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C A Muller

Publications and source records attributed to C A Muller.

39 records · Page 3Linked to original sources

Studies in search of a suitable experimental insect model for xenodiagnosis of hosts with Chagas' disease. 2 Attempts to upgrade the reliability and the efficacy of xenodiagnosis in chronic Chagas' disease.

In order to upgrade the reliability of xenodiagnosis, attention has been directed towards population dynamics of the parasite, with particular interest for the following factors: 1. Parasite density which by itself is not a research objective, but by giving an accurate portrayal of parasite development and multiplication, has been incorporated in screening of bugs for xenodiagnosis. 2. On the assumption that food availability might increase parasite density, bugs from xenodiagnosis have been refed at biweekly intervals on chicken blood. 3. Infectivity rates and positives harbouring large parasite yields were based on gut infections, in which the parasite population comprised of all developmental forms was more abundant and easier to detect than in fecal infections, thus minimizing the probability of recording false negatives. 4. Since parasite density, low in the first 15 days of infection, increases rapidly in the following 30 days, the interval of 45 days has been adopted for routine examination of bugs from xenodiagnosis. By following the enumerated measures, all aiming to reduce false negative cases, we are getting closer to a reliable xenodiagnostic procedure. Upgrading the efficacy of xenodiagnosis is also dependent on the xenodiagnostic agent. Of 9 investigated vector species, Panstrongylus megistus deserves top priority as a xenodiagnostic agent. Its extraordinary capability to support fast development and vigorous multiplication of the few parasites, ingested from the host with chronic Chagas' disease, has been revealed by the strikingly close infectivity rates of 91.2% vs. 96.4% among bugs engorged from the same host in the chronic and acute phase of the disease respectively (Table V), the latter comporting an estimated number of 12.3 x 10(3) parasites in the circulation at the time of xenodiagnosis, as reported previously by the authors (1982).

Animals↗

Regional myocardial ischemia: characterization of temporal, transmural and lateral flow interfaces in the porcine heart.

The three-dimensional distribution of coronary flow and tissue adenosine triphosphate was characterized in the anaesthetized open pig chest after 10, 15, 30, 45, 60 and 120 min of coronary artery ligation. Radioactive microspheres were given at the onset (153-gadolinium) and end (113-tin) of ischemia. A simultaneous multiple biopsy device was used to obtain 50 contiguous transmural biopsies from each heart over an area (40 mm X 28 mm) of tissue which incorporated the centre of the ischemic zone, a lateral interface of injury and normally perfused tissue. Frozen biopsies were lyophilized, subfractionated into 2 mm transmural sections, and taken for radioactive counting. There was little or no detectable collateral flow in the ischemic zone. There was a sharp lateral flow interface which fell from 2.2 +/- 0.04 mL/min/g in normally perfused tissue to less than 2% of this value over a transition zone of less than 2 mm width. Myocardial adenosine triphosphate content showed a similar sharp interface and was severely depressed throughout the ischemic zone at all the ischemic times studied. During the 2 h ischemic period there was no increase in flow to any part of the ischemic zone and there was no change in the position, or sharpness, of the lateral interface. The absence of either lateral or transmural borderzones of intermediate injury in the pig makes pharmacological infarct size limitation highly improbable in this species.

Adenosine Triphosphate↗