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991.
A rare case of optic nerve entrance coloboma associated with situs inversus is reported. 相似文献
992.
Feitosa MF Rice T Rosmond R Rankinen T Leon AS Skinner JS Wilmore JH Bouchard C Rao DC 《Obesity research》2002,10(12):1222-1231
OBJECTIVE: To investigate familial basis for the relationship between cortisol adiposity at baseline and their training responses. RESEARCH METHODS AND PROCEDURES: Bivariate correlation and segregation analyses were employed between cortisol and several adiposity measures [body mass index, fat mass (FM), fat-free mass, percentage of body fat (% BF), abdominal visceral fat (AVF), abdominal subcutaneous fat (ASF), and abdominal total fat (ATF)] from 99 white families and 105 black families. RESULTS: In both races, significant inverse phenotypic correlations were generally observed between cortisol and adiposity measures at baseline but not for training responses. Significant cross-trait familial correlations were found for cortisol with abdominal fat (ASF, AVF, ATF) and overall body adiposity (FM, % BF) measures at baseline, which accounted for 14% to 20% of the phenotypic variance in whites. The cross-trait correlations were not significant for baseline phenotypes in blacks, perhaps because of the small sample size. A bivariate segregation analysis showed evidence of polygenic pleiotropy for cortisol with both abdominal fat and overall adiposity measures that accounted for 14% to 17% of the phenotypic covariance, but major gene pleiotropy was not suggested in whites. However, when ASF, AVF, and ATF were additionally adjusted for FM, no familial cross-trait correlations or polygenic pleiotropy between cortisol and the abdominal fat measures remained. DISCUSSION: Evidence was found for polygenic pleiotropy but not for pleiotropic major gene effects between cortisol and overall adiposity in whites. However, the covariation of cortisol with abdominal fat phenotypes is dependent on concomitant polygenic factors for total-body fat. 相似文献
993.
The damaging effects of noise on auditory function can be altered significantly by exposure to additional agents that may or may not by themselves be ototoxic. This chapter focuses on the ability of chemical asphyxiants present in both occupational settings and ambient environments to potentiate noise induced hearing loss in a laboratory animal model. Since the chemical agents under study do not produce permanent impairment of hearing by themselves, the finding of auditory impairment in excess of that which is produced by noise exposure alone can be defined as noise potentiation. This chapter focuses both on the exposure conditions that favour such potentiation and also on potential mechanisms for potentiation. The data show that low to moderate exposure levels of carbon monoxide (CO) and hydrogen cyanide can potentiate noise induced hearing loss (NIHL) and the relationship between such levels and those permitted in work environments is provided. Finally, evidence is presented that free oxygen radicals may be responsible for potentiation of NIHL by the chemical asphyxiants. First, the ability of a free radical spin trap agent, PBN, to prevent the adverse effects of CO is demonstrated. Then, in an additional experiment, electron paramagnetic spin resonance is used to demonstrate a high level of free radicals in the cochlea with combined exposure to CO + noise while individual exposures to CO and noise do not produce free radicals at levels detectable by this method. 相似文献
994.
Design,synthesis, structure-activity relationships,and molecular modeling studies of 2,3-diaryl-1,3-thiazolidin-4-ones as potent anti-HIV agents 总被引:4,自引:0,他引:4
Barreca ML Balzarini J Chimirri A De Clercq E De Luca L Höltje HD Höltje M Monforte AM Monforte P Pannecouque C Rao A Zappalà M 《Journal of medicinal chemistry》2002,45(24):5410-5413
Starting from 1H,3H-thiazolo[3,4-a]benzimidazoles (TBZs), we performed the design, synthesis, and the structure-activity relationship studies of a series of 2,3-diaryl-1,3-thiazolidin-4-ones. Some derivatives proved to be highly effective in inhibiting HIV-1 replication at nanomolar concentrations with minimal cytotoxicity, thereby acting as nonnucleoside HIV-1 RT inhibitors (NNRTIs). Computational studies were used to delineate the ligand-RT interactions and to probe the binding of the ligands to HIV-1 RT. 相似文献
995.
Intratumoral administration of paclitaxel in an in situ gelling poloxamer 407 formulation 总被引:6,自引:0,他引:6
In order to examine the efficacy of paclitaxel (Taxol, Bristol-Myers Squibb) after administration locally at the tumor site, we have developed a thermo-reversible gelling formulation in poloxamer 407 (Pluronic F-127) solution. Paclitaxel was incorporated in poloxamer 407 [20% (w/w)] at 0.5- and 1.0-mg/mL concentrations. The in vitro release studies were carried out in phosphate-buffered saline (pH 7.4) at 37 degrees C. Control and paclitaxel-poloxamer 407 formulations were administered intratumorally at a dose of 20 mg/kg in B16F1 melanoma-bearing mice. The change in tumor volume as a function of time and the survival of treated animals were used as measures of efficacy. Poloxamer 407 solution undergoes a reversible sol-gel transition when the temperature is raised to above 21 degrees C. In vitro paclitaxel release from poloxamer 407 gels was very slow (only 6.1% after 6 hr) probably due to the poor aqueous solubility of the drug. Significant enhancement in the anti-tumor efficacy was noted following intratumoral administration of paclitaxel-poloxamer 407 formulation. The initial tumor growth rate was delayed by 67% and the tumor volume doubling time was increased by 72% relative to saline control. In addition, more than 91% of the tumor-bearing animals that received paclitaxel in poloxamer 407 gel survived on day 15 post-administration as compared to 58% in the control group. The results of this study show significant benefit of paclitaxel for solid tumor when administered locally in an in situ gelling poloxamer 407 formulation. 相似文献
996.
前胡丙素对牛主动脉平滑肌细胞增殖的抑制作用 总被引:6,自引:0,他引:6
目的:探讨前胡丙素(pra-C)对牛主动脉平滑肌细胞(SMC)增殖的影响 方法:细胞DNA的合成量由~3H-胸腺嘧啶核苷[~3H]TdR)掺入试验测定,应用流式细胞术测定细胞周期,用乳酸脱氢酶活性测定观察药物的毒性.结果:无论有无血管紧张素Ⅱ(AngⅡ),在0.01μmol/L到10μmol/L浓度范围内,pra-C均可呈浓度依赖性地抑制SMC的增殖,抑制作用主要与阻止细胞进入有丝分裂期有关,而与细胞毒性无关.结论:pra-C能够完全阻断Aug Ⅱ诱导SMC的增殖效应,部分阻止小牛血清诱导的细胞分裂,这对于血管增生性疾病的防治有重要意义. 相似文献
997.
粉防己碱对心脏与血管重塑的影响 总被引:8,自引:0,他引:8
Rao MR 《Acta pharmacologica Sinica》2002,23(12):1075-1085
粉防己碱早年即已作为降压药应用,膜片箝及钙受体研究认为属特殊结构的钙拮抗剂.高血压患者80%伴左心室肥厚,此类患者发生心血管事件较高血压不伴心肌肥厚者高出8-10倍.本研究利用三种模型高血压(SHR,RHR,高肾素型;DOCA- salt HR 低肾素型)形成心肌血管重塑,研究了粉防己碱的防治疗效.粉防己碱灌胃9周后,明显减轻心脏(左室重/体重)血管(中膜厚度,壁/腔比值,血管横截面)重量及胶原含量,明显改善心脏血流动力学,特别改善心舒张功能,降低钙通道的受体密度,减少钙过负荷,增加心肌myosin等ATP酶活性,改善血管异常反应性,抑制血管增殖,诱导和敏化高血压大鼠血管平滑肌细胞凋亡,保护血管内皮功能,增加 NO产生.上述作用都促使心脏血管重塑得以逆转.因此是一个值得开发的既降压又防治心血管重塑的优秀药物. 相似文献
998.
A specimen of the sponge Myriastra clavosa from the Philippines contained two dimeric macrolides, clavosolides A and B. Clavosolide A is a symmetrical dimer, while clavosolide B is rendered unsymmetrical by the replacement of one of the methoxyl groups by a hydroxyl group. The structures of the clavosolides were elucidated by interpretation of spectroscopic data. 相似文献
999.
Gandhi M Rao K Chua S Saha V Lilleyman J Shankar A 《British journal of haematology》2003,122(3):451-453
Children who have completed treatment for acute lymphoblastic leukaemia (ALL) are commonly followed up for the first 5 years with regular full blood counts (FBCs) to monitor for relapse of disease. There is little evidence to suggest that this practice improves the detection rate of unexpected relapse. Surveillance FBCs, performed on 43 children with relapsed ALL between 1990 and 1999, were analysed. Of the 42 relapses in children off therapy, only two were detected by an abnormal FBC. Routine FBCs in asymptomatic children off therapy lacks specificity in detecting unexpected relapses and maybe safely discontinued. 相似文献
1000.