Gebe tavşanlarda bupivakainin oluşturduğu epileptiform EEG aktivitesi üzerine efedrinin etkisi

Bu çalışmanın amacı gebe tavşanlara toksik dozlarda uygulanan bupivakaine eklenen efedrinin konvülziyon eşiği üzerine etkisini araştırmaktır. Yöntem: Araştırmaya 21 adet gebe tavşan alındı. Araştırmanın birinci günü, deneklerin her iki hemisferine EEG monitörizasyonu için soket yerleştirildi. İkinci gün uyanık ve spontan soluyan denekler randomize 3 gruba ayrıldı ve Grup Ve (n-7) 1.5 mg kg'dk' bupivakain; Grup 2'ye (n=7) 1.5 mg kg'dk1 bupivakain ile 50 fig kg'dk'1 efedrin; Grup 3'e (n=7) 1.5 mg kg'dk'1 bupivakain ile 100 ng kg1 dk1 efedrin intravenöz infüzyonlar şeklinde uygulandı. Bupivakain verilmesinden EEG'ye ait ilk diken-dalga kompleksinin oluşmasına kadar geçen süre ve verilen toplam ilaç dozları hesaplandı. Bazal, EEG'deki diken kompleksi oluşma sırasında ve 5 dakika sonrasındaki glukoz, Na+ ve K+ değerleri ölçüldü. Bulgular: Diken kompleksi gelişinceye kadar geçen ortalama süre Grup Vde 31.30 sn, Grup 2'de 24.53 sn ve Grup 3'de 10.37 sn olup tüm gruplarda anlamlı farklı bulundu (p

The effect of ephedrine sulfate on intravenous bupivacaine-induced epileptiform electroencephalogram activity in pregnant rabbits

Objective: To examine the role of ephedrine on the effects of convulsion thresholds caused by toxic doses ofbupivacaine. Methods: 21 pregnant rabbits were included in this study. On the first day of the study, sockets were placed on both hemispheres of all rabbits for monitoring the EEG signals. On the second day, the awake spontaneously breathing animals were divided into three groups randomly. Group 1 (n=7) was given 1.5 mg kg'min1 of bupivacaine; Group 2 (n=7) was given 1.5 mg kg'1 min'1 of bupivacaine with 50 ng kg^min'1 of ephedrine sulfate; and Group 3 (n=7) was given 1.5 mg kg min'1 of bupivacaine with 100 jig kg'1 min'1 of ephedrine sulfate as intravenous infusions. The time to appearance of spikes, the total drug doses with serum glucose, Na+ and K+ levels were measured at baseline, at the time of first EEG spike appearance and at 5 minutes later. Results: The spike times were measured as 31.30, 24.53 and 10.37 sec in Group 1, 2 and 3 respectively and the differences among them were statistically significant (p<0.01). Total bupivacaine doses were 2.28,1.6 and 0.7 mg in the groups respectively and the difference between the groups were significant (p<0.01). There were no differences in total ephedrine doses between the groups. Conclusion: The result of our study showed that ephedrine decreases the threshold of convulsion in pregnant rabbits receiving toxic doses of bupivacaine.

___

  • 1. Santos AC, Arthur GR, Wlody D, De Armas P, Morishima HO, Finster M. Comparative systemic toxicity of ropivacaine and bu pivacaine in nonpregnant and pregnant ewes. Anesthesiology 1995; 82: 734-40.
  • 2. Dony P, Dewinde V, Vanderick B ve ark. The comparative toxicity of ropivacaine and bupivacaine at equipotent doses in rats. Anesth Analg 2000;91: 1489-92.
  • 3. Murao K, Shingu K, Tsushima K, Takahira K, Ikeda S, Nakao S. The anticonvulsant effects of volatile anesthetics on lidocaine-in duced seizures in cats. Anesth Analg 2000; 90: 142-7.
  • 4. Rutten AJ, Nancarrow C, Mather LE, Ilsley AH, Runciman WB, Upton RN. Hemodynamic and central nervous system effects of intravenous bolus doses of lidocaine, bupivacaine, and ropivaca ine in sheep. Anesth Analg 1989; 69: 291-9.
  • 5. Robinson J, Fernando R, Sun Wai WY, Reynolds F. Chemical sta bility of bupivacaine, lidocaine and epinephrine in pH-adjusted solutions. Anaesthesia 2000; 55: 853-8.
  • 6. Momota Y, Artru AA, Powers KM, Mautz DS, Ueda Y. Posttreat ment with propofol terminates lidocaine-induced epileptiform electroencephalogram activity in rabbits: effects on cerebrospinal fluid dynamics. Anesth Analg 1998; 87: 900-6.
  • 7. Yokoyama M, Hirakawa M, Goto H. Effect of vasoconstrictive a gents added to lidocaine on intravenous lidocaine-induced convul sions in rats. Anesthesiology 1995; 82: 574-80.
  • 8. Burns SM, Cowan CM, Wilkes RG. Prevention and management of hypotension during spinal anaesthesia for elective Caesarean section: a survey of practice. Anaesthesia 2001; 56: 794-8.
  • 9. Fong J, Gurewitsch ED, Press RA, Gomillion MC, Volpe L. Pre vention of maternal hypotension by epidural administration of ep hedrine sulfate during lumbar epidural anesthesia for cesarean section. Am J Obstet Gynecol 1996; 175: 985-90.
  • 10. Ngan Kee WD, Khaw KS, Lee BB, Lau TK, Gin T. A dose-response study of prophylactic intravenous ephedrine for the preven tion of hypotension during spinal anesthesia for cesarean delivery Anesth Analg 2000; 90: 1390-5.
  • 11. Bernards CM, Artru AA. Effect of intracerebrovehtricular picroto xin and muscimol on intravenous bupivacaine toxicity. Evidence supporting central nervous system involvement in bupivacaine cardiovascular toxicity. Anesthesiology 1993; 78: 902-10.
  • 12. Bernards CM, Carpenter RL, Renter ME, Brown DL, Rupp SM, Thompson GE. Effect of epinephrine on central nervous system and cardiovascular system toxicity of bupivacaine in pigs. Anest hesiology 1989; 71: 711-7.
  • 13. Huang YF, Pryor ME, Mather LE, Veering BT.Cardiovascular and central nervous system effects of intravenous levobupivacaine and bupivacaine in sheep.Anesth Analg 1998; 86: 797-804.
  • 14. Nancarrow C, Rutten AJ, Runciman WB ve ark. Myocardial and cerebral drug concentrations and the mechanisms of death after fatal intravenous doses of lidocaine, bupivacaine, and ropivacaine in the sheep.Anesth Analg 1989; 69: 276-83.
  • 15. Avery P, Redon D, Schaenzer G, Rusy B. The influence of serum potassium on the cerebral and cardiac toxicity of bupivacaine and lidocaine. Anesthesiology 1984; 61: 134-8.
  • 16. Skeie B, Meidell NK, Steen PA. Long-term bupivacaine infusion does not alter the acute seizure threshold to bupivacaine in rats. Anesth Analg 1988; 67: 61-3.
  • 17. Spiegel DA, Dexter F, Warner DS, Baker MT, Todd MM. Central nervous system toxicity of local anesthetic mixtures in the rat. Anesth Analğ 1992; 75: 922-8.
  • 18. Santos AC, Pedersen H, Harmon TW ve ark. Does pregnancy al ter the systemic toxicity of local anesthetics? Anesthesiology 1989; 70: 991-5.
  • 19. Bucklin BA, Warner DS, Choi WW, Todd MM, Chestnut DH. Pregnancy does not alter the threshold for lidocaine-induced se izures in the rat. Anesth Analg 1992; 74: 57-61.
  • 20. Morishima HO, Pedersen H, Finster M ve ark. Bupivacaine toxicity in pregnant and nonpregnant ewes. Anesthesiology 1985; 63: 134-9.
  • 21. Momota Y, Artru AA, Powers KM, Mautz DS, Ueda Y. Concent rations of lidocaine and monoethylglycine xylidide in brain, cerebrospinal fluid, and plasma during lidocaine-induced epilepti form electroencephalogram activity in rabbits: the effects of epinephrine and hypocapnia. Anesth Analg 2000; 91: 362-8.
  • 22. Torbiner ML, Yagiela JA, Mito RS. Effect of midazolam pretreatment on the intravenous toxicity of lidocaine with and without epinephrine in rats. Anesth Analg 1989; 68: 744-9.
  • 23. Johansson BB, Martinsson L. Blood-brain barrier to albumin in awake rats in acute hypertension induced by adrenaline, noradre naline or angiotensin. Acta Neurol Scand 1979; 60: 193-7.
  • 24. Takahashi R, Oda Y, Tanaka K, Morishima HO, Inoue K, Asada A. Epinephrine increases the extracellular lidocaine concentration in the brain: a possible mechanism for increased central nervous system toxicity. Anesthesiology 2006; 105: 984-9.