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81.
Infectivity of preserved Cryptosporidium parvum oocysts for immunosuppressed adult mice 总被引:1,自引:0,他引:1
Shiguang Yang Mark C. Healey Chunwei Du 《FEMS immunology and medical microbiology》1996,13(2):141-145
Abstract The present study was undertaken to determine the infectivity of Cryptosporidium parvum oocysts for immunosup-pressed adult C57BL/6N mice after the oocysts had been stored from 1–48 months at 4°C in 2.5% potassium dichromate. All mice inoculated with oocysts 1–18 months old developed patent infections, while mice inoculated with older oocysts remained uninfected. The prepatent period was extended from 2 to 6 or 7 days as the storage time for oocysts increased. The finding that C. parvum oocysts remain infective for mice for at least 18 months offers important economic and time-saving advantages for investigators who frequently require large numbers of oocysts that must be painstakingly purified from calf manure. 相似文献
82.
本实验采用D-氨基半乳糖(D-GalN)诱导的大鼠急性肝损伤模型,观察大鼠肝脏组织化学的变化,探讨肝炎平对急性肝损伤的保护作用。实验分为四组,即正常对照组、模型组、肝炎平及肝得健保护组。结果表明:肝炎平对肝细胞膜系统有一定的保护作用。肝炎平组和肝得健组SDH、CCO及ChE活性明显高于模型组,且与正常对照组相近。本实验模型组ACP的活性明显高于正常组,而肝炎平组ACP的活性明显低于模型组,与正常对照组无显著性差异。提示:肝炎平可显著改善因D-氨基半乳糖所致肝损害的作用。且其对肝细胞的保护作用与肝得健一致。 相似文献
83.
中药固真方对一些与细胞增殖有关基因表达的影响姚明忠,顾文聪,丁卫,韩志芬,杜国光(上海中医药大学生物化学教研室,上海200032)(北京医科大学生物化学与分子生物学系,北京100083)中药固真方(VRF)具有补肾益精、延缓衰老的作用[1].能提高成... 相似文献
84.
Forskolin(FSK)是一种植物二萜类化合物,为腺苷酸环化酶的特异激活剂,实验发现:FSK和作为参照的诱导分化剂维甲酸(RA)单独或联合应用均可升高胞浆蛋白激酶C(PKC)活性,并降低膜PKC活性,FSK可使表皮生长因子(EGF)诱导的细胞内三磷酸肌醇(IP3-1,4,5)水平降低至对照组的44.4%至67%;FSK与RA合用可显著降低成骨样细胞特征蛋白碱性磷酸酶(AKP)的活性。以上结果表明,FSK对成骨样细胞内磷脂酰肌醇信息传递体系有深刻影响,可能与其调节细胞的增殖分化有关。 相似文献
85.
86.
大鼠不同脑区突触体钙水平的年龄差异 总被引:10,自引:1,他引:9
本实验使用荧光指示剂Fura-2与Tb~(3+),检测了不同年龄组大鼠的不同脑区(海马、皮层、间脑、小脑)突触体内游离钙与膜结合钙水平。结果显示,与青年对照组相比,老年大鼠大部分脑区(海马、皮层、间脑)突触体内游离钙水平显著增高,尤其是海马突触体内游离钙增高极为显著;其突触体膜结合钙水平表现为:海马、小脑两脑区明显升高,而皮层、间脑两脑区明显下降,呈现一种全脑范围内的钙水平失衡。提示动物的衰老与其脑内钙自体平衡失调有关。 相似文献
87.
The 3-D structure of a zinc metallo-beta-lactamase from Bacillus cereus reveals a new type of protein fold. 总被引:4,自引:0,他引:4
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A Carfi S Pares E Duée M Galleni C Duez J M Frère O Dideberg 《The EMBO journal》1995,14(20):4914-4921
The 3-D structure of Bacillus cereus (569/H/9) beta-lactamase (EC 3.5.2.6), which catalyses the hydrolysis of nearly all beta-lactams, has been solved at 2.5 A resolution by the multiple isomorphous replacement method, with density modification and phase combination, from crystals of the native protein and of a specially designed mutant (T97C). The current model includes 212 of the 227 amino acid residues, the zinc ion and 10 water molecules. The protein is folded into a beta beta sandwich with helices on each external face. To our knowledge, this fold has never been observed. An approximate internal molecular symmetry is found, with a 2-fold axis passing roughly through the zinc ion and suggesting a possible gene duplication. The active site is located at one edge of the beta beta sandwich and near the N-terminal end of a helix. The zinc ion is coordinated by three histidine residues (86, 88 and 149) and a water molecule. A sequence comparison of the relevant metallo-beta-lactamases, based on this protein structure, highlights a few well-conserved amino acid residues. The structure shows that most of these residues are in the active site. Among these, aspartic acid 90 and histidine 210 participate in a proposed catalytic mechanism for beta-lactam hydrolysis. 相似文献
88.
Thomas J. Thekkumkara Jing Du John C. Zwaagstra Kathleen M. Conrad John Krupinski Kenneth M. Baker 《Molecular and cellular biochemistry》1995,152(1):77-86
G-protein coupled Angiotensin II receptors (AT1A), mediate cellular responses through multiple signal transduction pathways. In AT1A receptor-transfected CHO-K1 cells (T3CHO/AT1A), angiotensin II (AII) stimulated a dose-dependent (EC50=3.3 nM) increase in cAMP accumulation, which was inhibited by the selective AT1, nonpeptide receptor antagonist EXP3174. Activation of protein kinase C, or increasing intracellular Ca2+ with ATP, the calcium ionophore A23187 or ionomycin failed to stimulate cAMP accumulation. Thus, AII-induced cAMP accumulation was not secondary to activation of a protein kinase C- or Ca2+/calmodulin-dependent pathway. Since cAMP has an established role in cellular growth responses, we investigated the effect of the AII-mediated increase in cAMP on cell number and [3H]thymidine incorporation in T3CHOA/AT1A cells. AII (1 M) significantly inhibited cell number (51% at 96 h) and [3H]thymidine incorporation (68% at 24 h) compared to vehicle controls. These effects were blocked by EXP3174, confirming that these responses were mediated through the AT1 receptor. Forskolin (10 M) and the cAMP analog dibutyryl-cAMP (1 mM) also inhibited [3H]thymidine incorporation by 55 and 25% respectively. We extended our investigation on the effect of AII-stimulated increases in cAMP, to determine the role for established growth related signaling events, i.e., mitogen-activated protein kinase activity and tyrosine phosphorylation of cellular proteins. AII-stimulated mitogen-activated protein kinase activity and phosphorylation of the 42 and 44 kD forms. These events were unaffected by forskolin stimulated increases in cAMP, thus the AII-stimulated mitogen-activated protein kinase activity was independent of cAMP in these cells. AII also stimulated tyrosine phosphorylation of a number of cellular proteins in T3CHO/AT1A cells, in particular a 127 kD protein. The phosphorylation of the 127 kD protein was transient, reaching a maximum at 1 min, and returning to basal levels within 10 min. The dephosphorylation of this protein was blocked by a selective inhibitor of cAMP dependent protein kinase A, H89-dihydrochloride and preexposure to forskolin prevented the AII-induced transient tyrosine phosphorylation of the 127 kD protein. These data suggest that cAMP, and therefore protein kinase A can contribute to AII-mediated growth inhibition by stimulating the dephosphorylation of substrates that are tyrosine phosphorylated in response to AII. 相似文献
89.
90.