干旱胁迫对不同种源云南松幼苗生物量与根系形态的影响

通过盆栽控水，采用双因素随机区组设计研究了9个不同地理种源云南松幼苗生物量分配和根系形态对干旱胁迫的响应，比较了干旱胁迫下幼苗生物量及其分配以及根系形态在种源间的差异，并通过隶属函数法对不同种源幼苗干旱适应性进行了初步评价。结果表明:1）干旱胁迫下，各种源云南松幼苗地径下降明显，苗高未发生显著变化，各器官生物量和总生物量多呈下降趋势，干旱胁迫并没有导致幼苗根生物量分配比和根冠比的增加，但根系长、比根长、根表面积和比根面积在干旱胁迫下增加显著。2）不同种源云南松幼苗地径、苗高、生物量及其分配比和根系形态在干旱处理下均存在显著差异，其中地径和苗高分别以西昌和双柏种源最大，各器官生物量和总生物量以双柏、西昌和册亨种源较高，察隅种源各器官和总生物量较低，但该种源具有最大的根生物量分配比和根冠比；会泽种源根长、根表面积、比根长和比根面积均最大。研究发现，在土壤水分限制条件下，云南松幼苗以根系形态变化代替根系生物量增加的策略来适应干旱，各种源云南松幼苗生长对干旱胁迫响应的差异可能是由种源地理气候因子长期影响所形成的不同适应性策略所导致。经平均隶属函数值法初步评价了不同种源云南松幼苗对干旱适应性的强弱，结果显示，西藏察隅、云南会泽和四川西昌种源对土壤干旱的适应性较强，云南双柏、贵州册亨、云南云龙种源居中，而云南新平、永仁和禄丰种源适应性较弱。     

下丘脑-垂体-肾上腺轴参与动物采食调控的研究进展

采食是动物维持生命活动的基本生理过程，是动物生长发育的基础。畜禽采食量的高低直接影响到营养物质的摄入量及生产性能的发挥。在畜牧业生产中，影响采食的因素很多，而应激是其中一个非常重要的影响因素。动物机体的应激反应主要由下丘脑-垂体-肾上腺（HPA）轴来调控。下丘脑、垂体和肾上腺皮质通过释放促肾上腺皮质激素释放激素（CRH）、促肾上腺皮质激素（ACTH）和糖皮质激素（GC）这3种应激激素来协同调控动物的应激反应。应激激素对采食行为的调节是一个非常复杂的过程，主要通过稳态和非稳态途径来调节采食，可以双向调控食物的摄入量。稳态途径指的是通过调控机体能量稳态而调控采食。CRH和ACTH通过抑制下丘脑促食欲肽的表达而抑制采食；而GC在中枢和外周发挥着完全相反的作用。非稳态途径指的是通过影响中脑奖赏系统调控采食的愉悦感，是近年来食欲调控研究的热点，越来越多的研究证明了应激激素与奖赏系统的联系。作者针对应激激素调控采食的最新研究报道进行综述，以期为生产实践中新型的采食调控技术研发提供一定的参考。     

Effect of endothelin-1 on inflammation and oxidative stress in COPD

AIM:To investigate the effect of endothelin-1 on inflammation and oxidative stress in chronic obstructive pulmonary disease (COPD). METHODS:Healthy non-smokers (30 cases), healthy smokers (30 cases) and COPD patients (29 cases) were collected and induced to produce sputum. The concentration of endothelin-1 in the induced sputum was detected. The model of emphysema was established by cigarette smoke extract to stimulate SD rats. Endothelin A receptor antagonist BQ123 and non-selective endothelin receptor antagonist bosentan were used to intervene with the model rats. The experiment was divided into control group, cigarette-treated group, selective antagonist group and non-selective antagonist group. The protein levels of cleaved caspase-3 in the lung tissue were determined by Western blot. Gelatin zymography was used to analyze the activity of matrix metalloproteinase-2 (MMP-2) and MMP-9 in the lung tissue. The levels of interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were measured by ELISA. The bioantioxidant power (BAP) was detected by BAP assay kit. RESULTS:The concentrations of endothelin-1 in induced sputum of healthy smokers and COPD patients were significantly higher than that of healthy non-smokers (P<0.05), and the level of endothelin-1 in COPD patients was significantly higher than that in healthy smokers (P<0.05). The levels of cleaved caspase-3, MMP-2, MMP-9, TNF-α and IL-1β in the lung tissues from cigarette-treated group were significantly higher than those in control group (P<0.05). The endothelin A receptor antagonist significantly inhibited the levels of cleaved caspase-3, MMP-2, MMP-9, TNF-α and IL-1β (P<0.05). The serum BAP in cigarette-treated group was significantly lower than that in control group (P<0.05). However, endothelin A receptor antagonist significantly increased serum BAP (P<0.05). CONCLUSION:Endothelin-1 may play an important role in the development and progression of COPD through regulating apoptosis, matrix metalloproteinase activity, inflammation and oxidative stress.     

镉胁迫对烟草种子萌发和烟苗生长发育的影响

为探讨不同镉（Cd）胁迫对不同烟草品种种子萌发、幼苗生长的生理生态效应的影响,以吉烟9号、吉烟10号、延晒六号3个烟草品种为材料,研究了不同浓度的Cd溶液对烟草种子萌发以及烟苗生长发育的影响。结果表明,Cd胁迫下烟草种子发芽势、发芽率、发芽指数、活力指数、苗高均受到抑制;烟苗叶绿素含量降低,根冠比变小,生长受到抑制,CAT活性、SOD活性、可溶性糖含量随Cd浓度的增加呈先增后降的趋势,POD活性、MDA含量、Pro含量、Cd含量均随Cd浓度的增加而增加。可见Cd胁迫能不同程度地影响烟草种子萌发和烟苗生长发育,烟苗体内的抗氧化酶系统被破坏,多种酶活性不协调,生理生化过程紊乱,最终导致烟苗受害。     

外源NO及反向调控PEG胁迫下苜蓿萌发种子抗氧化酶及其同工酶动态的研究

以紫花苜蓿为材料,用一氧化氮供体硝普钠(SNP)及一氧化氮清除剂c-PTIO对苜蓿种子进行浸种处理,采用分光光度法和同工酶电泳技术来研究外源NO及反向调控对PEG胁迫下紫花苜蓿抗氧化酶活性及其同工酶的影响,并探讨NO调控苜蓿种子耐旱性的生理机制。结果表明:PEG胁迫下外施0.1 mmol·L^-1 SNP,第6天时较PEG处理POD活性降低了32.72%;第4天时SOD、CAT活性较PEG处理升高了10.48%、23.60%,有效缓解了PEG对紫花苜蓿萌发中种子的氧化损伤,提高其抗氧化能力。PEG胁迫下添加 c-PTIO抑制了苜蓿萌发期的抗氧化系统活性。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随PEG胁迫时间的延长而增加,在第2天酶带只有1条,而第4天酶带呈现9条;SOD和CAT同工酶表达量变化不显著,但酶带强弱有一定变化,S3酶带随处理时间的延长表达量逐渐减弱;CAT同工酶谱带则一直保持2条带,无明显强弱变化。因此,外源NO在PEG胁迫下紫花苜蓿萌发中抗氧化酶快速响应并在维护氧自由基代谢平衡中起重要保护作用。     

Captopril exerts myocardial protective effect in coronary microembolization rats by inhibiting oxidative stress injury and alleviating inflammatory response

AIM: To investigate the effects of captopril (CAP) on oxidative stress injury and inflammatory response induced by coronary microembolization (CME) and its related molecular mechanisms. METHODS: The rat model of CME was established by clamping the rat artery and injecting blood microemboli. The rats were divided into control group, CME group and CME+CAP group, with 6 rats in each group. The myocardial tissues of each group were collected. The changes of myocardial structure and the degree of inflammatory response were analyzed by HE staining. Cardiomyocyte apoptosis was detected by TUNEL staining. The fluorescence intensity of cleaved caspase-3 was detected by immunofluorescence obervation. The protein levels of cleaved caspase-3 and Bax were determined by Western blot. The activity of superoxide dismutase (SOD) and catalase was measured by ELISA. The production of reactive oxygen species (ROS) was detected by DHE fluorescence staining. RESULTS: CAP significantly reduced the myocardial structural changes (P<0.05), inflammatory cell infiltration (P<0.01), number of apoptotic cardiomyocytes (P<0.01), the protein levels of cleaved caspase-3 and Bax (P<0.01), and ROS production levels (P<0.01), but promoted the activity of antioxidant markers SOD and catalase (P<0.01) in the CME rats.CONCLUSION: CAP attenuates CME-induced myocardial injury by resisting oxidative stress and alleviating inflammatory response.     

Expression and functional characterization of glutamine synthetase from giant freshwater prawn (Macrobrachium rosenbergii) under osmotic stress

The freshwater prawn, Macrobrachium rosenbergii naturally lives in the freshwater, though it migrates to the brackish water environment during spawning that claimed to be resistant on a broad range of saline fluxes. However, little is known about the osmoregulatory patterns and the effect of an enzyme glutamine synthetase (GS) in M. rosenbergii under stress. Here, we described the identification and functional characterization of GS from M. rosenbergii (Mr‐GS) at molecular and protein levels. The identified Mr‐GS was comprised of 361 amino acids that phylogenetically shared the highest identity with other crustaceans and predicted to contain Gln‐synt_C and Gln‐synt_N domains at the respective terminal regions. Tissue distribution analysis in M. rosenbergii revealed that the Mr‐GS was highly expressed in muscle, and commonly existed in other examined tissues in the following order gills > heart > stomach > brain > haemolymph. Whereas, the mRNA of Mr‐GS was significantly up‐regulated in the muscle and gill tissues following challenges with either hyper (0 → 13‰), or hypo (13 → 0‰) osmotic stress at 3, 6 and 12 hr. Furthermore, the level of Glutamine concentration was positively correlated with the GS mRNA and protein expression patterns in hyper‐osmotic stress, whereas in hypo‐osmotic stress a slight decrease in the gills and maintained a level in the muscle tissues at 3, 6 and 12 hr post‐treatments. Our findings suggest that Mr‐GS potentially exhibited the osmoregulation responses in the gill and muscle tissues of M. rosenbergii throughout the time of osmotic stress, which will benefit for future study on osmoregulation.     

Trx-1 over-expression attenuates oxidative stress injury in MPP+ -induced PC12 cells by regulating NF-κB signaling pathway

AIM:To investigate the inhibitory effect of thioredoxin 1 (Trx-1) over-expression on oxidative stress injury in 1-methyl-4-phenylpyridinium (MPP⁺)-induced rat pheochromocytoma PC12 cells by regulating NF-κB signaling pathway.METHODS:The PC12 cells were damaged by treatment with MPP⁺ at 1, 3 and 5 mmol/L, and the optimal concentration of 3 mmol/L was selected. The cell viability was measured by MTT assay. The oxidative stress indexes lactate dehydrogenase (LDH) activity, superoxide dismutase (SOD) activity and malondialdehyde (MDA) content in the cell culture supernatant were detected, and the protein expression of Trx-1 was determined by Western blot. Lentiviral infection with Ad-Trx-1-GFP sequence was used to establish a model of MPP⁺-treated PC12 cells with Trx-1 over-expression. The effects of Trx-1 over-expression on the cell viability, oxidative stress responses and NF-κB signaling pathway were determined by MTT assay, commercial kits and Western blot. The effects of phorbol 12-myristate 13-acetate (PMA), an activator of NF-κB signaling pathway, on the viability and oxidative stress of PC12 cells were observed. The NF-κB signaling pathway inhibitor pyrrolidine dithiocarbamate (PDTC) was used in MPP⁺-treated PC12 cells with Trx-1 over-expression, and the cell viability and oxidative stress responses were measured. RESULTS:The viability of PC12 cells, SOD activity in the supernatant and protein expression of Trx-1 were decreased, while LDH activity and MDA content in the supernatant were increased significantly by treatment with MPP⁺ at 1, 3 and 5 mmol/L. The effect of MPP⁺ at 3 mmol/L and 5 mmol/L was significantly greater than that at 1 mmol/L (P<0.05), and no significant difference between 3 mmol/L and 5 mmol/L was observed (P>0.05). The inhibitory effect of MPP⁺ on the viability of PC12 cells, and the oxidative stress injury and activation of NF-κB signaling pathway induced by MPP⁺ were significantly attenuated by over-expression of Trx-1. The inhibitory effect of MPP⁺ on the viability of PC12 cells and the oxidative stress injury induced by MPP⁺ were promoted by the activation of NF-κB signaling pathway, while the protective effects of Trx-1 over-expression on the MPP⁺-treated PC12 cells were enhanced by the inhibition of NF-κB signaling pathway. CONCLUSION:Over-expression of Trx-1 protects MPP⁺-treated PC12 cells from oxidative stress injury by regulating NF-κB signaling pathway.