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呋喃妥因在犬肝胆汁中的排泄。

Excretion of nitrofurantoin in dog hepatic bile.

作者信息

Conklin J D, Wagner D L

出版信息

Br J Pharmacol. 1971 Sep;43(1):140-50. doi: 10.1111/j.1476-5381.1971.tb07163.x.

Abstract
  1. After the intravenous administration of nitrofurantoin sodium to dogs at nitrofurantoin doses of 1.5-24.0 mg/kg, a substantial amount of nitrofurantoin is excreted in bile. The bile to blood drug ratios were about 200. A marked hydrocholeretic effect which correlated directly with the amount of nitrofurantoin administered was also observed.2. The excretion of nitrofurantoin in bile and the hydrocholeretic effect were linear with the dose of drug over the range 1.5-12.0 mg/kg. Maximum increases in hepatic bile flows were usually from 5-10 ml/0.5 h, while average control bile flow was 1.6 ml +/- S.D. 0.6/0.5 hours. The lowest dose at which the hydrocholeretic effect was still detectable was 0.09 mg/kg.3. Apparent saturation of the biliary excretion system for nitrofurantoin and the hydrocholeretic mechanism occurred after a dose of 24.0 mg/kg. Saturation of the urinary system for nitrofurantoin excretion was noted after a dose of 6.0 mg/kg.4. Biliary nitrofurantoin recoveries ranged from 16.5% +/- S.D. 4.2 to 22.6% +/- S.D. 4.7 for the 6 h period after doses of 1.5, 3.0, and 6.0 mg/kg. Urinary nitrofurantoin recoveries for the same interval ranged from 24.1% +/- S.D. 6.6 to 36.2% +/- S.D. 8.3.5. In comparison to values obtained in normal dogs, only about one-tenth of the drug excretion in bile and about one-fifth of the hydrocholeretic effect were obtained after intravenous drug administration to dogs with hepatic impairment induced by CCl(4).
摘要
  1. 以1.5 - 24.0毫克/千克的呋喃妥因剂量给犬静脉注射呋喃妥因钠后,大量呋喃妥因经胆汁排泄。胆汁与血液的药物比率约为200。还观察到明显的利胆作用,且该作用与呋喃妥因给药量直接相关。

  2. 在1.5 - 12.0毫克/千克的剂量范围内,呋喃妥因在胆汁中的排泄及利胆作用与药物剂量呈线性关系。肝胆汁流量的最大增加通常为5 - 10毫升/0.5小时,而对照胆汁平均流量为1.6毫升±标准差0.6/0.5小时。仍可检测到利胆作用的最低剂量为0.09毫克/千克。

  3. 在24.0毫克/千克的剂量后,呋喃妥因的胆汁排泄系统和利胆机制出现明显饱和。在6.0毫克/千克的剂量后,注意到呋喃妥因排泄的泌尿系统出现饱和。

  4. 在1.5、3.0和6.0毫克/千克剂量后的6小时内,胆汁中呋喃妥因的回收率为16.5%±标准差4.2至22.6%±标准差4.7。同一时间段内尿液中呋喃妥因的回收率为24.1%±标准差6.6至36.2%±标准差8.3。

  5. 与正常犬获得的值相比,给四氯化碳诱导肝损伤的犬静脉给药后,胆汁中药物排泄量仅约为正常犬的十分之一,利胆作用约为正常犬的五分之一。

相似文献

1
Excretion of nitrofurantoin in dog hepatic bile.呋喃妥因在犬肝胆汁中的排泄。
Br J Pharmacol. 1971 Sep;43(1):140-50. doi: 10.1111/j.1476-5381.1971.tb07163.x.
4
Biopharmaceutics of nitrofurantoin.
Pharmacology. 1972;8(1):178-81.
5
Effect of choleretics on biliary and urinary excretion of cholecystographic agents.
Invest Radiol. 1975 May-Jun;10(3):189-96. doi: 10.1097/00004424-197505000-00001.
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Urinary drug excretion in dogs during therapeutic doses of different nitrofurantoin dosage forms.
J Pharm Sci. 1969 Nov;58(11):1365-8. doi: 10.1002/jps.2600581114.

本文引用的文献

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Studies on the distribution and excretion of certain nitrofurans.
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Renal tubular transport of nitrofurantoin.
Am J Physiol. 1962 Jun;202:1136-40. doi: 10.1152/ajplegacy.1962.202.6.1136.
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Mechanisms of bile secretion.胆汁分泌的机制。
J Am Med Assoc. 1959 Mar 28;169(13):1462-6. doi: 10.1001/jama.1959.03000300058011.
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Treatment of urinary infections; choice of drug.
Tex State J Med. 1953 Oct;49(10):761-5.
9
Mechanisms of bile formation.胆汁形成的机制。
Am J Physiol. 1952 Oct;171(1):62-74. doi: 10.1152/ajplegacy.1952.171.1.62.

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