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

被引:11
|
作者
Haas, M
Moolenaar, F
Meijer, DKF
de Jong, PE
de Zeeuw, D
机构
[1] Univ Groningen Hosp, Groningen Inst Drug Studies, Dept Internal Med, Div Nephrol, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Groningen Inst Drug Studies, Dept Pharmacokinet & Drug Delivery, NL-9713 AV Groningen, Netherlands
[3] Univ Groningen, Groningen Inst Drug Studies, Dept Clin Pharmacol, NL-9713 AV Groningen, Netherlands
关键词
drug targeting; kidney; low-molecular-mass protein; lysozyme; naproxen; non-steroidal anti-inflammatory drug; prostaglandins;
D O I
10.1042/cs0950603
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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 E-2 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 E-2 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 E-2 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 E-2 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 E-2 excretion (conjugate, 16 +/- 3 ng/8 h; vehicle, 48 +/- 1 3 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 E-2 synthesis but does not affect the excretion of sodium and water, in contrast to free naproxen.
引用
收藏
页码:603 / 609
页数:7
相关论文
共 50 条
  • [1] Renal damage induced by non-steroidal anti-inflammatory drug treatment
    Para, Ioana
    Ciumarnean, Lorena
    Alexescu, Teodora
    Domsa, Elena-Maria
    Milaciu, Mircea Vasile
    Albu, Adriana
    BALNEO RESEARCH JOURNAL, 2019, 10 (01) : 3 - 7
  • [2] Stimulus dependence of non-steroidal antiinflammatory drug potency in a cellular assay of prostaglandin H synthase-2
    Hulkower, KI
    Otis, ER
    Wernimont, AK
    Bell, RL
    EUROPEAN JOURNAL OF PHARMACOLOGY, 1997, 331 (01) : 79 - 85
  • [3] PHOTOCATALYTIC OXIDATION OF NON-STEROIDAL ANTIINFLAMMATORY DRUGS
    Trousil, V
    Blazkova, Z.
    Muselikova, J.
    Slehova, E.
    Palarcik, J.
    Machalicky, O.
    Cakl, J.
    PROCEEDINGS OF THE 4TH INTERNATIONAL CONFERENCE ON CHEMICAL TECHNOLOGY, 1ST EDITION, 2016, : 440 - 444
  • [4] Cardio-renal safety of non-steroidal anti-inflammatory drugs
    Radi, Zaher A.
    Khan, K. Nasir
    JOURNAL OF TOXICOLOGICAL SCIENCES, 2019, 44 (4-6) : 373 - 391
  • [5] Impact of Non-steroidal Anti-inflammatory Drug Administration for 12 Months on Renal Function
    Hayashi, Kazuhiro
    Miki, Kenji
    Kajiyama, Hiroshi
    Ikemoto, Tatsunori
    Yukioka, Masao
    FRONTIERS IN PAIN RESEARCH, 2021, 2
  • [6] Non-steroidal mineralocorticoid receptor antagonism for the treatment of cardiovascular and renal disease
    Bramlage, Peter
    Swift, Stephanie L.
    Thoenes, Martin
    Minguet, Joan
    Ferrero, Carmen
    Schmieder, Roland E.
    EUROPEAN JOURNAL OF HEART FAILURE, 2016, 18 (01) : 28 - 37
  • [7] Compartmental study of rat renal prostaglandin synthesis during development
    FernandezTome, MD
    DAntuono, C
    Kahane, VL
    Speziale, EHS
    SterinSpeziale, NB
    BIOLOGY OF THE NEONATE, 1996, 70 (04): : 235 - 245
  • [8] Prevention of αIIbβ3 activation by non-steroidal antiinflammatory drugs
    Domínguez-Jiménez, C
    Díaz-González, F
    González-Alvaro, I
    Cesar, JM
    Sánchez-Madrid, F
    FEBS LETTERS, 1999, 446 (2-3) : 318 - 322
  • [9] Use of non-steroidal anti-inflammatory drugs in renal transplant patients: A retrospective study
    Sridharan, Kannan
    Shah, Shamik
    INTERNATIONAL JOURNAL OF RISK & SAFETY IN MEDICINE, 2023, 34 (04) : 379 - 386
  • [10] Non-steroidal anti-inflammatory drugs and renal response to exercise: a comparison of indomethacin and nabumetone
    Olsen, NV
    Jensen, NG
    Hansen, JM
    Christensen, NJ
    Fogh-Andersen, N
    Kanstrup, IL
    CLINICAL SCIENCE, 1999, 97 (04) : 457 - 465