红枣提取物对虹鳟血清指标和头肾免疫相关基因表达的影响

为了探讨添加红枣提取物对促进虹鳟(Oncorhynchus mykiss)机体健康的可能性,选取体长为7.2~8.4 cm的健康虹鳟,随机分成4个试验组,分别投喂红枣提取物添加量为0%(对照组)、0.25%、0.50%和1.00%的等氮等脂饲料,饲养56 d,养殖结束后测定12项血清生化指标和头肾的6个免疫相关基因mRNA表达量。结果显示:与对照组相比较,血清中肌酐(CREA)和尿素氮(BUN)含量三个红枣提取物组均出现极显著下降;谷丙转氨酶(GPT)活性在0.50%和1.00%组极显著下降,谷草转氨酶(GOT)活性也在0.50%和1.00%组出现了一定程度下降,但差异不显著;酸性磷酸酶(ACP)和碱性磷酸酶(AKP)活性无显著变化;总蛋白(TP)和白介素6(IL-6)含量在0.25%组出现显著增加;溶菌酶(LZM)活性三个红枣提取物组均显著升高;超氧化物歧化酶(SOD)活性在0.50%组极显著增加;补体4(C4)和肿瘤坏死因子(TNF-α)含量在0.25%和0.50%组均极显著增加。在头肾中,与对照组相比,SOD、白介素1β(IL-1β)和补体3(C3)基因表达量在0.50%和1.00%组均为显著或极显著上调;Factor H基因表达量在0.50%组显著上调;过氧化氢酶(CAT)和LZM基因表达量在0.50%和1.00%组仅出现差异不显著上调。上述结果表明,在虹鳟饲料中添加一定量的红枣提取物,可以起到促进肾功能,保护肝脏和提高其非特异性免疫功能的作用。     

牛奶葡萄贮藏中SO_2伤害及调控措施研究

牛奶葡萄采后SO2双重释放装置辅以CT－1处理不但有效降低了药害发生率，而且提高了贮藏效果。在此基础上辅以采前喷布内含杀菌剂的壳多糖，牛奶葡萄可达到更佳贮藏效果，在1998年生长季发生全国性洪水灾害，田间带菌量剧增，各地葡萄贮藏效果极差情况下，参试的牛奶葡萄腐烂率只有1．6％，果梗鲜绿，褐变指数只有0．4％，药害率仅为1．0％，果肉亚硫酸盐残留仅为0．067 mg／kg。     

紫花苜蓿受冻害后促进根颈枝条再生方法的研究

对蔚县苜蓿根颈冻害后切除冻伤部分处理的比较研究结果表明,处理区的根颈苗数、地上高度、地上生物量、分蘖丛数是对照区的1.6～2倍;处理区苜蓿的各个数量指标的b值大于对照处理苜蓿b值,说明除冻害根颈后苜蓿的生长比不除冻害根颈部分的苜蓿生长更为合理。通过除去苜蓿冻害部位,防止根系继续腐烂,保护了未冻害部分,增加了苜蓿发芽的有效部位。同时,使根系与地面的距离变短或露出地面,增加光照强度,提高地温,促使未冻害苜蓿根系发芽,返青提前增加产量。     

Postanesthetic Pulmonary Edema In an Arab Stallion

A six-year-old arabian stallion was admitted to The Ohio State University Veterinary Hospital for evaluation and repair of a comminuted fracture of the second phalanx. The horse developed impaired arterial oxygenation during surgey and pulmonary edema post-operatively. We postulate that impaired arterial oxygenation resulted from atelectasis of the dependent lung during annesthesia, and the pulmonary edema occurred following re-expansion of the atelectatic of the initiating cause of the edema, removal of excess lung water from the alveoli, and restoration of normal arterial oxygenation. The horse was fully recovered within 12 hours of initiation of clinical signs of respiratory compromise. The horse was fully recovered within 12 hours of initiation of clinical signs of respiratory compromise. This report describes re-expansion pulmonary edema due to reperfusion injury in a horse, treatment of the condition, and a possible explanation of the pathogenesis of this pulmonary pathology.     

Feline Ubiquitin Fusion Protein Genes

Using cDNA from a CRFK cell line as a template, PCR amplification was performed with the Ub1S and poly(dT) primers to isolate feline ubiquitin genes. Sequencing of the 495 bp PCR fragment revealed that the putative amino acids induced by this fragment gave a fusion protein consisting of a ubiquitin polypeptide (76 amino acids) and an extension protein of ribosomal proteins L40 (52 amino acids). The putative amino acid sequence of ubiquitin was identical to those of humans, rats and pigs.The recombinant glutathione S-transferase (GST)–feline ubiquitin fusion proteins were produced in Escherichia coli and purified. The fusion proteins had a molecular weight of about 42 kDa and were detected by immunoblot assay with rabbit anti-ubiquitin antiserum.The mRNAs from heat-shocked and non-heat-shocked cells were subjected to RT-PCR (Ub1S and poly(dT) primers) analysis. The molecular weights of the ubiquitinated proteins in heat-shocked CFRK cells were between 18 kDa and 24 kDa by immunoblot assay.These results suggested that there were more ubiquinated proteins in the heat-shocked CRFK cells than in the pre-heat-shocked cells.     

低氧适应动物喜马拉雅旱獭的组织学观察

对生活在青藏高原（海拔３２００－３４００m）喜马拉雅旱獭的肝脏、肺、肾、卵巢、甲状腺等器官结构进行了组织学观察。     

橡胶树低温伤害的生理反应

在人工零上低温下,巴西橡胶树(Hevea brasiliensis)叶质膜透性随低温处理时间的延长而持续上升,抗冷品系的上升速率比不抗冷品系慢。呼吸强度和ATP含量均随处理时间的延长而持续下降,抗冷品系下降速率比不抗冷品系慢。叶绿体Mg~(++)—ATPase活性也表现出明显抗性差异。可见,低温下叶组织的质膜透性、呼吸强度、ATP含量以及Mg~(++)—ATPase活性的变化与品系抗冷性有关。低温下呼吸强度、ATP含量与质膜透性变化呈负相关,质膜透性的变化与供能有关。     

Influence of ischemia-reperfusion on apoptosis of sinoatrial node cells in rabbits in vivo

AIM:To study influence of ischemia-reperfusion(IR) on apoptosis and expression of apoptosis-related genes Fas-L, Bax and Bcl-2 of sinoatrial node(SAN) cells in rabbits in vivo. METHODS:Ninety healthy adult rabbits were divided randomly into control group, ischemia groups (I_{10 min}, I_{30 min}, I_{60 min} and I_{120 min}) and IR groups (I_{10 min}R_4h, I_{30 min}R_4h, I_{60 min}R_4hand I_{120 min}R_4h). IR injury model of SAN was established by occluding and loosening the start section of right coronary artery. The apoptosis of SAN cells was detected by TUNEL staining. The expression of Fas-L, Bax and Bcl-2 of SAN cells was detected by immunohistochemistry. RESULTS:①No obvious apoptosis of SAN cells was observed in control group, I_{10 min} and I_{30 min} groups. Apoptosis of different degrees in SAN cells were found in 68.3%(41/60) rabbits in I_{60 min}, I_{120 min} and 4 subgroups of IR. ②The highest expression of Fas-L and Bax was observed in I_{120 min} group and that of Bcl-2 was in I_{60 min} group. ③The highest expression of Fas-L and Bax was observed in I_{60 min}R_4h group. The peak level of Bcl-2 was observed in I_{30 min}R_4h group. ④The expression of Fas-L and Bax was significant higher in IR group than that in ischemic group at the same time point. CONCLUSION:Ischemia and IR induced apoptosis of SAN cells in rabbit in vivo. Fas-L、Bax、Bcl-2 may participate in the regulation of apoptosis and the injury during IR aggravates the apoptosis of SAN cells.     

Effect of protein kinase C on the expression of myocardial HSP70 mRNA during myocardic ischemic preconditioning in rabbits

AIM:To study the relationship between myocardial HSP70 and PKC during myocardial ischemic preconditioning(IPC). METHODS: PKC inhibitor, polymyxin B(PMB) and PKC activator, phorbol 12-myristate 13-acetate(PMA) were applied to the models of myocardial ischemia/reperfusion in vivo and in vitro in rabbits, respectively, and the ventricular functions, PLA₂ in the serum, and the expression of mycardial HSP70 mRNA were examined. RESULTS:IPC decreased PLA₂ activity, improved the left ventricular function and increased the expression of myocardial HSP70 mRNA. Howerer, all these effects of IPC could be blocked by PMB. Interestingly, PMA mimicked IPC with attenuating the injuries of cardial myocytes and increasing myocardial HSP70 mRNA expression. CONCLUSION:PKC is involved in the myocardial HSP70 expression in case of ischemic preconditioning.