Quirks of dye nomenclature. 1. Evans blue

The history, origin, identity, chemistry and use of Evans blue dye are described along with the first application to staining by Herbert McLean Evans in 1914. In the 1930s, the dye was marketed under the name, Evans blue dye, which was profoundly more acceptable than the ponderous chemical name.     

Evans blue treatment promotes blastomere separation and twinning in Lytechinus pictus embryos

Demembraned Lytechinus pictus embryos briefly treated with the dye Evans Blue during the first cleavage division subsequently showed frequent blastomere disengagement leading to development of twinned embryos. Further development of twinned embryos was observed in hanging drops and in batch cultures. The timing of micromere production was disturbed in some twinned embryos, but this disturbance was not correlated with subsequent developmental problems. Many twinned embryos resulting from blastomere separation following Evans Blue treatment developed into small but normal-appearing plutei.     

Differential inhibitory effects of Evans blue on various DNA polymerases

Evans Blue, an anionic dye which has been found to inhibit the replication of human immunodeficiency virus, proved also inhibitory to the DNA polymerases alpha and beta. The mode of inhibition was competitive with respect to the template X primer, and noncompetitive with respect to the deoxynucleoside triphosphate substrates. The inhibitory effect of Evans Blue on DNA polymerases is discussed in relation to that of suramin.     

Heat treatment and viability assessment by Evans blue in cultured Symbiodinium kawagutii cells

Evans blue was used to determine viability in Symbiodinium kawagutii cultures but heat treatments at up to 80°C for 1 h were required for detecting blue-stained dead cells. About 3 h at this temperature was necessary to obtain ~50% blue-stained dead cells, and more than 6 h for 100%. In comparison, Trypan blue showed unusual elevated numbers of viable cells at times when more than 50% cells were dead by Evans blue parameters. Respiration decreased to 17 and 13.2% after 1 and 2 h at 80°C, respectively, and a marginal but still statistically significant 7.5% was scored after 3 h. Thus, cultured S. kawagutii cells were more resistant to heat-induced death than expected, and Evans blue was reliable for assessment of their viability.     

Albumin extravasation rates in tissues of anesthetized and unanesthetized rats

Bovine serum albumin (BSA) labeled with 131I was injected intravenously in chronically prepared, unanesthetized rats and into pentobarbital-anesthetized rats that had received 2 ml 5% BSA to help sustain plasma volume. Initial uptake rates (clearances) in skin, skeletal muscles, diaphragm, and heart (left ventricle) were measured over 1 h. BSA labeled with 125I was injected terminally to correct for intravascular 131I-BSA. Observed clearances were in the following order in both groups of animals: heart much greater than diaphragm approximately equal to skin greater than resting skeletal muscles. Differences between unanesthetized and anesthetized animals were small and inconsistently directed. Our results suggest that the lower albumin clearances reported in the literature for anesthetized rats are not the result of their immobility or any direct effect of anesthesia on albumin transport in these tissues. The lower transport rates appear to result indirectly from changes produced by anesthesia and/or surgery in controllable parameters such as plasma volume and intravascular protein mass.     

Tissue-specific distribution of uncoupling proteins in normal rats and rats with high-fat-diet-induced obesity

Uncoupling proteins (UCPs) are a proton transporter family located in the mitochondrial inner membrane. Thus far, five molecules (UCP1–UCP5) have been identified as members of the UCP family. Recently, UCPs have attracted considerable interest in research on energy metabolism and obesity. However, to date, no study has focused on a comprehensive and systematic evaluation of the tissue-specific distribution of UCPs in obese individuals. Our study presents evidence of differential tissue expression profiles of five isoforms of UCPs in normal and diet-induced obese (DIO) rats using real-time polymerase chain reaction (PCR) analysis. The results clearly show that the tissue-specific expression patterns of individual isoforms between DIO and normal rats are quite distinct, which suggests a close relationship between the alterations in UCP expression and dietary obesity.     

Evans blue as an adjuvant for enhancing delayed hypersensitivity in an experiment

A modified method has been elaborated for induction of delayed type hypersensitivity (DH) in CBA mice with the use of Evans blue (EB) as adjuvant. This model permitted studying the mechanism of DH development, establishing the dependence of DH on the dose of EB, the dose and type of protein antigen, and realizing passive transfer of DH with the aid of splenocytes from active-synthesized mice. EB is a convenient and effective adjuvant for induction and study of the mechanism of DH development.     

Putrescine has hypothermic and antipyretic activity, in rats

Intraperitoneal injection of putrescine induced dose-related hypothermia in rats. The effect was more pronounced at room temperature (22 degrees C) than in a warm environment (30 degrees C), the maximum hypothermia (-2.64 +/- 0.29 degrees C, 30 min. after treatment) being obtained with the dose of 300 mg/Kg and remaining significant throughout 3 hr of observation. Putrescine also had antipyretic activity, as it significantly reduced pyrogen-induced fever at a dose level (100 mg/Kg i.p.) ineffective in causing hypothermia in normal rats. The hypothermic and antipyretic effects of putrescine were not associated with any obvious sign of toxicity.