The effect of bovine myelin basic protein on uptake and release of H3-labelled 5-hydroxytryptamine,L-noradrenalin and γ-aminobutyric acid in rat cortex slices

Summary At concentrations above 10^–5 M myelin basic protein (MBP) induced a small inhibition of the uptake of H³-5HT and H³-NA into rat cortex slices. Release of 5HT, NA and Gaba was not affected by 10^–5 M MBP.Acknowledgment. The authors wish to thank W. Bucher for the preparation of MBP.     

Relationship between the structure of chloramphenicol and its action upon peptide synthetase

Zusammenfassung Zusammenhänge zwischen Struktur und Wirkung bei Chloramphenicol führen zu der Hypothese, dass das Antibiotikum die Peptidsynthetase der Ribosome dadurch hemmt, dass es den Peptidylpartner der Reaktion antagonisiert. Im Einklang damit steht, dass Chloramphenicol sich spezifisch an Ribosome bindet und selektiv die Elongationsphase der Proteinsynthese hemmt.     

Sarcosine dehydrogenase activity in liver mitochondria of infant and adult rats

Zusammenfassung Die Aktivität der Sarcosinedehydrogenase in Lebermitochondrien 7tägiger Ratten ist um 50% kleiner als in adulten Tieren. Dieser Unterschied ist nicht durch das Elektrontransportflavoprotein limitiert und kann auch nicht durch eine Änderung in dem relativen Wert der löslichen Proteine in den Mitochondrien erklärt werden.     

Cellular inactivation by ultrasound

The lethal effect of ultrasound (US) on mammalian cells has received relatively little attention. Understandably, potential genetic aspects of US have been of prime concern to physicians who use US as a diagnostic tool; at the average power densities involved (<1 W cm(-2)) little, if any cell killing is to be expected. There have been sporadic attempts to use higher intensities ( approximately 1 W cm(-2)) as a treatment modality in cancer therapy, but those experiments seem to have been based on inadequate cellular studies. The effects of US usually were evaluated in terms of morphological criteria rather than on quantitative determination of the loss of viability as measured by colony formation. There are few reports of the effects of US on survival of mammalian cells, and none specifically examine hyperthermic interaction. With the increased interest in hyperthermia for tumour therapy, attention has been directed towards the use of ultrasound to achieve tumour heating. In preliminary experiments in which US was used to heat the EMT6 sarcoma and KHJJ carcinoma in mice, we found a high percentage of tumour cures with short (approximately 30 min) treatments at temperatures (43-44 degrees C) where in vitro results of hyperthermia-induced cell killing would not have led to a prediction of any cures. We therefore initiated an investigation of the effects of US on survival of Chinese hamster cells to see if direct cell killing by US could explain our in vivo results, or, as in the case of radiofrequency (RF) electromagnetic heating, we would be forced to invoke host response(8). In particular, we examined the thermal and non-thermal components of cellular inactivation by US. We report here that there is a definite non-thermal cytotoxic effect of US. Its relative contribution to cell killing is a highly nonlinear function of the temperature of the cellular milieu. The survival curves show clearly that, beyond an initial threshold, small changes in temperature and/or US intensity can give rise to impressive changes in survival values. The threshold nature of the data strongly suggests that by means of overlapping beams, ultrasound energy could be delivered to tumour tissue to achieve massive cell killings while sparing normal tissue outside the tumour volume to a degree far exceeding that of conventional techniques.