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Renal targeting of a non-steroidal anti-inflammatory drug: effects on renal prostaglandin synthesis in the rat.

作者信息

Haas M, Moolenaar F, Meijer D K, de Jong P E, de Zeeuw D

机构信息

Department of Internal Medicine, Division of Nephrology, Groningen Institute for Drug Studies, University Hospital, Hanzeplein 1, NL-9713 GZ Groningen, The Netherlands.

出版信息

Clin Sci (Lond). 1998 Nov;95(5):603-9. doi: 10.1042/cs0950603.

DOI:10.1042/cs0950603
PMID:9791047
Abstract
  1. Renal specific targeting of the non-steroidal anti-inflammatory drug naproxen was obtained by coupling to the low-molecular-mass protein lysozyme. A previous study showed that conjugation to lysozyme resulted in a 70-fold increase of naproxen accumulation in the kidney with a subsequent renal release of the active metabolite naproxen-lysine.2. In the present study we questioned whether naproxen-lysozyme is active in the rat kidney, inhibiting the urinary excretion of prostaglandin E2 and renal sodium and water excretion in salt-restricted baseline conditions as well as during frusemide treatment.3.A high dose of free naproxen (10 mg.day-1. kg-1) did not affect prostaglandin E2 excretion in baseline conditions (naproxen, 11+/-1 ng/8 h; vehicle, 13+/-4 ng/8 h), whereas sodium and water excretion were, respectively, 3.0 and 1.6 times lower in the naproxen group (P<0.05). Naproxen completely prevented the frusemide-induced increase (3-fold) in prostaglandin E2 excretion (naproxen 6.6+/-1.1 ng/8 h, vehicle 40+/-12 ng/8 h, P<0. 005). Frusemide-stimulated natriuresis and diuresis were, respectively, 1.6 (P<0.05) and 1.8 times (P<0.005) lower in the naproxen group.4.A dose of 2 mg.day-1.kg-1 lysozyme-conjugated naproxen did not affect prostaglandin E2 excretion in baseline conditions (conjugate, 18+/-2 ng/8 h; vehicle, 24+/-5 ng/8 h). The conjugate also had no effect on sodium and water excretion. However, the naproxen conjugate completely prevented the frusemide-induced increase (2-fold) in prostaglandin E2 excretion (conjugate, 16+/-3 ng/8 h; vehicle, 48+/-13 ng/8 h, P<0.05). Surprisingly, frusemide-induced natriuresis and diuresis were not affected by the conjugate.5. In conclusion, a renal specific delivery of the non-steroidal anti-inflammatory drug naproxen using lysozyme results in an inhibitory effect on renal prostaglandin E2 synthesis but does not affect the excretion of sodium and water, in contrast to free naproxen.
摘要

相似文献

1
Renal targeting of a non-steroidal anti-inflammatory drug: effects on renal prostaglandin synthesis in the rat.
Clin Sci (Lond). 1998 Nov;95(5):603-9. doi: 10.1042/cs0950603.
2
Drug-targeting to the kidney: renal delivery and degradation of a naproxen-lysozyme conjugate in vivo.药物靶向肾脏:萘普生-溶菌酶缀合物在体内的肾脏递送与降解
Kidney Int. 1997 Dec;52(6):1693-9. doi: 10.1038/ki.1997.504.
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Attenuation by phenylbutazone of the renal effects and excretion of frusemide in horses.苯基布他松对马体内速尿的肾脏效应及排泄的抑制作用
Equine Vet J. 1999 Jul;31(4):289-95. doi: 10.1111/j.2042-3306.1999.tb03819.x.
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Effects of prostaglandin synthesis inhibitors on the renin-angiotensin system and renal function.前列腺素合成抑制剂对肾素-血管紧张素系统及肾功能的影响。
Hypertension. 1985 Sep-Oct;7(5):791-6. doi: 10.1161/01.hyp.7.5.791.
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Low molecular weight proteins as carriers for renal drug targeting: naproxen-lysozyme.
Pharm Res. 1991 Oct;8(10):1223-30. doi: 10.1023/a:1015835325321.
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The interaction of paracetamol with frusemide.对乙酰氨基酚与呋塞米的相互作用。
Br J Clin Pharmacol. 1994 May;37(5):464-7. doi: 10.1111/j.1365-2125.1994.tb05716.x.
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[Role of prostaglandin E2 in regulation of urine excretion in saluresis, water and osmotic diuresis in rat].[前列腺素E2在大鼠水利尿、水和渗透性利尿中对尿排泄调节的作用]
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