Dynamics of adenylate cyclase desensitization during long-term exposure to the hormone

The dependence of adrenal gland adenylate cyclase desensitization on the dose of in vivo injected ACTH, the time of occurrence and duration of the enzyme refractory period and the dependence of desensitization on the number of ACTH injections were analyzed. The experiments were carried out on guinea pigs injected with prolonged action preparations of ACTH (4 and 6 units) daily for 1-6 days. Intramuscular injections of ACTH caused adenylate cyclase refraction to the repeated action of the hormone. The effect of desensitization was the most conspicuous within the first few hours after hormone injection. The decrease of adenylate cyclase sensitivity and the duration of this effect were found to depend on the ACTH dose as well as on the number of injections. It has been shown for the first time that a single in vivo injection of 0.9% NaCl causes short-term desensitization of adenylate cyclase to the repeated action of much higher doses of ACTH in vitro, presumably due to endogenous ACTH release in response to weak stress exposure. The periodicity of changes in adenylate cyclase sensitivity upon prolonged hormone administration is discussed. Sensitization of the enzyme upon daily short-term exposure to physiological doses of ACTH (administration of 0.9% NaCl for 6 days) was revealed.     

Structural identity of active sites of RNases

It is known that the affinity of all nucleoside monophosphate isomers for RNAase active sites increases in the following order: 5'-NMP----3'-NMP----2'-NMP, irrespective of the RNAase type (pyrimidine-specific, guanine-specific or non-specific) and stage of activity (transferase, hydrolase). It is known also that the nucleotides with the same degree of isomerism have substantially the same conformation. It was thus supposed that the structure of active sites of RNAase has common features with a closer similarity in case of pyrimidine-specific (EC 3.1.4.22), guanine-specific (EC 3.1.4.8) and non-specific (EC 3.1.4.23) RNAases.     

Olfactory coding by lepidopterous larvae

Extracellular electrophysiological recording from olfactory receptors in the antennae of tobacco hornworm larvae (Manduca sexta (Johan.)) has revealed that cells respond differentially to different odors by changing latency, rate of increase of frequency of firing, rate of adaptation, and alternation of frequency increase and decrease. The resulting temporal patterns of spike activity could function as a code to allow for discrimination among various plant odors.

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Zusammenfassung Extrazelluläre elektrophysiologische Erregungsableitungen von Geruchsrezeptoren in den Antennen von Tabakschwärmer-Raupen (Manduca sexta (Johan.)) ergaben, daß die Zellen auf verschiedene Duftstoffe unterschiedlich mit Änderung der Latenzzeit, der Zunahmerate der Erregungsfrequenz, der Anpassungsrate sowie der Änderung der Frequenz-Zunahme und-Abnahme reagieren. Die sich daraus ergebenden Zeitmuster der Spike-Aktivität könnten als Code dienen und so die Unterscheidung zwischen verschiedenen Pflanzendüften ermöglichen.

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This research was supported by National Science Foundation Grant GB-1472.     

Bacterial oxidation of polythionates: determination of tetrathionate with an ion-selective electrode.

A commercially available ion-selective electrode for nitrate was used to continuously monitor tetrathionate oxidation by Thiobacillus dentrificans. The electrode was much more sensitive to tetrathionate than to nitrate. The same electrode could also be used for the determination of trithionate.