Brazilian Journal of Anesthesiology
https://bjan-sba.org/article/doi/10.1590/S0034-70942003000600008
Brazilian Journal of Anesthesiology
Scientific Article

Efeitos do halotano, isoflurano e sevoflurano sobre a função renal em cães sob pinçamento aórtico infra-renal

Effects of halothane, isoflurane and sevoflurane on renal function in dogs under infra-renal aortic cross-clamping

Flora Margarida Barra Bisinotto; José Reinaldo Cerqueira Braz

Downloads: 0
Views: 968

Resumo

JUSTIFICATIVA E OBJETIVOS: O pinçamento infra-renal da aorta abdominal pode produzir alterações renais. O objetivo do estudo foi avaliar os efeitos do halotano, isoflurano e sevoflurano sobre a função renal, em cães submetidos a pinçamento aórtico infra-renal. MÉTODO: O estudo aleatório foi realizado em 30 cães, distribuídos em três grupos, de acordo com o anestésico halogenado utilizado durante a anestesia, em concentrações equipotentes de 0,75 CAM: GH (n = 10) - halotano a 0,67%; GI (n = 10) - isoflurano a 0,96%; e GS (n = 10) - sevoflurano a 1,8%. Em todos os animais foi realizada ligadura infra-renal da aorta, por período de 30 minutos. Os atributos renais foram estudados nos momentos: C (controle), após 15 (Ao15) e 30 (Ao30) minutos de pinçamento aórtico, e após 15 (DAo15) e 30 (DAo30) minutos do despinçamento aórtico. RESULTADOS: A depuração de água livre foi menor nos grupos GI e GS, em relação ao GH, após o despinçamento aórtico (p < 0,05). Durante o pinçamento aórtico, nos três grupos, houve aumento do débito urinário, da excreção urinária de sódio e da depuração de sódio, e diminuição da osmolaridade urinária (p < 0,05). A resistência vascular renal e a fração de filtração aumentaram somente em GS (p < 0,05), enquanto a excreção fracionária de sódio aumentou em GH e GI (p < 0,05). Após o despinçamento aórtico, houve normalização dos atributos que haviam se alterado, com exceção da osmolaridade urinária, que continuou em níveis menores do que os do controle em todos os grupos (p < 0,05). A resistência vascular renal e a fração de filtração continuaram mais elevadas em GS, acompanhadas por diminuição do fluxo sangüíneo renal e da depuração de para-aminohipurato de sódio (p < 0,05). CONCLUSÕES: No cão nas condições experimentais empregadas, a inalação de halotano e isoflurano a 0,75 CAM, mas não de sevoflurano, atenuou a principal alteração após o pinçamento infra-renal da aorta, que é o aumento da resistência vascular renal.

Palavras-chave

ANESTÉSICOS, ANESTÉSICOS, ANESTÉSICOS, ANESTÉSICOS, ANIMAL, CIRURGIA, CIRURGIA

Abstract

BACKGROUND AND OBJECTIVES: Infra-renal aortic cross-clamping is associated to renal effects. This study aimed at analyzing halothane, isoflurane and sevoflurane effects on renal function of dogs submitted to infra-renal aortic cross-clamping. METHODS: This study involved 30 mixed-breed dogs randomly distributed in three groups, according to equipotent anesthetic doses (0.75 MAC) of inhaled anesthetics: GH (n = 10) - 0.67% halothane; GI (n = 10) - 0.96% isoflurane; and GS (n = 10) - 1.8% sevoflurane. All animals were submitted to infra-renal aortic cross-clamping for 30 minutes. Renal parameters were evaluated at control (C), 15 (Ao15) and (Ao30) minutes after aortic cross-clamping, and 15 (DAo15) and 30 (DAo30) minutes after aortic unclamping. RESULTS: Free water clearance was significantly lower in GI and GS as compared to GH (p < 0.05) after aortic unclamping. Urinary output, sodium urinary excretion and sodium clearance have significantly increased during aortic cross-clamping, while urinary osmolarity has decreased in all groups (p < 0.05). Renal vascular resistance and filtration fraction have increased during aortic cross-clamping in GS only, while sodium fractional excretion increased in GH and GI (p < 0.05). All renal parameters had returned to control levels after aortic unclamping, with the exception of urinary osmolality which has remained below control levels in all groups (p < 0.05). Renal vascular resistance and filtration fraction have remained higher in GS, followed by renal blood flow and PAH clearance decrease (p < 0.05). CONCLUSIONS: In dogs under our experimental conditions, 0.75 MAC of halothane or isoflurane, but not 0.75 MAC of sevoflurane, have minimized renal vascular resistance increase, which is the major infra-renal aortic cross-clamping effect.

Keywords

ANESTHETICS, ANESTHETICS, ANESTHETICS, ANESTHETICS, ANIMAL, SURGERY, SURGERY

References

McCombs PR, Roberts B. Acute renal failure following resection of abdominal aortic aneurysm. Surg Gynecol Obstet. 1979;148:175-178.

Aronson S, Blumenthal R. Perioperative renal dysfunction and cardiovascular anesthesia: concerns and controversies. J Cardiothor Vasc Anesth. 1998;12:567-586.

Youngberg JA. Anesthetic Considerations for Major Vascular Surgery. 1994:511.

Gamulin Z, Forster A, Morel D. Effects of infrarenal aortic cross-clamping on renal haemodynamics in humans. Anesthesiology. 1984;61:394-399.

Awad RW, Barham WJ, Taylor DN. The effect of infra-renal aortic reconstruction on glomerular filtration rate and effective renal plasma flow. Eur J Vasc Surg. 1992;6:362-367.

Abbot WM, Austen WG. The reversal of renal cortical ischemia during aortic occlusion by mannitol. J Surg Res. 1974;16:482-489.

Paul MD, Mazer CD, Byrick RJ. Influence of mannitol and dopamine on renal function during elective infrarenal aortic clamping in man. Am J Nephrol. 1986;6:427-434.

Colson P, Capdevilla X, Balert H. Effects of halothane and isoflurane on transient renal dysfunction associated with infrarenal aortic cross-clamping. J Cardiothor Vasc Anesth. 1992;6:295-298.

Gelman S. The pathophysiology of aortic cross-clamping and unclamping. Anesthesiology. 1995;82:1026-1060.

Alpert RA, Roizen MF, Hamilton WK. Intraoperative urinary output does not predict postoperative renal function in patients undergoing abdominal aortic revascularization. Surgery. 1984;95:707-711.

Colson P, Capdevilla X, Cuchet D et al. Does choice of the anesthetic influence renal function during infrarenal aortic surgery?. Anesth Analg. 1992;74:481-485.

Colson P, Ribsteien J, Séguin JR. Mechanism of renal hemodynamic impairment during infrarenal aortic cross-clamping. Anesth Analg. 1992;75:18-23.

Higuchi H, Arimura S, Sumiura H et al. Urine concentrating ability after prolonged sevoflurane anesthesia. Br J Anaesth. 1994;73:239-240.

Mazze RI, Callan CM, Galvez ST. The effects of sevoflurane on serum creatinine and blood urea nitrogen concentrations: A retrospective, twenty-two-center, comparative evaluation of renal function in adult surgical patients. Anesth Analg. 2000;90:683-688.

Cook TL, Beppu WJ, Hitt BA et al. A comparison of renal effects and metabolism of sevoflurane and methoxyflurane in enzyme induced rats. Anesth Analg. 1975;54:829-834.

Malan TP, Kadota Y, Mota H. Renal function after sevoflurane or enflurane anesthesia in the Fischer 344 rat. Anesth Analg. 1993;77:817-821.

Jin L, Baillie TA, Davis MR. Nephrotoxicity of sevoflurane compound A [fluoromethyl -2,2-difluoro-1 (trifluoro methyl) vinyl ether] in rats: evidence for glutathione and cysteine conjugate formation and the role of renal cysteine conjugate beta-lipase. Biochemical Biophysical Research Communications. 1995;210:498-506.

Kharasch ED, Hoffman GM, Thorning D et al. Role of renal cysteine conjugate beta-lyase pathway in inhaled compound A nephrotoxicity in rats. Anesthesiology. 1998;88:1624-1633.

Frink EJ, Isner RJ, Malan TP. Sevoflurane degradation product concentrations with soda lime during prolonged anesthesia. J Clin Anesth. 1994;74:241-245.

Eger II EI, Kobliun DD, Bowland T. Nephrotoxicity of sevoflurane versus desflurane anesthesia in volunteers. Anesth Analg. 1997;84:160-168.

Higuchi H, Sumita S, Wada H et al. Effects of sevoflurane and isoflurane on renal function and on possible markers of nephrotoxicity. Anesthesiology. 1998;89:307-322.

Groudine SB, Fragen RJ, Kharasch ED et al. Comparison of renal function following anesthesia with low-flow sevoflurane and isoflurane. J Clin Anesth. 1999;11:201-207.

Cozen FC, Kharasch ED, Czerner FA et al. Low-flow sevoflurane compared with low-flow isoflurane anesthesia in patients with stable renal insufficiency. Anesthesiology. 2002;97:578-584.

Higuchi H, Adachi Y, Wada H et al. The effects of low-flow sevoflurane and isoflurane anesthesia on renal function in patients with stable moderate renal insufficiency. Anesth Analg. 2001;92:650-655.

Kazama T, Ikeda K. Comparison of MAC and the rate of rise of alveolar concentration of sevoflurane with halothane and isoflurane in the dog. Anesthesiology. 1988;68:435-437.

Morrison DF. Multivariate Statistical Methods. 1967:338.

Roisen MF, Beaupre PN, Alpert RA. Monitoring with two-dimensional transesophageal echocardiography: Comparison of myocardial function in patients undergoing supra-celiac, suprarenal-infraceliac, or infra-renal aortic occlusion. J Vasc Surg. 1984;1:300-305.

Harpole DH, Clements FM, Quill T. Right and left ventricular performance during and after abdominal aortic aneurysm repair. Ann Surg. 1989;209:356-362.

Quintin L, Bonnet F, Macquin I. Aortic surgery: effect of clonidine on intra-operative catecholaminergic and circulatory stability. Acta Anaesthesiol Scand. 1990;34:132-137.

Seeman-Lodding H, Biber B, Martner J. Cardiovascular responses to experimental infra-renal aortic cross-clamping: Modulating effects of isoflurane, sodium nitroprussiate and milrinone. Acta Anaesthesiol Scand. 1996;40:408-415.

Kien ND, White DA, Reitan JA. The influence of adenosine triphosphate on left ventricular function and blood flow distribution during aortic cross-clamping in dogs. J Cardiothor Vasc Anesth. 1987;1:114-122.

Sato JK. Estudo das repercussões hemodinâmicas e renais do pinçamento aórtico infra-renal no cão: Efeitos do pré-tratamento com isradipina. :110.

Cronenwett JL, Lindenauer SM. Distribution of intrarenal blood flow following aortic clamping and declamping. J Surg Res. 1977;22:469-482.

Roberts AJ, Nora JD, Hughes WA. Cardiac and renal responses to cross-clamping of the descending thoracic aorta. J Thorac Cardiovasc Surg. 1983;86:732-741.

Malnic G. Curso Prático. Fisiologia Renal. 1986:369-390.

Rahman SN, Batt AT, Dubose TD. Differentiating clinical effects of ANP in oliguric and non-oliguric ATN. J Am Soc Nephrol. 1995;6:474A.

Moe GM, Legault L, Skorechi KL. Control of Extracelular Fluid Volume and Pathophysiology of Edema Formation. The Kidney. 1991:623-676.

Berkowitz HD, Shetty S. Renin release and renal cortical ischemia following aortic cross-clamping. Arch Surg. 1974;109:612-616.

Grindlinger GA, Vegas AM, William GH. Independence of renin production and hypertension in abdominal aortic aneurysmectomy. Am J Surg. 1981;141:472-477.

Hong SAH, Gelman S, Henderson T. Angiotensin and adrenoceptors in the hemodynamic response to aortic crossclamping. Arch Surg. 1992;127:438-441.

Gelman S, Curtis SE, Bradley WE. Angiotensin and adrenoreceptors role in hemodynamic response to aortic cross-clamping. Am J Physiol. 1993;264:H14-H20.

Ma D, Wang C, Pac-Soo CK. The effect of sevoflurane on spontaneous sympathetic activity, Adelta and C somatosympathetic reflexes, and associated hemodynamic changes in dogs. Anesth Analg. 1998;86:1079-1083.

Pac-Soo CK, Ma D, Wang C. Specific actions of halothane, isoflurane, and desflurane on sympathetic activity and Adelta and C somatosympathetic reflexes recorded in renal nerves in dogs. Anesthesiology. 1999;91:470-478.

Massone F. Anestesiologia Veterinária. 1999:225.

5ddc3ea80e8825d91af2c91e rba Articles
Links & Downloads

Braz J Anesthesiol

Share this page
Page Sections