Enhancement by caffeine of sister-chromatid exchange frequency induced by antineoplastic agents in human lymphocytes.

The SCE frequency induced by Thiotepa and the effect of this antineoplastic drug in combination with caffeine have been studied in cultures of human peripheral blood. Caffeine was found to enchance SCE and breakage frequencies induced by Thiotepa in human lymphocytes.     

Enhancement by caffeine of the frequency of anaphase-telophase chromatin bridges induced by triethylenemelamine (TEM)

Summary Treatment of BHK cells for 8 h with triethylenemelamine (TEM) followed by caffeine for 4 or 8 h, increased the frequency of anaphase-telophase chromatin bridges in relation to controls and TEM-treated cells. These results indicate that TEM-induced chromosome lesions detected as chromatin bridges at anaphase-telophase could be potentiated by caffeine.This work was supported by grants from CIC, CONICET and CAFPTA.     

Long-lasting persistence of elevated sister-chromatid exchange frequencies induced by perinatal benzo(a)pyrene treatment in rat bone-marrow cells

In this work the possibility that a mutagenic factor acting in utero or in the perinatal period might lead to elevated mutagenic rates in bone-marrow cells after a considerable period of time was examined. An aromatic hydrocarbon, benzo(a)pyrene was used as the test substance. Benzo(a)pyrene treatments resulted in significantly higher sister-chromatid exchange (SCE)-frequencies in both fetal and neonatal groups in both sexes, even four months after exposure. In a second experiment we examined whether mutagenic exposure suffered in utero could make the individual more susceptible to mutagenic effects in adulthood. Preliminary results indicate that such a possibility could exist.     

5-Bromodeoxyuridine induced sister chromatid exchange frequencies in primate lymphocytes

Summary Comparisons of SCE frequencies at various BrdUrd concentrations showed significant interspecies differences with human lymphocytes being the most sensitive. I wish to thank S. Noble. A Kirkilionis and D. Lang for their assistance, Dr S.L. Cleland of Connaught Laboratories, Toronto, who provided most of the monkey blood samples and the Metro Toronto Zoo for providing the gorilla blood samples.     

Steroid hormones enhanced sister-chromatid exchange in cultured CHO cells

Summary The influence of steroid hormones on the induction of sister-chromatid exchange (SCE) in cultured CHO cells was studied. It was observed that estradiol-17 , estriol, estrone and ethynyl estradiol treatments enhanced SCE rates compared to the controls. Overall, these compounds produced a dose response effect. The importance of a detailed study on the long-term genetic effects of steroids on mammalian cells is emphasized.This work was supported by NIH-Minority Biomedical Research Support Program (MBRS), Grant No. RR 08124-11. The author is thankful for the technical assistance provided by NIH-MBRS student, Hoang Duong.     

Steroid hormones enhanced sister-chromatid exchange in cultured CHO cells

The influence of steroid hormones on the induction of sister-chromatid exchange (SCE) in cultured CHO cells was studied. It was observed that estradiol-17 beta, estriol, estrone and ethynyl estradiol treatments enhanced SCE rates compared to the controls. Overall, these compounds produced a dose response effect. The importance of a detailed study on the long-term genetic effects of steroids on mammalian cells is emphasized.     

The effects of non-thermal radio frequency radiation on human lymphocytes in vitro

Zusammenfassung Hypotonische Streuungen, die in radiobestrahlten Kulturen menschlicher Lymphozyten Chromosomenaberrationen erkennen liessen, traten dort siebenmal häufiger auf als in unbestrahlten Kulturen; offenbar das Ergebnis einer wärmefreien Bestrahlung. Trotz des Fehlens bedeutender Unterschiede in der DNA-Synthese, der Zellvergrösserung und im mitotischen Index zwischen bestrahlten und unbestrahlten Kulturen kam es zu Aberrationen.     

Fluorescein staining of human lymphocytes induced byEchis colorata venom

Résumé Le venin de l'Echis colorata produit la fluorescence des lymphocytes humains dans un mélange contenant du plasma défibrinogéné et de la fluorescéine. L'effet du venin est causé par l'action conjointe du thrombin produit par le procoagulant du venin et d'un autre facteur, qui peut être une protéase.

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This study was supported by a grant from the Israel Cancer Association.     

Enhancement of ethylemethane sulfonate-induced mutation frequency inDrosophila by dimethyl sulphoxide

Zusammenfassung Die mutagene Wirkung von Aethylenmethansulfonat inDrosophila-Männchen wird durch DMSO um 46% erhöht. DMSO allein kann keine Mutation über die Spontanrate hinaus induzieren.     

Influence of pulsing electromagnetic field on the frequency of sister-chromatid exchanges in cultured mammalian cells

Exposures of Chinese hamster cells to pulsing electromagnetic field (PEMF) with 0.18-2.5 mT did not influence the baseline frequency of sister-chromatid exchanges (SCE). The results suggest that PEMF with the magnetic intensity examined does not interfere with DNA replication nor produce DNA lesions, thereby leading to an increased frequency of SCE.     

Influence of pulsing electromagnetic field on the frequency of sister-chromatid exchanges in cultured mammalian cells

Summary Exposure of Chinese hamster cells to pulsing electromagnetic field (PEMF) with 0.18–2.5 mT did not influence the baseline frequency of sister-chromatid exchanges (SCE). The results suggest that PEMF with the magnetic intensity examined does not interfere with DNA replication nor produce DNA lesions, thereby leading to an increased frequency of SCE.     

Zinc ions block the intracellular calcium release induced by caffeine in guinea-pig taenia caeci

Zn²⁺ in low concentrations (0.005–0.1 mM) inhibited the transient contractions in response to caffeine (25 mM) in a dose-dependent manner in smooth muscle of intact guinea-pig taenia caeci. At Zn²⁺ concentrations higher than 0.1 mM, caffeine did not elicit any response. After saponin-treatment of the fibres, which leaves the Ca²⁺ storage sites intact, caffeine contraction was completely inhibited by Zn²⁺ at a relatively low concentration (0.03 mM). However, in Triton-X-100-treated fibres, in which the Ca²⁺ release sites are destroyed, the contraction could be induced in the presence of Zn²⁺ by an increase in Ca²⁺. In conclusion, Zn²⁺ can block the intracellular Ca²⁺ release from caffeine-sensitive release sites in taenia caeci.