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J Doers

Publications and source records attributed to J Doers.

2 recordsLinked to original sources

Hypoxia and metabolic acidosis in the isolated heart: evidence for synergistic injury.

Although hypoxia and metabolic acidosis have both been shown to impair cardiac function, some workers have suggested that acidosis during a period of hypoxia will actually accelerate physiologic recovery from this insult. To address the interactions of metabolic acidosis and hypoxia further, isolated isovolumic rat hearts were exposed to normal perfusion conditions for 30 min to establish baseline conditions, then either continued normal conditions, metabolic acidosis, hypoxia, or combined acidosis and hypoxia for 30 min and subsequently reperfused under normal perfusion conditions for an additional 30 min. We observed that acidosis + hypoxia impaired recovery of cardiac contraction more than acidosis or hypoxia alone following experimental perfusion. The combination of acidosis and and hypoxia also impaired cardiac energy metabolism more than acidosis or hypoxia alone as assessed by increases in tissue inorganic phosphate during experimental perfusion as well as during reperfusion. These data suggest that during hypoxia, acidosis appears to primarily impair cardiac energy production as we have previously observed in the normoxic isolated rat heart. Therefore, in the intact beating heart, acidosis may not protect from hypoxic injury as has been suggested in simpler systems but may not protect from hypoxic injury as has been suggested in simpler systems but rather may exacerbate at.

Acidosis↗

Isolation of functionally active pleural macrophages.

Pleural fluid provides an easily accessible source of tissue macrophages (MACS). We established a method for retrieval and isolation of these cells. Thirty thoracenteses were performed on patients with the clinical diagnosis of congestive heart failure or malignancy. Within 4 hr of thoracentesis, the specimen was placed on a Ficoll-Hypaque gradient, centrifuged, and the mononuclear cells were isolated. Assessment for total cell count, cell viability, and percentage of cells which were MACS as determined by nonspecific esterase staining was recorded. Pleural MACS were separated by glass adherence. In 24 cases, sufficient cells were available to measure the release of hydrogen peroxide spontaneously and with phorbol myristate acetate (PMA) stimulation. Nine of 24 specimens had spontaneous hydrogen peroxide release. In all cases, stimulation of pleural MACS resulted in a significant increase in the amount of hydrogen peroxide released. We report a simple method for retrieving viable and functionally active pleural macrophages.

Cell Count↗