1991Defense Technical Information Center (DTIC)Requires access

Extension of Oxygen Tolerance in Man. Predictive Studies 6.

Lambertsen, C. J., Matthew Clark

Open publisher page 0 citations

Abstract

In order to determine rates of recovery from different degrees of oxygen poisoning, oxygen exposure periods of 20, 60, or 120 min were systematically alternated with a constant normoxic interval whose duration was also varied systematically in different exposures. Durations of normoxic intervals were selected to provide the same hyperoxic: normoxic ratios for each of the three oxygen exposure periods. This was done to determine whether the toxic events accumulated over a relatively long oxygen exposure (120 min) reversed on return to normoxia at the same rate as those that accumulated during shorter oxygen exposures (60 or 20 min). Intact animal responses to the selected patterns of intermittent exposure were determined at oxygen pressures of 1.5, 2. 0, and 4.0 ATA. This range of oxygen pressures allowed comparison of results obtained at 1.5 and 2.0 ATA, where effects of pulmonary oxygen toxicity were not influenced by concurrent convulsions, with comparable data obtained at 4.0 ATA, where there were prominent interactions between pulmonary and central nervous system effects of oxygen toxicity.

About this research paper

What this paper is about

In order to determine rates of recovery from different degrees of oxygen poisoning, oxygen exposure periods of 20, 60, or 120 min were systematically alternated with a constant normoxic interval whose duration was also varied systematically in different exposures. Durations of normoxic intervals were selected to provide the same hyperoxic: normoxic ratios for each of the three oxygen exposure periods. This was done to determine whether the toxic events accumulated over a relatively long oxygen exposure (120 min) reversed on return to normoxia at the same rate as those that accumulated during shorter oxygen exposures (60 or 20 min). Intact animal responses to the selected patterns of intermittent exposure were determined at oxygen pressures of 1.5, 2. 0, and 4.0 ATA. This range of oxygen pressures allowed comparison of results obtained at 1.5 and 2.0 ATA, where effects of pulmonary oxygen toxicity were not influenced by concurrent convulsions, with comparable data obtained at 4.0 ATA, where there were prominent interactions between pulmonary and central nervous system effects of oxygen toxicity.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

In order to determine rates of recovery from different degrees of oxygen poisoning, oxygen exposure periods of 20, 60, or 120 min were systematically alternated with a constant normoxic interval whose duration was also varied systematically in different exposures. Durations of normoxic intervals were selected to provide the same hyperoxic: normoxic ratios for each of the three oxygen exposure periods. This was done to determine whether the toxic events accumulated over a relatively long oxygen exposure (120 min) reversed on return to normoxia at the same rate as those that accumulated during shorter oxygen exposures (60 or 20 min). Intact animal responses to the selected patterns of intermittent exposure were determined at oxygen pressures of 1.5, 2. 0, and 4.0 ATA. This range of oxygen pressures allowed comparison of results obtained at 1.5 and 2.0 ATA, where effects of pulmonary oxygen toxicity were not influenced by concurrent convulsions, with comparable data obtained at 4.0 ATA, where there were prominent interactions between pulmonary and central nervous system effects of oxygen toxicity.

Key concepts: Oxygen, Oxygen toxicity, Hyperoxia, Toxicity, Chemistry, Apparent oxygen utilisation, Limiting oxygen concentration, Anesthesia

Related papers

Back to paper searchBrowse research topicsOriginal source
Extension of Oxygen Tolerance in Man. Predictive Studies 6. — Research Paper | ScholarLens