外源胆固醇对水稻根端线粒体膜流动性的影响

应用荧光探剂 1,6-二苯基-1,3,5-己三烯(DPH)观察外源胆固醇对水稻极端线粒体膜流动性的影响。结果表明,无论外源胆固醇通过水培根系吸收或是直接添加给予水稻根端线粒体,都能使DPH与线粒体结合后的荧光强度减弱,使荧光偏振度和微粘度降低,增加水稻根端线粒体膜流动性。     

抗寒剂对水稻线粒体膜流动性的冷稳定作用

抗寒剂对水稻线粒体膜流动性的冷稳定作用王红,简令成,张举仁（中国科学院植物研究所,北京１０００４４）（山东大学生物系,济南２５０１００）ＥＦＦＥＣＴＯＦＴＨＥＣＯＬＤ－ＲＥＳＩＳＴＥＲＣＲ－ＲＥＳＩＳＴＥＲＣＲ－４ＯＮＴＨＥＣＯＬＤ－ＳＴＡＢＩＬＩＴ...     

烧伤血浆中分子物质对豚鼠心肌线粒体膜流动性的影响

生物膜流动性的改变,可以影响物质转运、能量代谢等许多功能。为了探讨烧伤血浆中分子物质(burned middle molecular substances,BMMS)对心泵功能抑制作用的机理,本研究观察了不同浓度BMMS及正常血浆中分子物质(normal middle molecular substances,NMMS)对正常豚鼠心肌线粒体膜流动性的影响,并与35％体表Ⅲ度烧伤后8h豚鼠心肌线粒体膜流动性的变化相比较。     

外源氯化胆碱可提高小麦线粒体膜的流动性

分别用ANS、DPH及16 -NS三种不同的标记物标记小麦黄化苗的线粒体 ,研究氯化胆碱 (cholinechloride,CC)对线粒体膜的荧光光谱、平均微粘度 (η )及ESR图谱的影响。结果表明 ,0.21 -1.79mmol·L-1 的CC均能显著降低线粒体膜的荧光强度、η 值及ESR图谱的序参数 (S)和旋转相关时间 (τc) ,表明CC可增加线粒体膜的流动性。为揭示CC的提高植物抗冷机制提供依据     

九种常用杀虫剂对二化螟线粒体ATPase活力的抑制作用

研究了二化螟Chilo suppressalis线粒体Na⁺-K⁺-ATPase和Ca^2＋-Mg^2＋-ATPase的生物化学性质以及9种常用杀虫剂对这两种酶活性的影响。结果表明, 二化螟线粒体Na⁺-K⁺-ATPase和Ca^2＋-Mg^2＋-ATPase的最适反应条件为pH值7.4,温度37℃。 Na⁺-K⁺-ATPase的米氏常数（Km）为0.42 mmol/L,最大反应速度（Vmax）为302.47 nmol/(min·mg) 。Ca^2＋-Mg^2＋-ATPase的Km为0.40 mmol/L,Vmax为128.04 nmol/(min·mg)。药剂浓度为1×10^-4 mol/L时,5种菊酯类杀虫剂对离体ATPase活性抑制的顺序为：溴氰菊酯>联苯菊酯>百树菊酯>三氟氯氰菊酯和氟硅菊酯;对二化螟Na⁺-K⁺-ATPase的抑制率分别为40.12％、39.69％、27.27％、19.49％和18.71％;对Ca^2＋-Mg^2＋-ATPase的抑制率分别为29.27％、23.78％、19.88％、11.64%和14.34％。硫丹对二化螟Na⁺-K⁺-ATPase和Ca^2＋-Mg^2＋-ATPase的抑制率均为17.46％。甲胺磷和呋喃丹对Ca^2＋-Mg^2＋-ATPase的抑制率分别为27.16％和17.42％,对Na⁺-K⁺-ATPase则几乎没有抑制作用。实验结果还表明, 在1.6×10^-7～1×10^-4 mol/L的浓度范围内,上述9种杀虫剂对二化螟ATPase活性的抑制率存在明显的剂量-效应关系。     

水分胁迫对甘蔗叶片线粒体膜流动性的影响及其与膜脂过氧化的关系

用荧光探剂ANS对抗旱性不同的甘蔗品种在水分胁迫下叶片线粒体膜流动性的变化进行的研究表明,水分胁迫降低了线粒体膜的流动性,抗旱性强的甘蔗品种Co 617和F.Y.79-9的下降幅度分别小于抗旱性弱的Co 740和M.T.77-208;水分胁迫下线粒体膜流动性的下降与膜脂过氧化产物丙二醛含量的增加有密切关系。外源自由基处理试验也表明,甘蔗叶片线粒体膜流动性的下降与膜脂过氧化作用有关。     

鲢,鲮线粒体膜DPH荧光偏振研究

鲢(Hypophthalmichthys molitrix)、鲮(Cirrhina molitorella)肝线粒体膜的DPH荧光偏振度均随温度的升高而降低,即膜的流动性随温度升高而增大,且在36—38℃之间存在相变。但在鲢鱼线粒体膜同时还具有一个“动力学折点”,在鲮鱼不具有这一特性。结果分析表明,鲢、鲮线粒体膜的这种差异可能与其温度适应的调节机制有关。     

荧光偏振法测定肺细胞线粒体膜的流动性

本文在线粒体膜能量偶联ATP酶与矽肺发病关系研究的基础上进一步作矽尘对肺细胞线粒体膜流动性的影响。 材料和方法 1.动物 纯系Wistar雄性大白鼠体重250g左右,每个剂量组40只,按10 mg/ml、30 mg/ml和50mg/ml三种不同剂量的石英粉尘一次气管注入,染尘     

Effects of Hexaflumuron and Pyriproxyfen on the purified Phenoloxidase of Chilo suppressalis Walker (Lepidoptera: Crambidae)

Effects of two insect growth regulators (IGRs), hexaflumuron and pyriproxyfen, were studied on the purified phenoloxidase (PO) of Chilo suppressalis. Purification procedure revealed two isozymes of PO, namely POI and POII. IC₅₀ concentrations of hexaflumuron and pyriproxyfen on POI were 0.36, 0.23?μg/ml and on POII were 0.105, 0.42?μg/ml, respectively. Determination of optimal pH and temperature revealed pH 5 and temperature 40?°C as the optimal values for the enzymatic activity. Treating POs with IC₅₀ concentrations of two IGRs was pH and temperature dependent. Effects of these IGRs on POI caused significant increase of K_m value versus control suggesting competitive inhibition. Hexaflumuron and pyriproxyfen cause reduction in V_max value of POII versus control suggesting non-competitive inhibition. The current study shows direct effects of two IGRs on purified PO of C. suppressalis for the first time. These findings could be helpful to develop safe compounds with inhibitory mechanism on PO to neutralise insect immune responses against entomopathogenic agents.     

Alterations in erythrocyte membrane fluidity in children with trisomy 21: a fluorescence study.

Membrane fluidity of erythrocytes obtained from 15 children with trisomy 21 and 20 healthy controls were studied by measuring steady-state fluorescence anisotropy and fluorescence lifetime of 1,6-diphenyl-1,3,5-hexatriene (DPH) and 1-(4-trimethylammoniumphenyl)-6-phenyl-1,3,5-hexatriene (TMA-DPH) incorporated in hemoglobin-free erythrocyte membranes. Our results demonstrate a significant decrease in DPH fluorescence anisotropy and a significant increase in TMA-DPH fluorescence anistropy in erythrocytes from subjects with trisomy 21. No significant differences between the two groups were observed in the fluorescence lifetime of DPH and TMA-DPH. These data suggest an increase in membrane fluidity in the interior part of the membrane and a decrease in fluidity at the lipid-water interface region. This could be in part attributed to an increased oxidative damage in trisomy 21.     

温度胁迫对二化螟滞育幼虫生理指标的影响

为从生理生化水平上探讨二化螟滞育幼虫应对温度胁迫的生理机制,分别对系列温度胁迫(STS)和梯度温度胁迫(GTS)处理后的幼虫水、脂质、总糖、小分子碳水化合物含量及超氧化物歧化酶(SOD)、过氧化物酶(POD)、过氧化氢酶(CAT)活性进行了测定.结果表明:随着温度的降低,两种处理二化螟滞育幼虫虫体含水量趋于减少,且0℃以下时GTS处理下降幅度较STS处理显著;两种处理脂质含量均逐步下降且二者间无显著差异;两种处理总糖含量分别先减后增和持续下降,均检测出4种小分子碳水化合物,其中STS处理葡萄糖、甘油和果糖含量先增后减,海藻糖含量变化与此相反,而GTS处理海藻糖含量先减后增,葡萄糖和甘油含量呈相反变化,果糖含量无变化;14～-14℃范围内STS处理SOD和POD活性较GTS处理低,CAT活性相反.二化螟滞育幼虫生理指标的变化反映了其应对不同温度胁迫的生理响应.     

Effects of alcohols on ADP-induced aggregation and membrane fluidity of gel-filtered bovine blood platelets

Summary The effects of four alcohols—n-propyl,n-butyl,n-amyl andn-hexyl alcohol—on the ADP-induced aggregation of gel-filtered bovine platelets were examined. All four alcohols inhibited the aggregation, the order of their effects beingn-propyln-amyl<n-hexyl. Comparison of the inhibitory effects of the alcohols with their physico-chemical properties showed that their degrees of inhibition depended on their hydrophobicities. Moreover, it was suggested that their interaction with the lipid layer of the membrane was important for the inhibition. Studies on the effects of alcohols on the fluorescence polarization of 1,6-diphenyl-1,3,5-hexatriene-labeled platelets showed that the membrane fluidity of the platelets increased in the same concentration range in which aggregation inhibition was observed. Since the alcohols inhibited aggregation without affecting Ca²⁺ mobilization in the platelets, as revealed in this study, it was concluded that inhibition of platelet aggregation was due to perturbation of membrane lipids by the alcohols. This hypothesis is supported by several recent studies on the effects of cholesterol and cations, which suggest that a relatively rigid membrane favors platelet aggregation.     

Effects of delayed mating and male mating history on longevity and reproductive performance of the rice stem borer, Chilo suppressalis (Walker) (Lep., Pyralidae)

Abstract:  The mating potential, effects of delayed mating and male mating history on longevity and reproductive performance of female rice stem borer (RSB), Chilo suppressalis , were investigated under laboratory conditions. Given the opportunity, RSB males copulated an average of 2.7 times, while females generally mated only once. Females were more severely affected by mating delay than males in terms of female longevity and reproductive performance. With increasing age at mating, females' longevity increased, while oviposition period, fecundity and egg fertility decreased. Mean fecundity and egg fertility of females mated 1 and 7 days after emergence were 251.3% and 99.2%, and 96.2% and 75.5% respectively. Both were reduced significantly when female mating was delayed beyond 4 days after emergence. However, irrespective of the first mating age and different mating history of the males, the results indicated that both did not result in a significant difference in the quality of their contributions to female longevity and reproductive performance. The results obtained in this study are discussed in relation to the potential effect on pheromone control of RSB.     

Influence of increased membrane cholesterol on membrane fluidity and cell function in human red blood cells

Cholesterol and phospholipid are the two major lipids of the red cell membrane. Cholesterol is insoluble in water but is solubilized by phospholipids both in membranes and in plasma lipoproteins. Morever, cholesterol exchanges between membranes and lipoproteins. An equilibrium partition is established based on the amount of cholesterol relative to phospholipid (C/PL) in these two compartments. Increases in the C/PL of red cell membranes have been studied under three conditions: First, spontaneous increases in vivo have been observed in the spur red cells of patients with severe liver disease; second, similar red cell changes in vivo have been induced by the administration of cholesterol-enriched diets to rodents and dogs; third, increases in membrane cholesterol have been induced in vitro by enriching the C/PL of the lipoprotein environment with cholesterol-phospholipid dispersions (liposomes) having a C/PL of >1.0. In each case, there is a close relationship between the C/PL of the plasma environment and the C/PL of the red cell membrane. In vivo, the C/PL mole ratio of red cell membranes ranges from a normal value of 0.9–1.0 to values which approach but do not reach 2.0. In vitro, this ratio approaches 3.0. Cholesterol enrichment of red cell membranes directly influences membrane lipid fluidity, as assessed by the rotational diffusion of hydrophobic fluorescent probes such as diphenyl hexatriene (DPH). A close correlation exists between increases in red cell membrane C/PL and decreases in membrane fluidity over the range of membrane C/PL from 1.0 to 2.0; however, little further change in fluidity occurs when membrane C/PL is increased to 2.0–3.0. Cholesterol enrichment of red cell membranes is associated with the transformation of cell contour to one which is redundant and folded, and this is associated with a decrease in red cell filterability in vitro. Circulation in vivo in the presence of the slpeen further modifies cell shape to a spiny, irregular (spur) form, and the survival of cholesterol-rich red cells is decreased in the presence of the spleen. Although active Na-K transport is not influenced by cholesterol enrichment of human red cells, several carrier-mediated transport pathways are inhibited. We have demonstrated this effect for the cotransport of Na + K and similar results have been obtained by others in studies of organic acid transport and the transport of small neutral molecules such as erythritol and glycerol. Thus, red cell membrane C/PL is sensitive to the C/PL of the plasma environment. Increasing membrane C/PL causes a decrease in membrane fluidity, and these changes are associated with a reduction in membrane permeability, a distortion of cell contour and filterability and a shortening of the survival of redcells in vivo.     

Effects of membrane lipid and fluidity modifications on HIV-1 infectibility of primate lymphocytesin vitro

Although most non-human primates, except the chimpanzee and the gibbonin vivo are not infectible by HIV-1, lymphocytes of several of these species can be infected by HIV-1in vitro.In order to investigate whether thein vitro infectibility of primate lymphocytes might be attributed to plasma membrane adaptation processes or to serum factors, we compared HIV-1 infectibility of cultivated peripheral blood lymphocytes of macaques and of baboons on day one and on day ten of cultivation. These data were correlated to plasma membrane lipid composition and membrane fluidity.We found a correlation between increased HIV-1in vitro infectibility and changes in plasma membrane lipid composition resulting in decreased membrane fluidity of cultured primate lymphocytes.     

Role of lindane in membranes. Effects on membrane fluidity and activity of membrane-bound proteins

The influence of lindane (gamma-hexachlorocyclohexane) on fluidity of plasma membranes from rat renal cortical tubules has been investigated. Preincubation with lindane increased membrane fluidity. This effect was accompanied by (i) a decrease in the transport of glucose with regard to the controls and (ii) an inhibition of the -adrenergic stimulatory activity upon cyclic AMP accumulation. However, a significant decrease of the membrane fluidity was found when rats were injected with lindane for 12 days. The injection of lindane exerted the opposite effect on the membrane proteins, the glucose transporter and the -adrenergic receptor, enhancing the glucose uptake and increasing the isoproterenol-stimulated cycle AMP accumulation. A possible explanation of the difference could involve a resistance to membrane disordering by lindane through a regulatory mechanism that would balance the activity of many lindane-sensitive proteins in insecticide-injected rats.     

Effects of dibromothymoquinone on mung bean mitochondrial electron transfer and membrane fluidity

The effects of the quinone analog dibromothymoquinone on electron transfer in isolated mung bean mitochondria are described. Both the main, cyanidesensitive and the alternate, cyanide-insensitive pathways are inhibited by dibromothymoquinone but in markedly different fashions. Half-maximal inhibition appeared at 40 μM and 20 μM dibromothymoquinone for the cyanide-sensitive and alternate pathways, respectively. With succinate as the electron donor, dibromothymoquinone inhibited the alternate pathway at a single site; showing a mixed, non-competitive type inhibition. On the succinate, cyanide-sensitive pathway dibromothymoquinone showed two sites of inhibition and neither coincides with the site of inhibition associated with the alternate pathway. With malate as the electron donor, two sites of inhibition by dibromothymoquinone were observed regardless of the pathway measured.Dibromothymoquinone also inhibited the rate of valinomycin-induced swelling of isolated mung bean mitochondria. Steady-state kinetics showed the inhibition to be non-competitive with respect to valinomycin. Additionally dibromothymoquinone was observed to increase the fluorescence polarization associated with the hydrophobic probe 1,6-diphenylhexatriene. The results indicated that dibromothymoquinone decreased the fluidity of the inner mitochondrial membrane and suggested that the inhibition of mitochondrial electron transfer by dibromothymoquinone may be associated with this decrease in membrane fluidity.The relationship of the multisite nature of the inhibition of electron transfer by dibromothymoquinone and the possible role of mobile electron carriers such as ubiquinone on the main and alternate respiratory pathways of higher plants is discussed.     

Reduced lateral mobility of a fluorescent lipid probe in cholesterol-depleted erythrocyte membrane

The effect of cholesterol depletion of the human erythrocyte membrane on the lateral diffusion rate of a fluorescent lipid probe is reported. At low temperatures (?5 to 5°C), the diffusion of the probe is 50% slower in the cholesterol-depleted membrane than in non-depleted membrane. At high temperatures (30 to 40° C), probe mobility is not affected by cholesterol depletion. These results suggest that cholesterol suppresses aspects of phospholipid phase changes in animal cells in a manner consistent with its behavior in artificial bilayers and multilayers.Whole erythrocytes were depleted of 30–50% of their cholesterol by incubation with a sonicated dispersion of dipalmitoyl phosphatidylcholine. Cells were then labeled with 3,3′-dioctadecylindocarbocyanine (diI), a phospholipid-like fluorescent dye, and hemolyzed into spherical ghosts. The rate of lateral motion of diI was measured by observing the fluorescence recovery after local photobleaching with a focused laser spot.The diffusion rate of the lipid probe in both control and cholesterol-depleted erythrocyte membrane is substantially smaller than in any cell or model membrane previously measured.