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1.
答:这里的[H]并不是指氢离子(H+),而是指辅酶中的氢(还原性氢),[H]的产生与利用即NADH、FADH。和NADPH的产生与利用。光合作用与呼吸作用中产生和利用的[H]不同,光合作用产生及利用NADPH.而呼吸作用产生与利用的[H]主要是NADH与FADH2。  相似文献   

2.
Homocysteine plays a key role in several pathophysiological conditions. To assess the methionine–homocysteine kinetics by stable isotope methodology, we developed a simultaneous quantification method of [2H7]methionine, [2H4]methionine, methionine, [2H4]homocysteine and homocysteine in rat plasma by gas chromatography–mass spectrometry (GC–MS). [13C]Methionine and [13C]homocysteine were used as analytical internal standards to account for losses associated with the extraction, derivatization and chromatography. For labeled and non-labeled homocysteine measurements, disulfide bonds between homocysteine and other thiols or proteins were reduced by dithiothreitol. The reduced homocysteine and methionine species were purified by cation-exchange chromatography and derivatized with isobutyl chlorocarbonate in water–ethanol–pyridine. Quantification was carried out by selected ion monitoring of the molecular-related ions of N(O,S)-isobutyloxycarbonyl ethyl ester derivatives on the chemical ionization mode. The intra- and inter-day precision of the assay was less than 6% for all labeled and non-labeled methionine and homocysteine species. The method is sensitive enough to determine pharmacokinetics of labeled methionine and homocysteine.  相似文献   

3.
李森 《生物学通报》2011,46(5):23-24
光合作用与呼吸作用所涉及的[H]指NADH、FADH2与NADPH中的还原性氢。光合作用与呼吸作用中产生和利用的[H]不同,光合作用产生及利用NADPH,而呼吸作用产生与利用的[H]主要是NADH与FADH2。  相似文献   

4.
周洁  黄大有  刘鼎新 《生理学报》1994,46(5):488-494
本研究应用[3H]cortisol和[3H]dexamethasone(DEX)两种配基,观察到大鼠肝细胞膜上存在一类糖皮质激素(GC)特异结合位点。这些位点与GC的结合具有饱和性、高亲和力及低容量。其平衡解离常数(Kd)分别为12.84±6.58nmol/L和40.27±23.44nmol/L;最大结合容量(Bmax)分别为2.57±1.84pmol/mg蛋白质与0.64±0.18pmol/mg蛋白质(cortisol,n=4;DEX,n=3;±SE)。动力学实验数据所得的Kd值与Scatchard分析所得的Kd值结果基本一致。[3H]cortisol和[3H]DEX饱和结合实验数据用Scatchard作图分析,均显示为直线。Hill系数则分别为0.9880和0.9990.竞争抑制实验结果表明,cortisol对[3H]cortisol的结合位点有高度特异性竞争,比其它几种类固醇(强的松、黄体酮、RU486、DEX)的竞争力至少强40倍以上.用放射自显影技术进行研究,也提供了[3H]cortisol特异结合银粒位于大鼠肝细胞膜上的依据。  相似文献   

5.
The binding of nonselective α1- and β-adrenoreceptor antagonists [3H]prazosin and [3H]dihydroalprenolol ([3H]DHA) to rat cerebral cortex synaptosomal membranes has been studied. It is found that ligand-receptor interactions of α1-adrenoreceptors fit into a single receptor pool model, which assumes the binding of two ligand molecules to one receptor molecule. The parameters of [3H]prazosin binding to α1-adrenoreceptors are as follows: K d = 2.58 ± 0.20 nM; B m = 2.95 ± 1.12 fmol/mg protein; Hill coefficient, n = 2. For β-adrenoreceptors, ligand-receptor interactions fit into a model assuming the presence of two receptor pools in the same effector system and binding of two ligand molecules to one receptor molecule. The corresponding parameters of the [3H]DHA binding to β-adrenoreceptors are as follows: K d1 = 0.74 ± 0.09 nM; K d2 = 7.63 ± 0.70 nM; B m1 = 25 ± 2 fmol/mg, B m2 = 48 ± 2 fmol/mg, n 1 = 2; n 2 = 2. We suggest that in rat cerebral cortex membranes α-and β-adrenoreceptors exist as dimers.  相似文献   

6.
Mouse isolated vas deferens preincubated with [3-H]noradrenaline was superfused and the effect of 1-adrenoceptor agonists was studied on the release of total radioactivity ([3H]noradrenaline +3H-metabolites) and [3H]noradrenaline. Reverse phase high pressure liquid chromatography (HPLC) combined with scintillation spectrometry was used to separate [3H]noradrenaline from its metabolites. Among the 1-adrenoceptor agonists (1-phenylephrine, ST-587(2-(2-chloro-5-trifluoromethyl phenylimino)-imidazole), (–)-amidephrine, methoxamine, cirazoline and l-noradrenaline) studied l-phenylephrine, ST-587 and l-noradrenaline were capable of releasing3H-noradrenaline. The effect of noradrenaline was stereospecific. As determined by HPLC combined with scintillation spectrometry the release of total radioactivity in response to l-noradrenaline is mainly due to [3H]noradrenaline. It is suggested that l-noradrenaline, l-phenylephrine, and ST-587 in addition to their direct effect on different receptors they also have indirect action through the release of noradrenaline which might be partly involved in the pharmacological responses. The mechanisms whereby l-noradrenaline and l-phenylephrine release noradrenaline would appear to involve a saturable Ca-independent and a cocaine and temperature sensitive process. On the basis of our findings among the 1-adrenoceptor agonist studied (–)-amidephrine, methoxamine and cirazoline is a better choice than l-phenylephrine or ST-587 for selective stimulation of postjunctional 1-adrenoceptor, they do not release noradrenaline.  相似文献   

7.
An efficient and novel method for the preparation of spiro[pyrazolo[4,3-d]pyrimidin]-7′(1′H)-ones by the condensation of 4-amino-1-methyl-3-propylpyrazole-5-carboxamide with ketones under mild conditions using catalytic InCl3 was reported. This method has been extended for the synthesis of novel spiro[benzo[4,5]thieno[2,3-d]pyrimidine-2,3′-indoline]-2′,4(3H)-dione which are having potential applications in medicinal chemistry. All the synthesized compounds were evaluated for their anti-proliferative properties in vitro against cancer cell lines and several compounds were found to be active. Further in vitro studies revealed that inhibition of sirtuins could be the possible mechanism of action of these molecules.  相似文献   

8.
To identify structurally novel corticotropin-releasing factor 1 (CRF(1)) receptor antagonists, a series of bicyclic core analogs pyrrolo[1,2-b]pyridazines and pyrrolo[2,1-f]triazin-4(3H)-ones, which were designed based on a monocyclic core antagonist, was synthesized and evaluated. Among the compounds tested, 2-difluoromethoxy-4-methylpyridin-5-yl analog 27 was found to show efficacy in a dose-dependent manner in an elevated plus maze test in rats. The discovery process and structure-activity relationship is presented.  相似文献   

9.
Abstract

Nucleophilic substitution reactions of 4-azolyl-1 β-P-D-ribofuranosylpyrimidin-2(1H)-one and 6-azolyl-9-β-D-ribofuranosyl-9H-purine derivatives, which were converted from uridine and inosine, with [15N]phthalimide in the presence of triethylamine or DBU gave N 4-phthaloyl[4-15N]cytidine and N 6-phthaloyl[6-15N]- adenosine derivatives, respectively, in high yields. Similar reactions of those azolyl derivatives with succinimide afforded N 4-succinylcytidine and N 6-succinyladenosine derivatives in high yields. The corresponding 2′-deoxyribonucleosides were also synthesized efficiently through the same procedure.

  相似文献   

10.
应用微细胞检测基因产物的方法由于质粒和噬菌体等的DAN分子能在细胞内进行自我复制,以及DNA重组技术的普及,质粒DNA做为异源性DNA分子的载体,在基因工程中目前已被广泛应用。在克隆或分析真核生物或原核生物的多种不同基因时,常用检测基因表达来确定其存在。把含有某一目的基因的DNA片段和载体质粒的DNA进行重组,再通过重组DNA在受体细胞中的转录、翻译、  相似文献   

11.
Chemically modified DNA oligonucleotides have been crucial to the development of antisense therapeutics. High-resolution structural studies of pharmaceutically relevant derivatives have been limited to only a few molecules. We have used NMR to elucidate the structure in solution of two DNA-RNA hybrids with the sequence d(CCTATAATCC).r(GGAUUAUAGG). The two hybrids contain an unmodified RNA target strand, whereas the DNA strand contains one of two different stereoregular sugar-phosphate backbone linkages at each nucleotide: 1), [Rp]-phosphorothioate or 2), [Sp]-phosphorothioate. Homonuclear two-dimensional spectroscopy afforded nearly complete nonlabile proton assignments. Distance bounds, calculated from the nuclear Overhauser effect (NOE) crosspeak intensities via a complete relaxation matrix approach with the program MARDIGRAS, were used to restrain the structure of the two hybrids during simulations of molecular dynamics. Analysis of restrained molecular dynamics trajectories suggests that both hybrids are flexible, requiring the use of molecular dynamics with time-averaged restraints (MDtar) to generate ensembles of structures capable of satisfying the NMR data. In particular, the deoxyribose sugars of the DNA strand show strong evidence of repuckering. Furthermore, deoxyribose sugar repuckering is accompanied by increased flexibility of overall helical geometry. These observations, together with the analysis of the crystal structure of a hybrid duplex in complex with ribonuclease H (RNase H), suggested that this flexibility may be required for recognition by RNase H.  相似文献   

12.
This paper describes a [15N,1H]/[13C,1H]-TROSY experiment for the simultaneous acquisition of the heteronuclear chemical shift correlations of backbone amide 15N–1H groups, side chain 15N–1H2 groups and aromatic 13C–1H groups in otherwise highly deuterated proteins. The 15N–1H and 13C–1H correlations are extracted from two subspectra of the same data set, thus preventing possible spectral overlap of aromatic and amide protons in the 1H dimension. The side-chain 15N–1H2 groups, which are suppressed in conventional [15N,1H)-TROSY, are observed with high sensitivity in the 15N–1H subspectrum. [15N,1H]/[13C,1H]-TROSY was used as the heteronuclear correlation block in a 3D [1H,1H]-NOESY-[15N,1H]/[13C,1H]-TROSY experiment with the membrane protein OmpA reconstituted in detergent micelles of molecular weight 80000 Da, which enabled the detection of numerous NOEs between backbone amide protons and both aromatic protons and side chain 15N–1H2 groups.  相似文献   

13.
Abstract

The ionic and drug specificities of the [3H]nifedipine binding site in rabbit cardiac homogenates were investigated. Divalent cations inhibited specific [3H]nifedipine binding in the potency order: Ni+2 > Ca+2 ≥ Mg+2. Monovalent cations did not affect binding. The inorganic calcium entry blocker La+3 (IC50 = 1.1 mM) was the most potent cation in inhibiting radioligand binding. Calcium entry blocking drugs of different chemical classes inhibited [3H]-nifedipine binding, with a rank potency order of: nifedipine >> D600 = verapamil > tiapamil > cinnarizine = prenylamine. The same potency order was observed for these drugs in inducing negative inotropic activity of isolated, electrically stimulated rabbit papillary muscle. The stereoselectivity of verapamil and D600 ((?) >> (+) isomers) in depressing papillary muscle contractions was not seen in [3H]nifedipine competition experiments. This presents an obstacle to accepting the equivalence of the [3H]nifedipine binding site with the myocardial Ca+2 channel. It is, however, possible that the myocardial Ca+2 channel may be associated with multiple sites of action for calcium entry blockers.  相似文献   

14.
15.
M. Fischer 《BioControl》1971,16(1):101-109
Zusammenfassung Doryctes molorchi wird neu beschrieben,Doryctes petrovskii Kokujew wird redeskribiert. Ersterer ist ausMolorchus umbellatarum Schreber, letzterer ausPogonochaerus hispidus L. (Col., Cerambycidae) gezogen. Beide Arten sind neu für ?sterreich. Der Bestimmungsschlüssel für die pal?arktischenDoryctes-Arten nachTelenga wird erweitert.
Summary Doryctes molorchi is described as new andD. petrovskii Kokujew is redrescribed. The former is reared fromMolorchus umbellatarum Schreber, the latter fromPogonochaerus hispidus L. (Col., Cerambycidae). The species are new to the fauna of Austria. A key for identification of the palearcticDoryctes species afterTelenga (1941) is given.


Die Untersuchungen wurden mit Unterstützung des Fonds zur F?rderung der wissenschaftlichen Forschung durchgeführt.  相似文献   

16.
[~3H]2-脱氧葡萄糖定量研究方法的介绍   总被引:1,自引:0,他引:1  
2-脱氧葡萄糖(2-DG)方法是一种新的形态与功能结合的神经科学研究方法。我们在现有条件下对此方法的应用做了一些研究。在实验中,我们采用了股静脉注射[~3H]标记的2-DG,测定血糖、血液中放射性物质含量及用显微分光光度计测定放射自显影片光密度的方法,并采用 Sokoloff 的计算公式计算各脑区的葡萄糖代谢率。  相似文献   

17.
18.
The biodistribution of [75Se]BISTAES was studied in guinea pigs. A higher concentration of radioactivity was observed in articular cartilage than in other tissues or organs. A minimal amount of radioactivity was found in the blood, muscle and bone. The compound was excreted rapidly in urine. The target to background ratios were encouraging. [75Se]BISTAES has potential as an articular cartilage imaging agent and further studies in osteoarthritic animals are merited.  相似文献   

19.
P. Cochereau 《BioControl》1970,15(3):281-285
Résumé La TachinaireMicrophthalma europaea Egg., parasite de larves deScarabaeidae en Afrique du Nord [Hurpin & Fresneau, 1964] a été multipliée à Nouméa (Nouvelle-Calédonie) sur un nouvel h?te de substitutionProtaetia fusca Hrbt. (Cetoniinae). Cet h?te nouveau permet maińtenant un élevage massif du parasite en Nouvelle-Calédonie, avant sa libération éventuelle à l'?le Wallis contre les larves d'Oryctes rhinoceros L., unDynastinae ravageur du cocotier.
Summary The Tachinid fly,Microphthalma europaea Egg., parasite onScarabaeidae larvae in North Africa (Hurpin & Fresneau, 1964) was multiplied in Noumea (New Caledonia) on a new alternative hostProtaetia fusca Hrbt. (Cetoniinae). The contingent introduction of this parasite fly to Wallis island against larvae ofOryctes rhinoceros L. (Dynastinae), the coconut rhinoceros beetle, so could be now more easy from New Caledonia.


Nous remercions le DrP. Jourdeuhil, Directeur de la Station de Lutte Biologique d'Antibes (France), d'avoir bien voulu lire notre manuscrit et nous apporter ses conseils les plus judicieux.  相似文献   

20.
记述云南高黎贡山[虫脩]目异[虫脩]科和[虫脩]科5个新种,即刺胸阿异[虫脩]Aruanoidea notata,sp.nov.,高山短肛[虫脩]Baculum altissimum,sp.nov.,光亮拟短肛[虫脩]Parabaculum laevigatum,sp.nov.,双角刺[虫脩]Cnipsomorpha biangulatus,sp.nov.,黑缘介[虫脩]Interphasma marginatum,sp.nov.,并且首次记述了污色无翅刺蟾Cnipsomorpha colorantis(Chen et He)的雄性。模式标本分别存放于北京林业大学与中国林业科学研究院昆虫标本馆。  相似文献   

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