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1.
Article in English | MEDLINE | ID: mdl-8951993

ABSTRACT

Cyclosporine (CsA) (37.4 mumol/kg per day for 7 days) treated female Wistar rats exhibited significantly decreased creatinine clearance (Ccr) and body weight loss (BWL), but had neither proteinuria (PU) nor alteration in their urine volume (V). Light microscopic (LM) sections of rat kidneys showed that all kidneys were affected by lesions, mainly diffuse vacuolization. These changes were associated with decreased urinary excretion ratios of 6-ketoprostaglandin F1 alpha to thromboxane B2 (6kPGF1 alpha/TXB2) and prostaglandin E2 to TXB2 (PGE2/TXB2). When OKY-046, a TXA2-synthetase inhibitor or nifedipine (NFD), a calcium channel blocker and an antagonist of endotheline (ET), were administered in addition to CsA, they restored Ccr and increased urine V but they did not prevent BWL. LM sections showed that only 5 or 7 out of 9 kidneys of animals were affected, respectively. These changes were associated with prevention of the diminished ratios of urinary PGE2/TXB2 and 6kPGF1 alpha/TXB2 mainly in the OKY-046 treated animals. In conclusion, our results suggest that inhibitors of TXA2 or antagonists and/or inhibitors of endothelin play a protective role in the development of the dysfunction induced by CsA. However, the protection observed using OKY-046 and NFD did not reach that obtained by evening primrose oil (EPO) or Ketanserine (KTS), substances which prevented the fall of Ccr and BWL. Furthermore, with these protective agents only 5 out of 9 kidneys were affected and the lesions were of minor importance.


Subject(s)
Calcium Channel Blockers/therapeutic use , Cyclosporine/toxicity , Enzyme Inhibitors/therapeutic use , Immunosuppressive Agents/toxicity , Methacrylates/therapeutic use , Nifedipine/therapeutic use , Renal Insufficiency/prevention & control , Animals , Creatinine/pharmacokinetics , Drug Interactions , Eicosanoids/urine , Fatty Acids, Essential/therapeutic use , Female , Ketanserin/therapeutic use , Kidney Function Tests , Kidney Tubules/pathology , Linoleic Acids , Metabolic Clearance Rate , Oenothera biennis , Plant Oils , Rats , Rats, Wistar , gamma-Linolenic Acid
2.
Nephron ; 70(2): 249-54, 1995.
Article in English | MEDLINE | ID: mdl-7566312

ABSTRACT

Cyclosporine (CsA)-treated female Wistar rats, in dose of 37.5 microM (45 mg)/kg/day for 7 days, exhibited significantly decreased creatinine clearance (Ccr), and provoked body weight loss (BWL), which is consistent with the development of nephrotoxicity (NT). Urine volume (V) did not change and proteinuria (PU) was not provoked. These changes were associated with significantly diminished ratios of urinary PGE2/TXB2 and 6kPGF1 alpha/TXB2 excretions. Light-microscopic (LM) sections of rat kidneys showed that all kidneys were affected but the lesions (mainly diffuse vacuolization) were reversible. When CsA-treated animals were pretreated with ketanserine (KTS), which antagonizes (a) the direct vasoconstrictor effect of serotonin (5-HT), and (b) the amplifying effects of 5-HT on other vasoactive substances (such as noradrenaline (NA), alpha 1-receptors, histamine, H2 receptors, and prostaglandin F2 alpha), Ccr and urine volume significantly increased, BWL was partially prevented and the ratios of urinary PGE2/TXB2 and 6kPGF1 alpha/TXB2 excretions were significantly enhanced. LM sections showed that only 5 of 9 rats were affected but the lesions were of less importance. These observations indicate that the NT induced by CsA in our studies was mediated by 5-HT, a potent vasoconstrictor agent, and by the metabolites of arachidonic acid. However, other vasoactive agents and additional mechanisms could also be implicated.


Subject(s)
Cyclosporine/adverse effects , Immunosuppressive Agents/adverse effects , Ketanserin/pharmacology , Kidney/drug effects , Serotonin Antagonists/pharmacology , Animals , Body Weight , Creatinine/urine , Female , Prostaglandins/urine , Proteinuria , Rats , Rats, Wistar , Thromboxane A2/urine
3.
Article in English | MEDLINE | ID: mdl-8146206

ABSTRACT

Administration of cyclosporine (CsA), 37.4 microM (45 mg)/Kg, per day for 7 days, to Wistar rats, induced decreased creatinine clearance (Ccr) and body weight loss (BWL), but it did not induce proteinuria. These changes were associated with enhanced urinary thromboxane B2 (TXB2) and diminished 6-keto-PGF1 alpha (6kPGF1 alpha) and prostaglandin E2 (PGE2) excretions. The augmentation in TXB2 and the decrease in PGs highly diminished the ratios of 6kPGF1 alpha/TXB2 and PGE2/TXB2. In microscopic sections all of the kidneys were affected to variable degrees. When CsA was administered to animals fed for 70 days, prior to the experiment, on standard chow (SC) containing evening primrose oil (EPO) or fish oil (FO), 1% and 10% respectively (EPO contained 9% gamma-linolenic acid (GLA) and FO 5.6% eicosapentaenoic acid (EPA)), the nephrotoxic effect of CsA was partially prevented. These changes were accompanied by increased ratios of urinary 6kPGF1 alpha/TXB2 and PGE2/TXB2 excretions. Light microscopic (LM) studies showed that rats' kidneys fed on SC containing EPO or FO were not always affected and the lesions were of minor importance. In conclusion, these results suggest that EPO (GLA) and FO (EPA) could play a beneficial role in the development or the modulation of the renal syndrome induced by CsA.


Subject(s)
Cyclosporine/antagonists & inhibitors , Cyclosporine/toxicity , Eicosapentaenoic Acid/pharmacology , Kidney/drug effects , gamma-Linolenic Acid/pharmacology , 6-Ketoprostaglandin F1 alpha/urine , Animals , Creatinine/metabolism , Dinoprostone/urine , Fatty Acids, Essential/pharmacology , Fish Oils/pharmacology , Kidney/pathology , Kidney/physiopathology , Linoleic Acids , Oenothera biennis , Plant Oils , Prostaglandins/metabolism , Rats , Rats, Wistar , Thromboxane B2/urine
4.
Article in English | MEDLINE | ID: mdl-1561232

ABSTRACT

Acute renal failure (ARF) induced with large doses of Gentamicin (GM) (an aminoglycoside) was associated with increased urinary TXB (TXA) excretion which provoked a decrease of the ratios of urinary PGE2/TXB2 and 6-keto-PGF1 alpha (PGI2)/TXB2 excretions. Furthermore, as indicated by light microscopy most of the epithelial cells lining the proximal tubules show obvious lesions varying from swelling of their cytoplasm to complete necrosis. Either the inhibitor, OKY-O46, of TXA-synthetase, or volume expansion (VE) with isotonic saline (IS) of the experimental animals diminished urinary TXB excretion which provoked 1) augmentation of the ratios of urinary PGE/TXB and 6-keto-PGF1 alpha/TXB excretions, 2) elevation of creatinine clearance (Ccr) and 3) diminution of proteinuria (PU). This protection against ARF-by OKY-O46 and VE can a can be seen in microscopic sections where necrosis of proximal tubules is almost absent. Only a few proximal tubules show swelling of their epithelial cells and some focal areas of tubule necrosis. We suggest that the metabolites of arachidonic acid (AA), TXA2 a (potent vasoconstrictor agent) and prostaglandins (PGE2 and PGI2), (potent vasodilator factors), play an important role in the development (TXA2) or in the prevention (PGs) of ARF induced by this antibiotic.


Subject(s)
Acute Kidney Injury/chemically induced , Gentamicins/toxicity , Thromboxane A2/biosynthesis , Acute Kidney Injury/metabolism , Acute Kidney Injury/pathology , Animals , Arginine Vasopressin/metabolism , Catecholamines/metabolism , Female , Kidney/drug effects , Kidney/metabolism , Kidney/pathology , Methacrylates/pharmacology , Prostaglandins/metabolism , Rats , Rats, Inbred Strains , Renin-Angiotensin System/drug effects , Thromboxane-A Synthase/antagonists & inhibitors
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