Calcium Channel Blockade in Rats with Cyclosporine-Induced Vasoconstriction

References

• Dawidson I, Rooth P, Fry W R, et al. Prevention of acute cyclosporine-induced renal blood flow inhibition and improved immunosuppression with verapamil. Transplantation 1989; 48: 575–580
   PubMed Web of Science ®Google Scholar
• Dawidson I, Rooth P, Alway C, et al. Verapamil prevents posttransplant delayed function and cyclosporine A nephrotoxicity. Transplant Proc 1990; 22: 1379–1380
   PubMed Web of Science ®Google Scholar
• Morales J M, Andres A, Alvarez C, et al. Calcium channel blockers and early cyclosporine nephrotoxicity after renal transplantation: a prospective randomized study. Transplant Proc 1990; 22: 1733–1735
   PubMed Web of Science ®Google Scholar
• Feehally J, Walls J, Mistry N, et al. Does nifedipine ameliorate cyclosporine A nephrotoxicity?. Br Med J. [Clin Res] 1987; 295: 310
   PubMedGoogle Scholar
• Rooth P, Dawidson, Diller K, Täljedal I B. Protection against cyclosporine-induced impairment of renal microcirculation by verapamil in mice. Transplantation 1988; 45: 433–437
   PubMed Web of Science ®Google Scholar
• Rooth P, Dawidson I, Clothier N, Diller K. In vivo florescence microscopy of kidney subcapsular blood flow in mice. Effects of cyclosporine (NVA2)-cyclosporine, and isradipine, a new calcium antagonist. Transplantation 1988; 46: 566–569
   PubMed Web of Science ®Google Scholar
• Iaina A, Herzog D, Cohen D, et al. Calcium entry-blockade with verapamil in cyclosporine A plus ischemia induced acute renal failure in rats. Clin Nephrol 1986; 25(Suppl 1)S168–S170
   Google Scholar
• Sumpio B, Baue A E, Chaudry I H. Treatment with verapamil and adenosine triphosphate-MgCl2 reduces cyclosporine nephrotoxicity. Surgery 1987; 101: 315–322
   PubMed Web of Science ®Google Scholar
• Steinhausen M, Snoei H, Parekh N, Baker R, Johnson P C. Hydronephrosis: A new method to visualize vas afferens, efferens and glomerular network. Kidney Int 1983; 23: 794–806
   PubMedGoogle Scholar
• Steinhausen M, Sterzel R B, Fleming J T, Kühn R, Weis S. Acute and chronic effects of angiotensin II on the vessels of the split hydronephrotic kidney. Kidney Int 1987; 20(Suppl)S64–S73
   Google Scholar
• Steinhausen M, Weis S, Fleming J T, Dussel R, Parekh N. Responses of in vivo renal microvessels to dopamine. Kidney Int 1986; 30: 361–370
   PubMed Web of Science ®Google Scholar
• Fleming J T, Parekh N, Steinhausen M. Calcium antagonists preferentially dilate preglomerular vessels of hydronephrotic kidney. Am J Physiol 1987; 253(6)F1157–F1163, (Pt 2)
   Google Scholar
• Abraham J S, Bentley F R, Garrison R N, Cryer H M. Cyclosporine A directly constricts intrarenal arterioles. Transplant Proc 1991; 23: 356–359
   PubMedGoogle Scholar
• Longnecker D E, Harris P D. Microcirculatory actions of general anaesthetics. Fed Proc 1980; 39: 1580–1583
   PubMedGoogle Scholar
• Faber J E, Harris P D, Wiegman D L. Anaesthetic depression of microcirculation, central hemodynamics, and respiration in decerebrate rats. Am J Physiol 1982; 243: H837–H843
   Google Scholar
• Faber J E, Harris P D, Miller F N. Microvascular sensitivity to PGE2 and PGI2 in skeletal muscle of decerebrate rat. Am J Physiol 1982; 243: H844–H851
   PubMed Web of Science ®Google Scholar
• Isomaya T, Sato T, Tanaka J, Shatney C H. Measurement of cardiac output in small animals by aortic thermodilution. J Surg Res 1982; 33: 170–176
   PubMedGoogle Scholar
• Lipowsky H H, Zweifach B W. Application of the “two-slit” photometric technique to the measurement of microvascular volumetric flow rates. Microvasc Res 1978; 15: 93–101
   PubMed Web of Science ®Google Scholar
• Murray B M, Paller M S, Ferris T F. Effect of cyclosporine administration on renal hemodynamics in conscious rats. Kidney Int 1985; 28: 767–774
   PubMed Web of Science ®Google Scholar
• Humes H D, Jackson N M, O'Connor R P, Hunt D A, White M D. Pathogenic mechanisms of nephrotoxicity: insights into cyclosporine nephrotoxicity. Transplant Proc 1985; 17: 51–61
   PubMed Web of Science ®Google Scholar
• Sullivan B A, Hak L J, Finn W F. Cyclosporine nephrotoxicity: studies in laboratory animals. Transplant Proc 1985; 17(Suppl 1)145–153
   PubMed Web of Science ®Google Scholar
• Sabbatini M, Esposito C, Ucuello F, et al. Acute effects of cyclosporine on glomerular dynamics-micropuncture study in the rat. Transplant Proc 1988; 20(Suppl 3)544–548
   PubMedGoogle Scholar
• Curtis J J, Luke R G, Dubovsky J D, Diethelm A G, Whelchel J D, Jones P. Cyclosporin in therapeutic doses increases renal allograft vascular resistance. Lancet 1985; 2: 477–479
   Google Scholar
• Buhrle C P, Hackenthal E, Helmchen U, et al. The hydronephrotic kidney of the mouse as a tool for intravital microscopy and in vitro electrophysiological studies of renin-containing cells. Lab Invest 1986; 54: 462–472
   PubMedGoogle Scholar
• Buhrle C P, Mobiling R, Mannek E, Schneider D, Hackenthal E, Taugner R. The afferent arteriole: immunocytochemical and electrophysiological investigations. J Cardiovasc Pharmacol 1984; 6: S383–S393
   Google Scholar
• Anaise D, Lane B, Waltzer W C, Rapaport F T. The protective effect of calcium inhibitors and of captopril on the renal microcirculation during reperfusion. Transplantation 1987; 43: 128–133
   PubMedGoogle Scholar
• Loutzenhiser R, Epstein M. Effects of calcium antagonists on renal hemodynamics. Am J Physiol 1985; 249: F619–F629
   PubMed Web of Science ®Google Scholar
• Loutzenhiser R, Epstein M, Horton C, Sonke P. Reversal of prostaglandin vasoconstriction by diltiazem: studies in isolated smooth muscle and perfused rat kidney (Abstr). Kidney Int 1985; 27: 296
   Google Scholar
• Moss N G, Powell S L, Falk R J. Intravenous cyclosporine activates afferent and efferent renal nerves and causes sodium retention in innervated kidneys in rats. Proc Natl Acad Sci USA 1985; 82: 8222–8226
   PubMed Web of Science ®Google Scholar
• Murray B M, Paller M S. Beneficial effects of renal denervation and prazosin on GFR and renal blood flow after cyclosporine in rats. Clin Nephrol 1986; 25(Suppl 1)S37–S39
   PubMedGoogle Scholar
• Xue H, Bukoski R D, McCarron D A, Bennett W M. Induction of contraction in isolated rat aorta by cyclosporine. Transplantation 1987; 43: 715–718
   PubMed Web of Science ®Google Scholar