Sevoflurane does not alter norepinephrine-induced intracellular Ca2+ changes in the diabetic rat aorta
详细信息    查看全文
  • 作者:Keisuke Fujii MD (1)
    Koji Ogawa MD (2)
    Yasuyuki Tokinaga MD (2)
    Hiroshi Iranami MD (1)
    Yoshio Hatano MD (2)
  • 刊名:Canadian Journal of Anesthesia/Journal canadien d'anesth篓娄sie
  • 出版年:2010
  • 出版时间:December 2010
  • 年:2010
  • 卷:57
  • 期:12
  • 页码:1095-1101
  • 全文大小:379KB
  • 参考文献:1. / Jermendy G. Clinical consequences of cardiovascular autonomic neuropathy in diabetic patients. Acta Diabetol 2003; 40(Suppl 2): S370-4. CrossRef
    2. / Giorda CB, / Avogaro A, / Maggini M, / et al. Incidence and risk factors for stroke in type 2 diabetic patients: the DAI study. Stroke. 2007; 38: 1154-60. CrossRef
    3. / Koya D, / King GL. Protein kinase C activation and the development of diabetic complications. Diabetes 1998; 47: 859-66. CrossRef
    4. / Pierce GN, / Maddaford TG, / Russell JC. Cardiovascular dysfunction in insulin-dependent and non-insulin-dependent animal models of diabetes mellitus. Can J Physiol Pharmacol 1997; 75: 343-50. CrossRef
    5. / Negoro T, / Mizumoto K, / Ogawa K, / Hironaka Y, / Kakutani T, / Hatano Y. Effects of isoflurane and sevoflurane anesthesia on arteriovenous shunt flow in the lower limb of diabetic patients without autonomic neuropathy. Anesthesiology 2007; 107: 45-52. CrossRef
    6. / Yu J, / Ogawa K, / Tokinaga Y, / Iwahashi S, / Hatano Y. The vascular relaxing effects of sevoflurane and isoflurane are more important in hypertensive than normotensive rats. Can J Anesth 2004; 51: 979-85. CrossRef
    7. / Yu J, / Tokinaga Y, / Ogawa K, / Iwahashi S, / Hatano Y. Sevoflurane inhibits angiotensin II-induced, protein kinase C-mediated but not Ca2+-elicited contraction of rat aortic smooth muscle. Anesthesiology 2004; 100: 879-84. CrossRef
    8. / Yu J, / Ogawa K, / Tokinaga Y, / Hatano Y. Sevoflurane inhibits guanosine 5-[gamma-thio] triphosphate-stimulated, Rho/Rho-kinase-mediated contraction of isolated rat aortic smooth muscle. Anesthesiology 2003; 99: 646-51. CrossRef
    9. / Yu J, / Mizumoto K, / Tokinaga Y, / Ogawa K, / Hatano Y. The inhibitory effects of sevoflurane on angiotensin II-induced, p44/42 mitogen-activated protein kinase-mediated contraction of rat aortic smooth muscle. Anesth Analg 2005; 101: 315-21. CrossRef
    10. / Ramsey PH, / Ramsey PP. Power and type I errors for pairwise comparisons of means in the unequal variances case. Br J Math Stat Psychol 2009; 62(Pt 2): 263-81. CrossRef
    11. / Duncan ER, / Walker SJ, / Ezzat VA, / et al. Accelerated endothelial dysfunction in mild prediabetic insulin resistance: the early role of reactive oxygen species. Am J Physiol Endocrinol Metab 2007; 293: E1311-9. CrossRef
    12. / Cameron NE, / Cotter MA. Impaired contraction and relaxation in aorta from streptozotocin-diabetic rats: role of polyol pathway. Diabetologia 1992; 35: 1011-9. CrossRef
    13. / Taylor PD, / Oon BB, / Thomas CR, / Poston L. Prevention by insulin treatment of endothelial dysfunction but not enhanced noradrenaline-induced contractility in mesenteric resistance arteries from streptozotocin-induced diabetic rats. Br J Pharmacol 1994; 111: 35-41.
    14. / Fulton DJ, / Hodgson WC, / Sikorski BW, / King RG. Attenuated responses to endothelin-1, KCl and CaCl2, but not noradrenaline, of aortae from rats with streptozotocin-induced diabetes mellitus. Br J Pharmacol 1991; 104: 928-32.
    15. / Lenzen S. The mechanisms of alloxan- and streptozotocin-induced diabetes. Diabetologia 2008; 51: 216-26. CrossRef
    16. / Kawano K, / Hirashima T, / Mori S, / Natori T. OLETF (Otsuka Long-Evans Tokushima Fatty) rat: a new NIDDM rat strain. Diabetes Res Clin Pract 1994; 24: S317-20. CrossRef
    17. / Russell JC. Reduction and prevention of the cardiovascular sequelae of the insulin resistance syndrome. Curr Drug Targets Cardiovasc Haematol Disord 2001; 1: 107-20. CrossRef
    18. / Nobe K, / Sakai Y, / Maruyama Y, / Momose K. Hyper-reactivity of diacylglycerol kinase is involved in the dysfunction of aortic smooth muscle contractility in streptozotocin-induced diabetic rats. Br J Pharmacol 2002; 136: 441-51. CrossRef
    19. / Brondum E, / Kold-Petersen H, / Nilsson H, / Flyvbjerg A, / Aalkjaer C. Increased contractility to noradrenaline and normal endothelial function in mesenteric small arteries from the Goto-Kakizaki rat model of type 2 diabetes. J Physiol Sci 2008; 58: 333-9. CrossRef
    20. / Winters B, / Mo Z, / Brooks-Asplund E, / et al. Reduction of obesity, as induced by leptin, reverses endothelial dysfunction in obese (Lep(ob)) mice. J Appl Physiol 2000; 89: 2382-90.
    21. / Lesniewski LA, / Donato AJ, / Behnke BJ, / et al. Decreased NO signaling leads to enhanced vasoconstrictor responsiveness in skeletal muscle arterioles of the ZDF rat prior to overt diabetes and hypertension. Am J Physiol Heart Circ Physiol 2008; 294: H1840-50. CrossRef
    22. / Kobayashi T, / Matsumoto T, / Ooishi K, / Kamata K. Differential expression of alpha2D-adrenoceptor and eNOS in aortas from early and later stages of diabetes in Goto-Kakizaki rats. Am J Physiol Heart Circ Physiol 2004; 287: H135-43. CrossRef
    23. / Akata T, / Kanna T, / Yoshino J, / Takahashi S. Mechanisms of direct inhibitory action of isoflurane on vascular smooth muscle of mesenteric resistance arteries. Anesthesiology 2003; 99: 666-77. CrossRef
    24. / Akata T, / Nakashima M, / Izumi K. Comparison of volatile anesthetic actions on intracellular calcium stores of vascular smooth muscle: investigation in isolated systemic resistance arteries. Anesthesiology 2001; 94: 840-50. CrossRef
    25. / Yoo HJ, / Kozaki K, / Akishita M, / et al. Augmented Ca2?+?influx is involved in the mechanism of enhanced proliferation of cultured vascular smooth muscle cells from spontaneously diabetic Goto-Kakizaki rats. Atherosclerosis 1997; 131: 167-75. CrossRef
    26. / Evans JF, / Lee JH, / Ragolia L. Ang-II-induced Ca(2?+) influx is mediated by the 1/4/5 subgroup of the transient receptor potential proteins in cultured aortic smooth muscle cells from diabetic Goto-Kakizaki rats. Mol Cell Endocrinol 2009; 302: 49-57. CrossRef
    27. / Akata T. Cellular and molecular mechanisms regulating vascular tone. Part 2: regulatory mechanisms modulating Ca2?+?mobilization and/or myofilament Ca2?+?sensitivity in vascular smooth muscle cells. J Anesth 2007; 21: 232-42. CrossRef
    28. / Qi F, / Ogawa K, / Tokinaga Y, / Uematsu N, / Minonishi T, / Hatano Y. Volatile anesthetics inhibit angiotensin II-induced vascular contraction by modulating myosin light chain phosphatase inhibiting protein, CPI-17 and regulatory subunit, MYPT1 phosphorylation. Anesth Analg 2009; 109: 412-7. CrossRef
    29. / Mueed I, / Zhang L, / MacLeod KM. Role of the PKC/CPI-17 pathway in enhanced contractile responses of mesenteric arteries from diabetic rats to alpha-adrenoceptor stimulation. Br J Pharmacol 2005; 146: 972-82. CrossRef
  • 作者单位:Keisuke Fujii MD (1)
    Koji Ogawa MD (2)
    Yasuyuki Tokinaga MD (2)
    Hiroshi Iranami MD (1)
    Yoshio Hatano MD (2)

    1. Departments of Anesthesiology, Japanese Red Cross Society Wakayama Medical Centre, Wakayama, Japan
    2. Wakayama Medical University, Wakayama, Japan
文摘
Purpose The effect of volatile anesthetics on the mechanism(s) of vascular contraction in diabetes mellitus (DM) has not been fully understood. The current study was designed to determine the effects of sevoflurane on the norepinephrine (NE)-induced changes in contractile state and intracellular Ca2+ concentrations ([Ca2+]i) in the spontaneously developing type 2 DM rat. Methods The effects of sevoflurane on NE (10?M)-induced vasoconstriction and increase in [Ca2+]i in the aortas from Otsuka Long-Evans Tokushima Fatty (OLETF) rats, a type 2 DM model, and from age-matched control Long-Evans Tokushima Otsuka (LETO) rats were investigated using an isometric force transducer and fluorometer with fura-2 as an indicator of [Ca2+]i. Results Norepinephrine-induced increases in tension and [Ca2+]i in?OLETF?rats?were 54.8%, 95% confidence interval (CI) 36.9-72.6% and 58.8%, 95% CI 51.5-66.1%, respectively, and in LETO rats they were 46.4%, 95% CI 39.0-53.7% and 53.8%, 95% CI 46.9-60.7%, respectively,?when?expressed as the percentage relative to that induced by KCl 30?mM. In LETO rats, sevoflurane at a concentration of 3.4% inhibited the vascular contraction (9.4%, 95% CI 6.3-12.6%; P?<?0.001) and the increase in [Ca2+]i (33.3%, 95% CI 27.4-39.2%; P?=?0.002). In OLETF rats, however, sevoflurane failed to affect either the NE-induced contraction (43.6%, 95% CI 28.3-58.9%; P?=?0.68) or the elevation in [Ca2+]i (60.5%, 95% CI 56.3-64.8%; P?=?0.93). Conclusion Sevoflurane at clinically relevant concentrations inhibited the NE-induced increase in [Ca2+]i in the aortic smooth muscle from normal rats but not in that from type 2 DM rats. Thus, a Ca2+- signalling pathway resistant to sevoflurane appears to exist in the type 2 DM rat aorta.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700