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91.
代解杰 《中国实验动物学报》2005,(Z1)
[目的]评价抗黄体酮(mifepristone)联合Aromatase抑制剂(letrozole或aminoglutethimide)或iNOS抑制剂(aminoguandine)是否能有效终止恒河猴早期妊娠。[方法]将30只猴子随机分为5组(治疗组每组6只,对照组6只),并在妊娠30,31和32天进行如下处理:对照组,每只动物1ml安慰剂;A组,Mifepristone(1mg/kg,sc.);B组,Mifepristone(sc.)+Letrozole(2.5mg/只sc.);C组,Mifepristone(1mg/kg,sc.)+aminoglute-chimide(50mg/kgsc.,bid);D组,Mifepristone(1mg/kg,sc.)+aminoguanidine(150mg/kg,sc.,bid)。所有妊娠猴在妊娠29天通过超声波确认。[结果]在B、C、D组,所有的动物的妊娠都在妊娠早期被终止(6/6)。A组和对照组的妊娠终止率分别为3/6和2/6。同时,联合用药能够有效排空子宫腔和减少出血。[结论]该处理能有效地终止恒河猴早期妊娠。联合用药比用于女人的妊娠治疗更有效,并减少了流血时间,或许可以代替目前的终止妊娠的医疗方法。 相似文献
92.
93.
Chu GH Gu M Cassel JA Belanger S Graczyk TM DeHaven RN Conway-James N Koblish M Little PJ DeHaven-Hudkins DL Dolle RE 《Bioorganic & medicinal chemistry letters》2005,15(23):5114-5119
Two novel chemical classes of kappa opioid receptor agonists, chroman-2-carboxamide derivatives and 2,3-dihydrobenzofuran-2-carboxamide derivatives, were synthesized. These agents exhibited high and selective affinity for the kappa opioid receptor. 相似文献
94.
95.
THOMAS JANSSEN KÅRE BREMER 《Botanical journal of the Linnean Society. Linnean Society of London》2004,146(4):385-398
Phylogenetic research on monocots has been extraordinarily active over the past years. With the familial interrelationships being sufficiently understood, the question of divergence times and crown node ages of major lineages comes into focus. In this study we present the first attempt to estimate crown and stem node ages for most orders and families of monocots, based on rbcL sequence data and comprehensive taxon sampling. From our analysis it is obvious that considerable monocot diversification took place during the Early Cretaceous, with most families already present at the Cretaceous–Tertiary boundary. Araceae, Arecaceae and Orchidaceae are among the oldest families with crown node ages reaching back into the Early Cretaceous. We comment on possible error sources and the necessity for methodological improvement in molecular dating. © 2004 The Linnean Society of London, Botanical Journal of the Linnean Society , 2004, 146 , 385–398. 相似文献
96.
L. A. GIGUÈRE 《Freshwater Biology》1986,16(4):557-560
SUMMARY. 1. Crop evacuation rates were estimated for the first time in Chaoborus larvae, using natural prey.
2. Fourth instar C. americanus Matheson digested copepods (Diaptomus leptopus S.A. Forbes) 48.7% faster than daphnids (Daphnia rosea Leydig) of similar size; meal size did not significantly affect the instantaneous rate of digestion (IRD) within each prey type. Prey specific IRD has not been reported before for zooplankton.
3. Prey specific differences in IRD require the use of natural prey when digestion experiments are to be used to estimate natural rates of food consumption of animals. 相似文献
2. Fourth instar C. americanus Matheson digested copepods (Diaptomus leptopus S.A. Forbes) 48.7% faster than daphnids (Daphnia rosea Leydig) of similar size; meal size did not significantly affect the instantaneous rate of digestion (IRD) within each prey type. Prey specific IRD has not been reported before for zooplankton.
3. Prey specific differences in IRD require the use of natural prey when digestion experiments are to be used to estimate natural rates of food consumption of animals. 相似文献
97.
Specific binding of the calcium antagonist [3H]verapamil to a microsomal fraction, a presumptive plasma membrane fraction and an intracellular membrane fraction of the phototactic unicellular green alga Chlamydomonas reinhardtii has been demonstrated. The specific activity of the plasma membrane marker enzyme K+-stimulated, Mg2+-dependent ATPase was severalfold higher in the upper (polyethylene glycol-rich) than in the lower (dextran-rich) phase, and the reverse was established for the marker enzymes of intracellular membranes such as cytochrome c oxidase for mitochondria and antimycin Aresistant NADPH-cytochrome c reductase for endoplasmic reticulum. Chlorophyll as a marker for thylakoid fragments was exclusively found in the lower phase. In the microsomal fraction two specific binding sites of [3H]verapamil were found at 22°C, one with higher and a second with lower affinity to [3H]verapamil. Separation of plasma membranes from intracellular membranes revealed that the highaffinity binding site is attributed to the plasma membrane fraction whereas the low-affinity binding site can be attributed to the intracellular membrane fraction. Specific binding to both separated membrane fractions is saturable and reversible. [3H]Verapamil binding to plasma membranes was not inhibited by the calcium channel blockers diltiazem and nifedipine. However, in the intracellular membrane fraction [3H]verapamil could be displaced by diltiazem but not by nifedipine. Increasing concentrations of calcium chloride inhibited [3H]verapamil binding in both fractions.Abbreviations Bmax
maximum density of binding sites
- BSA
bovine serum albumin
- Cyt.c
cytochrome c
- DTT
dithiothreitol
- EDTA
ethylenediaminetetraacetic acid
- EGTA
ethyleneglycol-bis(2-amino-ethylether)N,N-tetraacetic acid
- HEPES
N-2-hydroxyethylpiperazine-N-2-ethanesulfonic acid
- IC50
concentration causing 50% inhibition
- Mes
[N-morpholino]ethanesulfonic acid
- PEG
polyethylene glycol
- PMSF
phenylmethylsulfonylfluoride
- PVPP
polyvinylpolypyrrolidone
- TCA
trichloroacetic acid 相似文献
98.
Effects of Calcium Ions and of Calcium Channel Blockers on Galvanotaxis of Chlamydomonas reinhardtii
The effects of calcium ions and of the calcium channel blockers verapamil, diltiazem and nifedipine on galvanotaxis in Chlamydomonas have been investigated using a fully automated and computerized population system. Galvanotaxis is a function of the voltage applied to the cell population. However, the galvanotactic orientation also depends on the external calcium concentration. In a calcium-deprived nutrient medium which still contains 6 × 10?7M calcium, galvanotactic orientation is about 20% of orientation at optimal calcium concentration of 10?4 M at 9 V. The higher the external calcium concentration is, the lower is the voltage necessary for optimal galvanotactic orientation. The calcium channel blockers diltiazem and nifedipine likewise inhibit galvanotaxis of Chlamydomonas very specifically without impairing motility. Verapamil is effective, but also inhibits motility by causing detachment or shortening of the flagella. Nevertheless, inhibition of galvanotaxis by verapamil is not the only result of decreased motility, because the galvanotactic orientation is impaired to a greater extent than motility. The effectiveness of the three blockers tested in inhibiting galvanotaxis depends on the concentration and on the voltage applied. At 10?5 M, verapamil causes maximal inhibition of galvanotaxis at 9 V. At increasing concentrations up to 10?4 M, diltiazem inhibits galvanotaxis more strongly than the other blockers. If the voltage is varied at a constant blocker concentration of 2 × 10?5 M, nifedipine causes maximal inhibition at 3 V–6 V, diltiazem at 9 V and verapamil above 12 V. 相似文献
99.
KÅRE FOG 《Biological reviews of the Cambridge Philosophical Society》1988,63(3):433-462
(1) N added to decomposing organic matter often has no effect or a negative effect on microbial activity, at least in the long term. More than 60 papers are cited in support of this statement.
(2) The negative effect of N is mainly found with recalcitrant organic matter with a high C/N ratio (straw, wood, etc.), whereas a positive effect of N is common for easily degradable organic material with low C/N ratio.
(3) The negative effect of N could be explained by: (i) N disturbs the outcome of competition between potent and less potent decomposers; (ii) through 'ammonia metabolite repression', N blocks production of certain enzymes, at least in basidiomycetes, and enhances breakdown of the most available cellulose, whereby recalcitrant lignocellulose accumulates; (iii) amino compounds condense with polyphenols and other decomposition products, forming 'browning precursors' which are toxic or inhibitory.
(4) The effect of adding N may depend on the microflora present.
(5) There are indications that some microorganisms have a 'luxury uptake' of N when it is present in sufficient amounts, thereby delaying N mineralization.
(6) The addition of N seems to increase the formation of water-soluble , brown, recalcitrant compounds, but to decrease the amount of humus formed. 相似文献
(2) The negative effect of N is mainly found with recalcitrant organic matter with a high C/N ratio (straw, wood, etc.), whereas a positive effect of N is common for easily degradable organic material with low C/N ratio.
(3) The negative effect of N could be explained by: (i) N disturbs the outcome of competition between potent and less potent decomposers; (ii) through 'ammonia metabolite repression', N blocks production of certain enzymes, at least in basidiomycetes, and enhances breakdown of the most available cellulose, whereby recalcitrant lignocellulose accumulates; (iii) amino compounds condense with polyphenols and other decomposition products, forming 'browning precursors' which are toxic or inhibitory.
(4) The effect of adding N may depend on the microflora present.
(5) There are indications that some microorganisms have a 'luxury uptake' of N when it is present in sufficient amounts, thereby delaying N mineralization.
(6) The addition of N seems to increase the formation of water-soluble , brown, recalcitrant compounds, but to decrease the amount of humus formed. 相似文献
100.
Electrophysiological and biochemical responses of mouse vomeronasal receptor cells to urine-derived compounds: possible mechanism of action 总被引:1,自引:1,他引:0
Receptor cells of the vomeronasal organ (VNO) are thought to detect
pheromone-like molecules important for reproductive physiology. Several
compounds derived from male mouse urine have been demonstrated to affect
endocrine events in female mice. In the present study, the ability of these
compounds to affect VNO activity was tested. In dissociated VNO cells held
under voltage clamp conditions, application of dehydro-exo-brevicomin (DHB)
evoked an outward current at negative holding potentials and an inward
current at positive holding potentials. Under current clamp, DHB reduced
action potential firing. Since DHB application caused a decrease in
membrane conductance, this compound appeared to act by reducing inward
current through closing an ion channel. Biochemical experiments tested the
effects of DHB and 2- (sec-butyl)-4,5-dihydrothiazole (SBT) on cAMP levels
in the VNO. A mixture of DHB and SBT decreased cAMP levels in VNO sensory
tissue and had no effect on VNO non-sensory tissue. The results suggest
that pheromones have an inhibitory influence on action potential generation
and on cAMP levels in receptor cells of the VNO.
相似文献