Effect of Different Combinations of Cryoprotectants on In Vitro Maturation of Immature Buffalo (Bubalus bubalis) Oocytes Vitrified by Straw and Open‐Pulled Straw Methods

This study was designed to evaluate effects of different combinations of cryoprotectants on the ability of vitrified immature buffalo oocytes to undergo in vitro maturation. Straw and open‐pulled straw (OPS) methods for vitrification of oocytes at the germinal vesicle stage also were compared. The immature oocytes were harvested from ovaries of slaughtered animals and were divided into three groups: (i) untreated (control); (ii) exposed to cryoprotectant agents (CPAs); or (iii) cryopreserved by straw and OPS vitrification methods. The vitrification solution (VS) consisted of 6 m ethylene glycol (EG) as the standard, control vitrification treatment, and this was compared with 3 m EG + 3 m dimethyl sulfoxide (DMSO), 3 m EG + 3 m glycerol, and 3 m DMSO + 3 m glycerol. Cryoprotectants were added in two steps, with the first step concentration half that of the second (and final) step concentration. After warming, oocyte samples were matured by standard methods and then fixed and stained for nuclear evaluation. Rates of MII oocytes exposed to CPAs without vitrification were lower (54.3 ± 1.9% in EG, 47.5 ± 3.4% in EG + DMSO, 36.8 ± 1.2% in EG + glycerol and 29.9 ± 1.0% in DMSO + glycerol; p < 0.05) than for the control group (79.8 ± 1.3%). For all treatments in each vitrification experiment, results were nearly identical for straws and OPS, so all results presented are the average of these two containers. The percentages of oocytes reaching telophase‐I or metaphase‐II stages were lower in oocytes cryopreserved using all treatments when compared with control. However, among the vitrified oocytes, the highest maturation rate was seen in oocytes vitrified in EG + DMSO (41.5 ± 0.6%). Oocytes cryopreserved in all groups with glycerol had an overall low maturation rate 19.0 ± 0.6% for EG + glycerol and 17.0 ± 1.1% for DMSO + glycerol. We conclude that the function of oocytes was severely affected by both vitrification and exposure to cryoprotectants without vitrification; the best combination of cryoprotectants was EG + DMSO for vitrification of immature buffalo oocytes using either straw or OPS methods.     

Effects of throughfall and litterfall manipulation on concentrations of methylmercury and mercury in forest‐floor percolates

The forest floor was shown to be an effective sink of atmospherically deposited methylmercury (MeHg) but less for total mercury (Hg_total). We studied factors controlling the difference in dynamics of MeHg and Hg_total in the forest floor by doubling the throughfall input and manipulating aboveground litter inputs (litter removal and doubling litter addition) in the snow‐free period in a Norway spruce forest in NE Bavaria, Germany, for 14 weeks. The MeHg concentrations in the forest‐floor percolates were not affected by any of the manipulation and ranged between 0.03 (Oa horizon) and 0.11 (Oi horizon) ng Hg L^–1. The Hg_total concentrations were largest in the Oa horizon (24 ng Hg L^–1) and increased under double litterfall (statistically significant in the Oi horizon). Similarly, concentrations of dissolved organic C (DOC) increased after doubling of litterfall. The concentrations of Hg_total and DOC correlated significantly in forest‐floor percolates from all plots. However, we did not find any effect of DOC on MeHg concentrations. The difference in the coupling of Hg_total and MeHg to DOC might be one reason for the differences in the mobility of Hg species in forest floors with a lower mobility of MeHg not controlled by DOC.     

猴头菌不同菌株降解力与产量关系的研究

对猴头菌3个菌株在菌丝长满袋,第一、二潮菇采收后,基物失重、纤维素和木质素的减少率与产量进行了测定,结果表明:H05菌株对基物降解力最强,子实体转化率也高,8406次之;8413菌株最差。用通径分析表明,基物通过纤维素的降解直接影响子实体产量,随纤维素的含量减少,产量逐步提高,而木质素的降解与菌丝生长速度和生长量关系密切。     

农药混剂的选择毒性研究

稻瘟净或异稻瘟净与乐果或马拉松混用,对抗性黑尾叶蝉有明显的增效作用,对小白鼠急性口服毒性也有所增加。小白鼠口服稻瘟净或异稻瘟净后,鼠肝中水解乐果和N—甲基正己酰胺的羧酰胺酶活力明显下降;水解醋酸α-萘酯的羧酸酯酶活力也被抑制。羊肝微粒体的羧酰胺酶在体外分别被稻瘟净、异稻瘟净、磷酸三苯酯、磷酸三甲苯酯、苯硫磷、氧乐果和西维因强烈抑制,它们的I_(50)值为1.3×10~(-8)—4.0×10~(-5)克分子浓度。稻瘟净、异稻瘟净、磷酸三苯酯和西维因分别是羊肝羧酰胺酶和羧酸酯酶的竞争性抑制剂,它们的K_i值在4.8×10~(-8)—1.0×10~(-7)克分子浓度之间。这些结果表明稻瘟净、异稻瘟净等增加乐果和马拉松对哺乳动物的毒性的机制,可能主要是由于它们抑制了哺乳动物体内正常解毒乐果和马拉松的水解酶。文中讨论了这些农药混剂的选择毒性问题。     

Surface contact toxicity and synergism of several insecticides against different stages of the tropical bed bug, Cimex hemipterus (Hemiptera: Cimicidae)

BACKGROUND: Five formulated insecticides (lambda‐cyhalothrin at 10 mg m^?2, bifenthrin at 50 mg m^?2, fipronil at 10 mg m^?2, fenitrothion at 50 mg m^?2, imidacloprid at 5 mg m^?2) and one active ingredient (DDT at 500 mg m^?2) were evaluated using a surface contact method against early and late instars and adults of two strains of the tropical bed bug, Cimex hemipterus (F.). Synergism of lambda‐cyhalothrin and fipronil using piperonyl butoxide (PBO) was also assessed. RESULTS: The order of susceptibility of different stages of bed bugs was as follows: early stage ? lambda‐cyhalothrin > bifenthrin = imidacloprid > fipronil > fenitrothion > DDT; late stage—lambda‐cyhalothrin > bifenthrin > fenitrothion > imidacloprid > fipronil > DDT; adult—lambda‐cyhalothrin > imidacloprid > bifenthrin > fenitrothion > fipronil > DDT. The late instars exhibited significantly higher LT₅₀ among the life stages. The addition of PBO to fipronil increased the susceptibility of the insects. CONCLUSIONS: Lambda‐cyhalothrin, bifenthrin, fenitrothion and fipronil at the recommended application rates were effective against C. hemipterus. Although imidacloprid demonstrated good initial response against C. hemipterus, the insects showed substantial recovery 72 h post‐treatment. The late instars (fourth and fifth instars) should be used as the model for toxicological evaluation. Copyright © 2011 Society of Chemical Industry     

兽药企业设备维修人员的工作思路

对于集兽用疫苗研发、生产、销售为一体的兽药企业，生产、检验用设备，仪器种类繁多，这就要求有一支与之相适应的维修管理队伍，笔者从事该行业设备维修管理工作十多年，有一些设备维修、改造方面的经历，现就这方面的经历提出几点思路，谨供同行参考。     

Degradation of organotin compounds in organic and mineral forest soils

Broad industrial application of organotin compounds (OTC) leads to their release into the environment. OTC are deposited from the atmosphere into forest ecosystems and may accumulate in soils. Here, we studied the degradation of methyltin and butyltin compounds in a forest floor, a mineral, and a wetland soil with incubation experiments at 20 °C in the dark. OTC degraded slowly in soils with half‐lives estimated from 0.5 to 15 years. The first order degradation rate constants of OTC in soils ranged from 0.05 to 1.54 yr^–1. The degradation rates in soils were generally in the order mono‐ ≥ di‐ > tri‐substituted OTC. Stepwise dealkylation was observed in all cases of di‐substituted OTC, but only in some cases of tri‐substituted OTC. Decomposition rates of OTC in the forest floor were higher than in wetland and mineral soils. Tetramethyltin in the gas phase was not detected, suggesting little tin methylation in the wetland soils. Slow degradation of OTC in soils might lead to long‐term storage of atmospherically deposited OTC in soils.     

Beta-arrestin 2 mediates endocytosis of type III TGF-beta receptor and down-regulation of its signaling

beta-Arrestins bind to activated seven transmembrane-spanning (7TMS) receptors (G protein-coupled receptors) after the receptors are phosphorylated by G protein-coupled receptor kinases (GRKs), thereby regulating their signaling and internalization. Here, we demonstrate an unexpected and analogous role of beta-arrestin 2 (betaarr2) for the single transmembrane-spanning type III transforming growth factor-beta (TGF-beta) receptor (TbetaRIII, also referred to as betaglycan). Binding of betaarr2 to TbetaRIII was also triggered by phosphorylation of the receptor on its cytoplasmic domain (likely at threonine 841). However, such phosphorylation was mediated by the type II TGF-beta receptor (TbetaRII), which is itself a kinase, rather than by a GRK. Association with betaarr2 led to internalization of both receptors and down-regulation of TGF-beta signaling. Thus, the regulatory actions of beta-arrestins are broader than previously appreciated, extending to the TGF-beta receptor family as well.