusional transmission in the Southern Cone countries (2003) Mem Inst Oswaldo Cruz, 5, pp. 577-591Ramos, S.G., Rossi, M.A., Microcirculation and Chagas' disease: Hypothesis and recent results (1999) Inst Med Trop São Paulo, 41 (2), pp. 123-129Soares Barreto-Filho, J.A., Consolim-Colombo, F.M., Ferreira Lopes, H., Martins Sobrinho, C.R., Guerra-Riccio, G.M., Krieger, E.M., Dysregulation of peripheral and central chemorefl ex responses in Chagas' heart disease patients without heart failure (2000) Circulation, 104 (15), pp. 1792-1798Rossi, M.A., Ramos, S.G., Coronary microvascular abnormalities in Chagas' disease (1996) Am Heart J, 132 (1), pp. 207-210Ianni, B.M., Arteaga, E., Frim, C.C., Pereira, C., Barreto, A.C., Mady, C., Chagas' heart disease: Evolutive evaluation of electrocardiographic and echocardiographic parameters in patients with the indeterminate form (2001) Arq Bras Cardiol, 77, pp. 59-62Consolim-Colombo, F.M., Filho, J.A., Lopes, H.F., Sobrinho, C.R., Otto, M.E., Riccio, G.M., Mady, C., Krieger, E.M., Decreased cardiopulmonary barorefl ex sensitivity in Chagas' heart disease (2000) Hypertension, 36 (6), pp. 1035-1039Anderson, T.J., Assessment and treatment of endothelial dysfunction in humans (1999) J Am Coll Cardiol, 34, pp. 631-638Drexler, H., Hornig, B., Endothelial dysfunction in human disease Endothelial dysfunction: A novel therapeutic target (1999) Mol Cell Cardiol, 31, pp. 51-60Schächinger, V., Britten, M.B., Zeiher, A.M., Prognostic impact of coronary vasodilator dysfunction on adverse long-term outcome of coronary heart disease (2000) Circulation, 101 (16), pp. 1899-1906Rossi, M.A., Aortic endothelial cell changes in the acute septicemic phase of experimental Trypanosoma cruzi infection in rats: Scanning and transmission electron microscopic study (1997) Am J Trop Med Hyg, 57 (3), pp. 321-327Camargos, E.R., Machado, C.R., Teixeira Jr., A.L., Rocha, L.L., Ferreira, A.J., Almeida, A.P., Barton, M., Teixeira, M.M., Role of endothelin during experimental Trypanosoma cruzi infection in rats (2002) Clin Sci, 103 (48 SUPPL.), pp. 64S-67S. , LondMorris, S.A., Tanowitz, H., Makman, M., Hatcher, V.B., Bilezikian, J.P., Trypanosoma cruzi: Alteration of cAMP metabolism following infection of human endothelial cell (1992) Exp Parasit, 74 (1), pp. 69-76Sunnemark, D., Frostegard, J., Orn, A., Harris, R.A., Cellular and cytokine characterization of vascular infl ammation in CBA/J mice chronically infected with Trypanosoma cruzi (1998) Scand J Immunol, 48 (5), pp. 480-484Tanowitz, H.B., Wittner, M., Morris, S.A., The putative mechanistic basis for the modulatory role of endothelin-1 in the altered vascular tone induced by Trypanosoma cruzi (1999) Endothelium, 6 (3), pp. 217-220Cardoni, R.L., Garcia, M.M., De Rissio, A.M., Proinfl ammatory and antiinflammatory cytokines in pregnant women chronically infected with Trypanosoma cruzi (2004) Acta Trop, 90 (1), pp. 65-72Ferreira, R.C., Ianni, B.M., Abel, L.C., Buck, P., Mady, C., Kalil, J., Cunha-Neto, E., Increased plasma levels of tumor necrosis factor-alpha in symptomatic "indeterminate" and Chagas disease cardiomyopathy patients (2003) Mem Inst Oswaldo Cruz, 98 (3), pp. 407-411Malvezi, A.D., Cecchini, R., De Souza, F., Tadokoro, C.E., Rizzo, L.V., Pinge-Filho, P., Involvement of nitric oxide (NO) and TNF-alpha in the oxidative stress associated with anemia in experimental Trypanosoma cruzi infection (2004) FEMS Immunol Med Microbiol, 41 (1), pp. 69-77Silva, J.S., Machado, F.S., Martins, G.A., The role of nitric oxide in the pathogenesis of Chagas disease (2003) Front Biosci, pp. s314-25Teichholz, L.E., Kreulen, T., Herman, M.V., Gorlin, R., Problems in echocardiographic volume determinations: Echocardiographic- angiographic correlation in the present or absence of a synergy (1976) Am J Cardiol, 37 (1), pp. 7-11Junqueira Jr., L.F., Discriminação entre as manifestações eletrocardiográficas normais, anormais e "borderline" na doença de Chagas (1992) Rev Soc Bras Med Trop, 25 (3 SUPPL.), p. 83Chalon, S., Bedarida, G.V., Moreno Jr., H., Tejura, B., Urae, A., Hoffman, B.B., Blaschke, T.F., Angiotensin-converting enzyme inhibition improves venous endothelial dysfunction in chronic smokers (1999) Clin Pharmacol Ther, 65, pp. 295-303Moreno Jr., H., Chalon, S., Urae, A., Tangphao, O., Abiose, A.K., Hoffman, B.B., Blaschke, T.F., Endothelial dysfunction in human hand veins is rapidly reversible after smoking cessation (1998) Am J Physiol, 275, pp. H1040-5Sousa, M.G., Yugar-Toledo, J.C., Rubira, M., Ascorbic acid improves impaired venous and arterial endothelium-dependent dilation in smokers (2005) Acta Pharmacol Sin, 26 (4), pp. 447-452Tangphao, O., Chalon, S., Moreno Jr., H., Hoffman, B.B., Blaschke, T.F., Pharmacokinetics of L-arginine during chronic administration to patients with hypercholesterolaemia (1999) Clin Sci, 96, pp. 199-207. , LondFurchgott, R.F., Zawadzki, J.V., The obligatory role of endothelial cells in the relaxation of arterial smooth muscle by acetylcholine (1980) Nature, 288, pp. 373-376Li, H., Forstermann, U., Nitric oxide in the pathogenesis of vascular disease (2000) J Pathol, 190, pp. 244-254Costa, P.C., Fortes, F.S., Machado, A.B., Sera from chronic chagasic patients depress cardiac electrogenesis and conduction (2000) Braz J Med Biol Res, 33 (4), pp. 439-446Masuda, M.O., Levin, M., De Oliveira, S.F., Functionally active cardiac antibodies in chronic Chagas' disease are specifically blocked by Trypanosoma cruzi antigens (1998) FASEB J, 12 (14), pp. 1551-1558Ogawa, S., Yoshikawa, T., Autoantibodies: Emerging upstream targets of arrhythmias and sudden death in patients with idiopathic dilated cardiomyopathy (2001) J Mol Cell Cardiol, 33 (10), pp. 1761-1763Pedrosa, R.C., (1998) Contribuição Ao Estudo Da Etiopatogenia Do Distúrbio de Condução e Da Eletrogênese Na Cardiopatia Chagásica Crônica: Efeitos de Anticorpos IgG de Pacientes Chagásicos Crônicos Na Eletrogênese e No Sistema de Condução Do Coração Isolado de Mamíferos, , Rio de Janeiro, Tese (Doutorado) - Universidade Federal do Rio de JaneiroSchulte, K.L., Laber, E., Meyer-Sabellek, W.A., Distler, A., Gotzen, R., Specific alpha-adrenoceptor-mediated vasoconstriction in human veins and interaction with the calcium entry blockers nifedipine and diltiazem (1985) J Hypertens (Suppl), pp. S239-41Simões, M.V., Pintya, A.O., Bromberg-Marin, G., Sarabanda, A.V., Antloga, C.M., Pazin-Filho, A., Maciel, B.C., Marin-Neto, J.A., Relation of regional sympathetic denervation and myocardial perfusion disturbance to wall motion impairment in Chagas' cardiomyopathy (2000) Am J Cardiol, 86 (9), pp. 975-981Davila, D.F., Bellabarba, G., Hernandez, L., Calmon, G., Torres, A., Donis, J.H., Barboza, J.S., Gonzalez, J.G., Plasma norepinephrine, myocardial damage and left ventricular systolic function in Chagas' heart disease (1995) Int J Cardiol, 24-52 (2), pp. 145-15

    Hemodialysis improves endothelial venous function in end-stage renal disease

    Get PDF
    The objective of the present study was to determine the acute effect of hemodialysis on endothelial venous function and oxidative stress. We studied 9 patients with end-stage renal disease (ESRD), 36.8 ± 3.0 years old, arterial pressure 133.8 ± 6.8/80.0 ± 5.0 mmHg, time on dialysis 55.0 ± 16.6 months, immediately before and after a hemodialysis session, and 10 healthy controls matched for age and gender. Endothelial function was assessed by the dorsal hand vein technique using graded local infusion of acetylcholine (endothelium-dependent venodilation, EDV) and sodium nitroprusside (endothelium-independent venodilation). Oxidative stress was evaluated by measuring protein oxidative damage (carbonyls) and antioxidant defense (total radical trapping antioxidant potential - TRAP) in blood samples. All patients were receiving recombinant human erythropoietin for at least 3 months and were not taking nitrates or α-receptor antagonists. EDV was significantly lower in ESRD patients before hemodialysis (65.6 ± 10.5) vs controls (109.6 ± 10.8; P = 0.010) and after hemodialysis (106.6 ± 15.7; P = 0.045). Endotheliumindependent venodilation was similar in all comparisons performed. The hemodialysis session significantly decreased TRAP(402.0 ± 53.5 vs 157.1 ± 28.3 U Trolox/μL plasma; P = 0.001). There was no difference in protein damage comparing ESRD patients before and after hemodialysis. The magnitude of change in the EDV was correlated negatively with the magnitude of change in TRAP (r = -0.70; P = 0.037). These results suggest that a hemodialysis session improves endothelial venous function, in association with an antioxidant effect
    corecore