The increasing application of silver nanoparticles (AgNPs) has been raising concerns about their potential adverse effects to human and the environment. However, the knowledge on the systemic toxicity of AgNPs in mammalian systems is still limited. The present study investigated the toxicity of PVP-coated AgNPs in rats treated with repeated oral administration, and compared that with equivalent dose of AgNO . Specifically, one hundred male and female rats were orally administrated with particulate or ionic forms of silver (Ag) separately at doses of 0.5 and 1 mg kg body weight daily for 28 days. The results reveal no significant toxic effects of AgNPs and AgNO up to 1 mg kg body weight, with respect to the body weight, organ weight, food intake, and histopathological examination. Ag distribution pattern in organs of rats treated with AgNPs was similar to that of AgNO treated rats, showing liver and kidneys are the main target organs followed by testis and spleen. The total Ag contents in organs were significantly lower in the AgNPs treated rats than those in the AgNO treated rats. However, the comparisons between AgNPs and AgNO treatments further indicated more potent of AgNPs in biochemical and hematological parameters in rats, including red blood cell count (RBC), platelet count (PLT), white blood cell count (WBC) and aspartate transaminase (AST). Results of this study suggested that particulate Ag at least partially contributed to the observed toxicity of AgNPs, and both ionic and particulate Ag should be taken into consideration in toxicological evaluation of AgNPs. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 609-618, 2017.
Pesticide toxicity may be modified by a number of co-occurring environmental and ecological stressors. Coexposure to predator cues has been shown to potentiate and/or synergize toxicity of pesticides. However, the mechanisms behind these interactions are not well understood. Here we examine the effects of fish predator (bluegill, Lepomis macrochirus) cues on toxicity of five different pesticides to the freshwater cladoceran, Ceriodaphnia dubia. The purpose for examining patterns among pesticides was to test the idea that the mechanism of the interaction could be explained by a general stress response; that is, the interaction patterns would be similar regardless of the pesticide's mechanism of action [MOA]). Acute 96-h concentration-response experiments were conducted for pesticides with and without fish cues. Predator cues influenced the toxicity of pesticides and the interaction patterns varied among pesticides. Fipronil exhibited a synergistic interaction, while predator cues interacted antagonistically for bifenthrin and thiacloprid. Other compounds previously reported to potentiate toxicity (malathion) were found to act additively. The results demonstrate that factors such as pesticide bioavailability, K(OC) , and exposure concentration may be important for predicting the occurrence of these interactions and that patterns were not consistent among pesticides varying in MOA. Predator stress is an important component for structuring communities and ecosystem processes. Fully understanding how this process may interact with organic contaminants may best be achieved by examination at toxicokinetic and toxicodynamic scales.
The toxicity of several agricultural chemicals to aquatic invertebrates has been shown to be temperature-dependent, but the role of daily temperature variation has rarely been examined. The authors simulated a natural daily temperature pattern (a fluctuating cycle of 21 °C to 31 °C over a 24-h period) based on field-collected data from Southern High Plains wetlands (TX, USA) and conducted a series of experiments comparing responses from this exposure scenario to a constant exposure at 24 ± 1 °C. Results indicate alterations in pesticide toxicity under the fluctuating temperature regime compared with that of the constant temperature exposure. There was a significant interaction of temperature regime and bifenthrin on Chironomus dilutus survival, and C. dilutus ash-free dry mass was lower in the fluctuating temperature treatment. The 10-d median lethal concentration (LC50) for Hyalella azteca exposed to chlorothalonil was lower under the fluctuating temperature regime compared with the constant temperature regime. For Daphnia magna exposed to malathion, the main effects of temperature regime and malathion were observed on cholinesterase activity. The present study demonstrates how environmentally relevant daily temperature variation influences contaminant effects on aquatic invertebrates.
This study was carried out to test the feasibility of enhancing embryo production in vivo and in vitro by immunoneutralisation against inhibin or follistatin. In Experiment 1, multi-parity buffaloes were assigned into three groups: High group (n=8), which received one primary (2mg) and two booster (1mg) vaccinations (28-day intervals) with a recombinant inhibin α subunit in 1 mL of white oil adjuvant; Low group (n=8), which received half that dose; and Control group (n=7), which received only adjuvant. Immunisation against inhibin stimulated development of ovarian follicles. Following superovulation and artificial insemination, inhibin-immunised buffaloes had more developing follicles than the Control buffaloes. The average number of embryos and unfertilised ova (4.5±0.6, n=6) in the High group was higher (P<0.05) than in the Control group (2.8±0.6, n=5) and was intermediate (4.1±0.7, n=7) in the Low group. The pooled number of transferable embryos of the High and Low groups (3.2±0.5, n=13) was also higher (P<0.05) than that (1.6±0.7, n=5) of the controls. The immunised groups also had higher plasma concentrations of activin, oestradiol and progesterone. In Experiment 2, the addition of anti-inhibin or anti-follistatin antibodies into buffalo oocyte IVM maturation medium significantly improved oocyte maturation and cleavage rates following parthenogenic activation. Treatment with anti-follistatin antibody also doubled the blastocyst yield from activated embryos. These results demonstrated that immunisation against inhibin stimulated follicular development, enhanced oocyte quality and maturation competence, yielded more and better embryos both in vivo and in vitro.
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