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单次口服曲马多对胃分泌物pH值的影响。

Effect of single oral dose of tramadol on gastric secretions pH.

作者信息

Ullah Khan Mueen, Aqil Mansoor, Hussain Altaf, Al Zahrani Tariq, Hillis Marwan

机构信息

Department of Anesthesia, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

出版信息

Saudi J Anaesth. 2015 Jan;9(1):9-11. doi: 10.4103/1658-354X.146252.

DOI:10.4103/1658-354X.146252
PMID:25558191
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4279358/
Abstract

BACKGROUND

Tramadol is an atypical analgesic agent. It has been shown that intramuscular or intravenous injection tramadol is able to inhibit M3 muscarinic receptors. Tramadol is able to mediate smooth muscles contraction and glandular secretions. We have evaluated the effects of single oral dose of tramadol given preoperatively on gastric juices pH in patients electively scheduled for laparoscopic cholecystectomy.

MATERIALS AND METHODS

Sixty adult, American Society of Anesthesiologist I and II patients scheduled for laparoscopic cholecystectomy were included in the study. Patients were randomly assigned to receive either placebo (n = 30) or oral tramadol 50 mg (n = 30). General anesthesia was induced using propofol, fentanyl and cisatracurium. After induction of anesthesia 5 ml of gastric fluid was aspirated through orogastric tube. The gastric fluid pH was measured using pH meter.

RESULT

There was no significant difference in the pH between the groups. Gastric pH of the placebo and tramadol groups was 1.97 versus 1.98 (P = 0.092) respectively.

CONCLUSION

Preoperatively single oral dose of tramadol was unable to elevate the desired level of gastric acid secretions pH (>2.5). This may be due to pharmacokinetic disparity between the analgesic and pH elevating properties of tramadol.

摘要

背景

曲马多是一种非典型镇痛药。已表明肌内或静脉注射曲马多能够抑制M3毒蕈碱受体。曲马多能够介导平滑肌收缩和腺体分泌。我们评估了术前单次口服曲马多对择期行腹腔镜胆囊切除术患者胃液pH值的影响。

材料与方法

本研究纳入了60例计划行腹腔镜胆囊切除术的成年美国麻醉医师协会I级和II级患者。患者被随机分配接受安慰剂(n = 30)或口服曲马多50 mg(n = 30)。使用丙泊酚、芬太尼和顺式阿曲库铵诱导全身麻醉。麻醉诱导后,通过口胃管抽取5 ml胃液。使用pH计测量胃液pH值。

结果

两组之间的pH值无显著差异。安慰剂组和曲马多组的胃pH值分别为1.97和1.98(P = 0.092)。

结论

术前单次口服曲马多无法将胃酸分泌pH值提高到所需水平(>2.5)。这可能是由于曲马多的镇痛特性和提高pH值特性之间的药代动力学差异所致。

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本文引用的文献

1
Effects of varying doses of tramadol on gastric pH.不同剂量曲马多对胃内pH值的影响。
Anesth Essays Res. 2013 Jan-Apr;7(1):25-8. doi: 10.4103/0259-1162.113982.
2
Similar effects of tramadol and venlafaxine in major depressive disorder.曲马多和文拉法辛在重度抑郁症中的相似作用。
South Med J. 2008 Feb;101(2):193-5. doi: 10.1097/SMJ.0b013e3181616e66.
3
Pharmacological aspects of the effects of tramadol on G-protein coupled receptors.曲马多对G蛋白偶联受体作用的药理学方面
J Pharmacol Sci. 2007 Mar;103(3):253-60. doi: 10.1254/jphs.cr0060032.
4
Intramuscular tramadol increases gastric pH during anesthesia.
Can J Anaesth. 2004 Jun-Jul;51(6):545-8. doi: 10.1007/BF03018395.
5
The inhibitory effects of tramadol on muscarinic receptor-induced responses in Xenopus oocytes expressing cloned M(3) receptors.曲马多对表达克隆的M(3)受体的非洲爪蟾卵母细胞中由毒蕈碱受体诱导的反应的抑制作用。
Anesth Analg. 2002 Nov;95(5):1269-73, table of contents. doi: 10.1097/00000539-200211000-00031.
6
Tramadol inhibits norepinephrine transporter function at desipramine-binding sites in cultured bovine adrenal medullary cells.曲马多在培养的牛肾上腺髓质细胞中,于去甲丙咪嗪结合位点抑制去甲肾上腺素转运体功能。
Anesth Analg. 2002 Apr;94(4):901-6, table of contents. doi: 10.1097/00000539-200204000-00024.
7
Inhibition by tramadol of muscarinic receptor-induced responses in cultured adrenal medullary cells and in Xenopus laevis oocytes expressing cloned M1 receptors.曲马多对培养的肾上腺髓质细胞以及表达克隆M1受体的非洲爪蟾卵母细胞中由毒蕈碱受体诱导的反应的抑制作用。
J Pharmacol Exp Ther. 2001 Oct;299(1):255-60.
8
Pharmacokinetics of tramadol and bioavailability of enteral tramadol formulations. 4th communication: drops (without ethanol).曲马多的药代动力学及肠内曲马多制剂的生物利用度。第四次通讯:滴剂(不含乙醇)。
Arzneimittelforschung. 2000 Feb;50(2):99-108. doi: 10.1055/s-0031-1300173.
9
Bioavailability of tramadol after i.m. injection in comparison to i.v. infusion.与静脉输注相比,曲马多肌内注射后的生物利用度。
Int J Clin Pharmacol Ther. 1999 Apr;37(4):175-83.
10
Bioavailability of enteral tramadol formulations. 1st communication: capsules.肠内曲马多制剂的生物利用度。首次通讯:胶囊剂
Arzneimittelforschung. 1986 Aug;36(8):1278-83.