Passage and reproductive activity of fishes in the Igarapava fish ladder,Grande River,Southeastern Brazil

We sampled fishes within the vertical‐slot Igarapava fish ladder (IFL), Grande River, southeastern Brazil, and immediately downstream IFL in 12 field trips from February 2000 to December 2002. A total of 1145 fishes belonging to 13 families and 39 species were captured. The most abundant species captured within the IFL, in order of abundance were: Pimelodus maculatus, Metynnis maculatus, Astyanax altiparanae, Hypostomus spp., Leporinus octofasciatus, Salminus hilarii, Leporinus elongatus, Leporinus friderici, Schizodon nasutus and Prochilodus lineatus. Size distribution of the most abundant fishes captured downstream or within the IFL was similar indicating no constraints to adult fish to ascend the IFL. Except P. maculatus, the number of migratory species captured in the IFL and downstream the IFL were very low. Some of the so‐called sedentary species were collected in the IFL indicating that they possess an innate behaviour to migrate. Juveniles of P. lineatus and P. maculatus were captured ascending the IFL implying a dispersal behaviour. Gonadal analyses of the fishes captured in the reproductive season showed that the overall number of reproductive active fishes (which included fish in maturation, mature and spawned/spent) surpassed those non‐active. Thus, the IFL offers upstream passage for juveniles, some of the so‐called sedentary species, as well as fishes in reproductive migration. Copyright © 2009 John Wiley & Sons, Ltd.     

The Use of Infrared Thermography as a Novel Approach for Real-Time Validation of PCR Thermocyclers

Validation of PCR thermocycler performance is crucial to obtain reliable results. In this study, infrared (IR) thermography was evaluated as a novel validation tool. After stabilisation, no significant difference in the temperatures recorded using thermography and a reference block-based system was found. By employing IR thermography, information about the length of the time until temperature stabilisation in the sample could be obtained. This study shows the potential of using IR thermography for validation of thermocyclers.     

Solitary Foraging in the Ancestral South American Ant, <Emphasis Type="Italic">Pogonomyrmex vermiculatus</Emphasis>. Is it Due to Constraints in the Production or Perception of Trail Pheromones?

Several North American species of Pogonomyrmex harvester ants exhibit group foraging, whereas South American species are exclusively solitary foragers. The composition of the secretions of the poison and Dufour glands in the South American species, Pogonomyrmex vermiculatus, were analyzed, and the secretions and their components were tested as trail pheromones in laboratory bioassays. The major compounds in the poison gland were the alkylpyrazines, 2,5-dimethylpyrazine, 2,3,5-trimethylpyrazine, and 3-ethyl-2,5-dimethylpyrazine. The Dufour gland contained five alkanes, from tridecane to heptadecane, with pentadecane being most abundant. In behavioral bioassays, poison gland extracts and the mixture of pyrazines produced a trail pheromone effect, whereas the Dufour gland extracts and the alkanes had no effect on ant locomotion. We conclude that group foraging in P. vermiculatus does not arise from the inability to produce or detect possible pheromones, but rather, from physiological and/or ecological factors.     

Dichloroacetate Radiosensitizes Hypoxic Breast Cancer Cells

Mitochondrial metabolism is an attractive target for cancer therapy. Reprogramming metabolic pathways can potentially sensitize tumors with limited treatment options, such as triple-negative breast cancer (TNBC), to chemo- and/or radiotherapy. Dichloroacetate (DCA) is a specific inhibitor of the pyruvate dehydrogenase kinase (PDK), which leads to enhanced reactive oxygen species (ROS) production. ROS are the primary effector molecules of radiation and an increase hereof will enhance the radioresponse. In this study, we evaluated the effects of DCA and radiotherapy on two TNBC cell lines, namely EMT6 and 4T1, under aerobic and hypoxic conditions. As expected, DCA treatment decreased phosphorylated pyruvate dehydrogenase (PDH) and lowered both extracellular acidification rate (ECAR) and lactate production. Remarkably, DCA treatment led to a significant increase in ROS production (up to 15-fold) in hypoxic cancer cells but not in aerobic cells. Consistently, DCA radiosensitized hypoxic tumor cells and 3D spheroids while leaving the intrinsic radiosensitivity of the tumor cells unchanged. Our results suggest that although described as an oxidative phosphorylation (OXPHOS)-promoting drug, DCA can also increase hypoxic radioresponses. This study therefore paves the way for the targeting of mitochondrial metabolism of hypoxic cancer cells, in particular to combat radioresistance.     

Cyp1 Inhibition Prevents Doxorubicin-Induced Cardiomyopathy in a Zebrafish Heart-Failure Model

Doxorubicin is a highly effective chemotherapy agent used to treat many common malignancies. However, its use is limited by cardiotoxicity, and cumulative doses exponentially increase the risk of heart failure. To identify novel heart failure treatment targets, a zebrafish model of doxorubicin-induced cardiomyopathy was previously established for small-molecule screening. Using this model, several small molecules that prevent doxorubicin-induced cardiotoxicity both in zebrafish and in mouse models have previously been identified. In this study, exploration of doxorubicin cardiotoxicity is expanded by screening 2271 small molecules from a proprietary, target-annotated tool compound collection. It is found that 120 small molecules can prevent doxorubicin-induced cardiotoxicity, including 7 highly effective compounds. Of these, all seven exhibited inhibitory activity towards cytochrome P450 family 1 (CYP1). These results are consistent with previous findings, in which visnagin, a CYP1 inhibitor, also prevents doxorubicin-induced cardiotoxicity. Importantly, genetic mutation of cyp1a protected zebrafish against doxorubicin-induced cardiotoxicity phenotypes. Together, these results provide strong evidence that CYP1 is an important contributor to doxorubicin-induced cardiotoxicity and highlight the CYP1 pathway as a candidate therapeutic target for clinical cardioprotection.