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Biomedical subjects

S M Kutas

Publications and source records attributed to S M Kutas.

3 recordsLinked to original sources

Short-term effects of ecadotril in dogs with induced congestive heart failure.

OBJECTIVE: To evaluate short-term hemodynamic effects of ecadotril in a model of congestive heart failure in dogs. ANIMALS: 6 conscious adult male dogs. PROCEDURES: Instruments were placed in dogs to measure left ventricular, aortic, and atrial blood pressures. Heart failure was induced by repeated coronary embolization with latex microspheres. Four times, and in random order, dogs were given vehicle or active drug (3, 10, or 30 mg/kg of body weight) orally. Hemodynamic variables, urine flow, and urinary electrolyte excretion were measured before and 30, 90, and 150 minutes, and 10 and 21 hours after drug administration. RESULTS: Changes in urine flow, heart rate, mean arterial pressure, or peak positive and negative rate of change in ventricular pressure were not apparent. Urinary sodium excretion significantly increased in response to the low and high doses of ecadotril but not in response to the 10 mg/kg dose. Left ventricular end diastolic pressure (LVEDP) consistently decreased in dose- and time-dependent manner. Maximal group-averaged reductions in LVEDP were 5.2, 8.1, and 10 mm Hg for the low, middle, and high doses, respectively. The magnitude of the decrease in LVEDP was not related to cumulative change in urine flow. CONCLUSIONS AND CLINICAL RELEVANCE: Orally administered ecadotril reduced left ventricular filling pressures in these dogs by a mechanism that does not require a substantial diuretic effect. Ecadotril may be effective for alleviating clinical signs in dogs with left-sided heart failure and may be particularly beneficial for use in dogs that are refractory to traditional diuretic therapy.

Animals↗

Suppression of mouse skin allograft rejection by protein A-Yersiniae V antigen fusion peptide.

V antigen is an established virulence factor of Yersinia pestis, the causative agent of bubonic plague. Injection of homogenous staphylococcal protein A-V antigen fusion peptide into mice was previously found to suppress tumor necrosis factor-alpha and interferon-gamma necessary for generation of protective granulomas. Here, we show that BALB/c mice receiving daily intraperitoneal injections of 100 microg of control protein A initiated rejection of C57BL/6 mouse tail skin grafts after 6.2+/-1.1 days. This time doubled to 12.2+/-1.4 days upon similar administration of protein A-V antigen fusion peptide (P<0.001); times of total allograft retention remained constant. This finding indicates that V antigen can postpone inflammation known to be associated with recognition and destruction of foreign tissue by T lymphocytes.

Animals↗

Distinct differences in the requirements for ribonucleoprotein complex formation on differentially regulated pre-edited mRNAs in Trypanosoma brucei.

Incubation of synthetic pre-edited mRNAs with extracts of Trypanosoma brucei mitochondria results in a family of specific, stable ribonucleoprotein (RNP) complexes that can be visualized by non-denaturing gel electrophoresis. We compared complexes that form with a substrate corresponding to the ATPase 6 (A6) pre-mRNA 3' region that is edited in both bloodstream and procyclic forms with a substrate corresponding to the 5' end of apocytochrome b (CYb) pre-mRNA that is edited only in procyclic (insect) forms. Four to five complexes are detected with both substrates and are specific since competition with homologous but not heterologous substrates prevents their formation. Formation of the CYb complex, however, is more sensitive to heterologous RNAs. In addition, the A6 substrate is more effective at preventing formation of CYb complexes than the converse. CYb complex formation is also more sensitive to divalent cation and salt concentrations and formation of one A6 component has a temperature optimum of 37 degrees C while that of CYb is 27 degrees C.

Adenosine Triphosphatases↗