Radioimmune, radiobinding and HPLC analysis of 2-5A and related oligonucleotides from intact cells

The enzyme (2-5A synthetase) which synthesizes ppp(A2'p)nA where n=2 to 4 (collectively referred to as 2-5A) is widely distributed in a variety of cells and tissues in amounts which increase response to interferon and vary with growth and hormone status. 2-5A activates a nuclease which inhibits protein synthesis. The non-phosphorylated 'core' of 2-5A ((A2'p)nA, n=2 to 4) can inhibit DNA synthesis and cell growth. Here we describe convenient and sensitive radioimmune (RI) and radiobinding (RB) assays for core and 2-5A. In combination with more satisfactory high performance liquid chromatography (HPCL) methods using reverse-phase C18 columns, these assays have been used to detect core and 2-5A in crude extracts from interferon-treated cells. The novel 2-5A synthetase products NAD2'p5' A2'p5'A and A5'p45'A2'p5'A2'p5'A (ref. 13), which can also be detected using the RB assay, were not found in significant amounts. The natural occurrence of core has not been described previously.     

1,2-di-n-butylhydrazine dihydrochloride carcinogenesis in mice

Summary A solution of 0.0625% 1,2-di-n-butylhydrazine dihydrochloride (1,2-DBH) was given continuously in the drinking water of 6-week-old randomly bred albino Swiss mice for the remainder of their lives. The treatment gave rise to tumors of the lungs, lymphoreticular tissue and kidneys.     

Similar effects of arginine-vasopressin and arginine-vasotocin on permeability of toad skin

Résumé Des crapauds ont été employés pour doser l'action des peptides neurohypophysaires sur la perméabilité de la peau. L'arginine⁸-vasopressine et l'arginine⁸-vasotocine ont en absence de Na⁺ le même effet. Elles augmentent les mouvements de l'eau, à doses variées, et leur action à toutes deux est 2000 fois plus puissante que celle de l'oxytocine. En presence de Na⁺ l'action de l'arginine⁸-vasotocine est 3 fois plus grande que celle de l'arginine⁸-vasopressine. Elles sont respectivement 120 fois et 40 fois plus puissantes que l'oxytocine.     

Approach to a quantitative differentiation between the respiratory effects evoked from the lung stretch and the lung deflation receptors during thoracic compression

Zusammenfassung Die beiden Annahmen, dass sich bei Thoraxkompression die Verminderung der Impulssequenz der Lungendehnungsrezeptoren analog zum Lungenentdehnungsreflex auswirke, und dass sich dessen inspiratorische Atmungseffekte zu jenen des Lungenkollapsreflexes addieren, erscheinen gerechtfertigt. Diese Annahmen ermöglichen eine quantitative Differenzierung zwischen dem respiratorischen Einfluss der Lungendehnungs-und Lungenkollapsrezeptoren bei Thoraxkompression. Damit können die auf die Erregung der Lungenkollapsrezeptoren zu beziehenden Atmungsveränderungen (f,I/E) erstmals isoliert und quantitativ dargestellt werden.

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Presented at the 2nd Meeting of the Swiss Physiological Society, Zürich, 8 November 1969.