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1.
Ren Fail ; 21(1): 85-100, 1999 Jan.
Article in English | MEDLINE | ID: mdl-10048120

ABSTRACT

BACKGROUND: Ularitide is a member of the natriuretic peptide family. This hormone exhibits an N-terminal extension by four amino acids compared with atrial natriuretic peptide. Ularitide was shown to exert strong diuretic and natriuretic effects when infused intravenously. Its main action sites are the glomerulum, inducing preglomerular vasodilation and postglomerular vasoconstriction and thereby elevating the glomerular filtration rate, and the tubular system inhibiting Na(+)-reabsorption. In initial uncontrolled clinical trials, this peptide was shown to have beneficial effects in patients suffering from oliguric acute renal failure. METHODS: We conducted a double-blind, placebo-controlled, multicenter, dose-finding trial recruiting 176 patients randomized into 4 different Ularitide doses groups (U5, U20, U40, and U80 ng/kg/min) and a placebo group (U0). Ularitide/placebo infusion was performed for 5 days with half the originally infused dose on day 5. The primary objective of the study was to test various doses of Ularitide in patients suffering from oliguric acute renal failure to avoid mechanical renal replacement therapy during the first 12 hours. FINDINGS: The results indicate that Ularitide does not reduce the incidence of mechanical renal replacement therapy compared with placebo-treated patients during the first 12 h of treatment (U0: 36 (20), U5: 35 (11), U20: 36 (9), U40: 28 (8), U80: 41 (12), (% (n) (p = 0.87)). Diuresis increased in the Ularitide-treated groups and the placebo group after onset of infusion and did not show any significant difference in the first 12 h collection period (U0: 576, U5: 514, U20: 500, U40: 360, U80: 158 ML/12h (Median), (p = 0.16)). INTERPRETATION: In summary, the incidence of mechanical renal replacement therapy in critically ill patients suffering from oliguric acute renal failure could not be altered positively by Ularitide administration according to our protocol. Further prospective clinical trials are needed to answer the question whether a different patient collective or a prophylactic administration of Ularitide are more promising approaches in the clinical setting of oliguric acute renal failure.


Subject(s)
Acute Kidney Injury/drug therapy , Atrial Natriuretic Factor/therapeutic use , Diuretics/therapeutic use , Peptide Fragments/therapeutic use , Acute Kidney Injury/complications , Acute Kidney Injury/physiopathology , Aged , Atrial Natriuretic Factor/administration & dosage , Atrial Natriuretic Factor/adverse effects , Blood Pressure , Blood Urea Nitrogen , Cardiovascular Diseases/etiology , Creatinine/blood , Creatinine/metabolism , Diuretics/administration & dosage , Diuretics/adverse effects , Double-Blind Method , Female , Humans , Hypotension/etiology , Male , Middle Aged , Peptide Fragments/administration & dosage , Peptide Fragments/adverse effects , Renal Replacement Therapy , Time Factors
2.
Curr Opin Nephrol Hypertens ; 5(4): 364-8, 1996 Jul.
Article in English | MEDLINE | ID: mdl-8823536

ABSTRACT

Ularitide is a member of the natriuretic peptide family which is presumably synthesized in the kidney. In physiological experiments a correlation between Ularitide excretion and natriuresis has been found. Ularitide infusions and bolus injections in animals initiated profound diuresis and natriuresis as the most prominent effects. On the basis of findings in in-vitro and in-vivo experiments, Ularitide was used in clinical trials, and the results indicate that it could be a promising new drug to prevent and treat acute renal failure in patients after cardiac surgery and organ transplantation.


Subject(s)
Atrial Natriuretic Factor/pharmacology , Diuretics/pharmacology , Kidney/physiology , Peptide Fragments/pharmacology , Acute Kidney Injury/prevention & control , Amino Acid Sequence , Animals , Atrial Natriuretic Factor/chemistry , Atrial Natriuretic Factor/pharmacokinetics , Atrial Natriuretic Factor/physiology , Atrial Natriuretic Factor/therapeutic use , Cardiac Surgical Procedures , Clinical Trials as Topic , Diuretics/pharmacokinetics , Diuretics/therapeutic use , Humans , Kidney/drug effects , Kidney/physiopathology , Molecular Sequence Data , Muscle Proteins/chemistry , Peptide Fragments/pharmacokinetics , Peptide Fragments/therapeutic use , Postoperative Complications/prevention & control , Receptors, Atrial Natriuretic Factor/physiology , Second Messenger Systems/physiology , Transplantation , Vasodilator Agents/chemistry
3.
Chemosphere ; 31(2): 2611-28, 1995 Jul.
Article in English | MEDLINE | ID: mdl-7663948

ABSTRACT

A method was developed which allows effective searching for information on chemical substances in databases. Several searches for chemicals in bibliographic databases were carried out to analyse the method of indexing chemical names. The recall rates of documents were compared to evaluate information resources as well as searching strategies. Recall rates of documents searched with the CAS Nos. were compared to those searched with substance name. It turned out that searching for substances is most specific and fastest with CAS Nos. They should always be used whenever possible. However, this is not sufficient in many BDs, making an additional search using chemical names necessary. Specific search options that have to be considered for each database are reported.


Subject(s)
Databases, Bibliographic/statistics & numerical data , Information Storage and Retrieval , Pharmaceutical Preparations , Terminology as Topic , Abstracting and Indexing , Information Systems , Models, Chemical , Online Systems
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