Vasospasmus cévní stopky laloku – magnesium sulfuricum snižuje vasospasmus cévní stopky axiálního laloku na prasečím modelu
Autoři:
P. Hyza 1; L. Streit 1; Gopfert E. D. V. M. 2; Z. Dvorak 1; I. Stupka 1; D. Schwarz 3; T. Kubek 1; Lombardo G. A. G. 1; J. Veselý 1
Působiště autorů:
Department of Plastic and Aesthetic Surgery, St. Anne University Hospital, Brno, Czech Republic
1; Veterinary Research Institute, Brno, Czech Republic
2; Institute of Biostatistics and Analyse, Masaryk University, Brno, Czech Republic
3
Vyšlo v časopise:
ACTA CHIRURGIAE PLASTICAE, 57, 1-2, 2015, pp. 4-8
Zdroje
1. Acland RD. Factors that influence success in microvascular surgery. In: Serafin D, Buncke HJ. eds. Microsurgical Composite Tissue Transplantation. St. Louis, Mo: CV Mosby Co; 1979:76–82.
2. Puckett CL, Winters RW, Geter RK, Goebel D: Studies of pathologic vasoconstriction (vasospasm) in microvascular surgery. J Hand Surg. 1985;10:343–9.
3. Vesely J, Samohyl J, Barinka L, Nemec A. Tissue shock in free flaps in the experiment on the rat. Significance, classification and effect. Handchir Mikrochir Plast Chir. 1987;19:269–72.
4. Vesely J, Samohyl, J, Barinka L, Nemec A, Smrcka V. Spastic complications in free flap transfers. Rozhl Chir. 1990;69:682–88.
5. Weinzweig N, Gonzalez M. Free tissue failure is not an all-or-none phenomenon. Plast Reconstr Surg. 1995;96:648–60.
6. Jurell G, Hjemdahl P, Fredholm BB. On the mechanism by which antiadrenergic drugs increase survival of critical skin flaps. Plast Reconstr Surg. 1983;72:518–25.
7. Goshen J, Wexler MR, Peled IJ. The use of two alpha blocking agents, phenoxybenzamine and phentolamine, in ointment and injection form to improve skin flap survival in rats. Ann Plast Surg. 1985;15:431–5.
8. Evans GR, Gherardini G, Gurlek A, Langstein H, Joly GA, Cromeens DM, et. al. Drug-induced vasodilation in an in vitro and in vivo study: the effects of nicardipine, papaverine and lidocaine on the rabbit carotid artery. Plast Reconstr Surg. 1997;100:1475–81.
9. Gürlek A, Gherardini G, Cromeens D, Joly GA, Wang B, Evans GR. Drug-induced vasodilation: the effects of sodium nitroprusside, hydralazine, and cromakalin on the rabbit carotid artery: in vitro and in vivo study. J Reconstr Microsurg. 1997;13:415–21.
10. Angel MF, Schieren G, Jorysz M, Knight KR, O’Brien BM. The beneficial effect of chlorpromazine on dorsal skin flap survival. Ann Plast Surg. 1989;23:492–7.
11. Emery FM, Kodey TR, Bomberger RA, McGregor DB. The effect of nifedipine on skin-flap survival. Plast Reconstr Surg. 1990;85:61–3.
12. Gherardini G, Jernbeck J, Samuelson U, Hedén P. Effects of calcitonin gene-related peptide and lidocaine on mechanically induced vasospasm in an island flap in the rat. J Reconstr Microsurg. 1995;11:179–83.
13. Gherardini G, Samuelson U, Jernbeck J, Aberg B, Sjöstrand N. Comparison of vascular effects of ropivicaine and lidocaine on isolated rings of human arteries. Acta Anaesth Scand. 1995;39:765–8.
14. Gherardini G, Evans GR, Theodorsson E, Gurlek A, Milner SM, Palmer B, et al. Calcitonin gene-related peptide in experimental ischemia: Implications of an endogenous anti-ischemic effect. Ann Plast Surg. 1996;36:616–20.
15. Jernbeck J, Samuelson UE. Effects of lidocaine and calcitonin gene-related peptide (CGRP) on isolated human radial arteries. J Reconstr Microsurg. 1993;9:361–5.
16. Johns RA, DiFazio CA, Longnecker DE. Lidocaine constricts or dilates rat arterioles in a dose-dependent manner. Anesthesiology. 1985;62:141–4.
17. Pang CY, Chiu C, Zhong A, Xu N. Pharmacologic intervention of skin vasospasm and ischemic necrosis in pigs. J Cardiovasc Phamacol. 1993;21:163–71.
18. Massey MF, Gupta DK. The effects of systemic phenylephrine and epinephrine on pedicle artery and microvascular perfusion in a pig model of myoadipocutaneous rotational flaps. Plast Reconstr Surg. 2007;120:1289–99.
19. Nunes S, Berg L, Raittinen LP, Ahonen H, Laranne J, Lindgren L. Deep sedation with dexmedetomidine in a porcine model does not compromise the viability of free microvascular flap as depicted by microdialysis and tissue oxygen tension. Anesth Analg. 2007;105:666–72.
20. Pang CY, Zhang J, Xu H, Lipa JE, Forrest CR, Neligan PC. Role and mechanism of endothelin-B receptors in mediating ET-1-induced vasoconstriction in pig skin. Am J Physiol. 1998;275:R1066–74.
21. Pang CY, Yang RZ, Neligan P, Xu N, Chiu C, Zhong A, et al. Vascular effects and mechanism of action of endothelin-1 in isolated perfused pig skin. J Appl Physiol. 1995;79:2106–13.
22. Pang CY, Neligan PC, Forrest CR, Nakatsuka T, Sasaki GH. Hemodynamics and vascular sensitivity to circulating norepinephrine in normal skin and delayed and acute random skin flaps in the pig. Plast Reconstr Surg. 1986;78:75–84.
23. Hyza P, Streit L, Gopfert E, Schwarz D, Masarik M, Jurajda M. et. al. Gene expression of the Endothelin-1 in vasospastic flap pedicle – an experimental study on a porcine model. Acta Vet Brno. 2010;79:453–7.
24. Cummings CW, Trachy RE, Richardson MA, Patterson HC. Prognostication of myocutaneous flap viability using laser Doppler velocimetry and fluorescein microfluorometry. Otolaryngol Head Neck Surg. 1984;92:559–63.
25. Marks NJ. Quantitative analysis of skin flap blood flow in the rat using laser Doppler velocimetry. J R Soc Med. 1985;78:308–14.
26. Wingard CJ, Browne AK, Murphy RA. Dependence of force on length at constant cross-bridge phosphorylation in the swine carotid media. J Physiol. 1995,488:729–39.
27. Altura BT, Altura BM. Withdrawal of magnesium causes vasospasm while elevated magnesium produces relaxation of tone in cerebral arteries. Neurosci Lett. 1980;20:323–27.
28. Altura BM, Altura BT. Magnesium ions and contraction of vascular smooth muscle. Fed Proc. 1981;40:2672–9.
29. Kimura T, Yasue H, Sakaino N, Rokutanda M, Jouga–Saki M, Araki H. Effects of magnesium on the tone of isolated human coronary arteries. Circulation. 1989;79:1118–24.
30. Noguera MA, Dócon MP. Modulatory role of magnesium on the contractile response of rat aorta to several agonists in normal and calcium-free medium. J Pharm Pharmacol. 1993;45:697–700.
31. Chi OZ, Pollack P, Weiss HR. Effects of magnesium sulphate and nifedipine on regional cerebral blood flow during middle cerebral artery ligation in the rat. Arch Int Pharmacodyn Ther. 1990;304:196–205.
32. Dipette DJ, Simpson K, Guntupalli J. Systemic and regional hemodynamic effect of acute magnesioum administration in the normotensive and hypertensive state. Magnesium. 1987;6:136–49.
33. Kemp PA, Gardiner SM, Bennett T, Rubin PC. Magnesium sulphate reverses carotid vasoconstriction caused by endothelin 1, angiotensin II and neuropeptide –Y, but not that caused by N-nitro-L-arginine methyl ester, in conscious rats. Clin Sci. 1993;85:175–81.
34. Kemp PA, Gardiner SM, March JE, Bennett T, Rubin PC. Effects of NG-nitro-L-arginine methyl ester on regional hemodynamic responses to MgSO4 in conscious rats. Br j Pharmacol. 1994;111:325–31.
35. Weber A, Herz R, Reiss I. The role of magnesium in the relaxation of myofibrils. Biochemistry. 1969;8:2266–71.
36. Sjögren A, Edvinsson L. The influence of magnesium on the release of calcium from intracellular depots in vascular smooth muscle cells. Pharmacol Toxicol. 1988;62:17–21.
37. Strauss JD, Murphy RA. Regulation of cross bridge cycling. In: Barany M eds. Biochemistry of Smooth Muscle Contraction. San Diego, CA: Academic Press; 1996:341–53.
38. Moreland RS, Ford GD. The influence of magnesium on calcium-activated, vascular smooth muscle actomyosin ATPase activity. Arch Biochem Biophys. 1981;208:325–33.
39. Johnson JW, Ascher P. Voltage-dependent block by intracellular Mg2+ of N-methyl-D-aspartate-activated channels. Biophys J. 1990;57:1085–90.
40. Altura BM, Altura BT, Carella A, Gebrewold A, Hurakawa T, Nishio A. Mg2+-Ca2+ interaction in contractility of vascular smooth muscle: Mg2+ versus organic calcium channel blockers on myogenic tone and agonist-induced responsiveness of blood vessels. Can J Physiol Pharmacol. 1987;65:729–45.
41. Ram Z, Sadeh M, Shacked I, Sahar A, Hadani M. Magnesium sulphate reverses experimental delayed cerebral vasospasm after subarachnoid hemorrhage in rats. Stroke. 1991;22:922–27.
42. Chia RY, Hughes RS, Morgan MK. Magnesium: a useful adjunct in the prevention of cerebral vasospasm following aneurysmal subarachnoid hemorrhage. J Clin Neurosci. 2002;9:279–81.
43. Boet R, Mee E. Magnesium sulfate in the management of patients with Fisher grade 3 subarachnoid hemorrhage: a pilot study. Neurosurgery. 2000;47:602–7.
44. van den Bergh WM, Algra A, van Kooten F, Dirven CM, van Gijn J, Vermeulen M. Magnesium sulfate in aneurysmal subarachnoid hemorrhage. A randomized controlled trial. Stroke. 2005;36:1011–15.
45. Wong GK, Chan MT, Boet R, Poon WS, Gin T. Intravenous magnesium sulfate after aneurysmal subarachnoid hemorrhage: a prospective randomized pilot study. J Neurosurg Anesthesiol. 2006;18:142–8.
46. Pyne GJ, Cadoux-Hudson TA, Clark JF. Magnesium protection against in vitro cerebral vasospasm after subarachnoid hemorrhage. Br J Neurosurg. 2001;15:409–15.
Štítky
Chirurgie plastická Ortopedie Popáleninová medicína TraumatologieČlánek vyšel v časopise
Acta chirurgiae plasticae
2015 Číslo 1-2
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