胆结石对肝脏细胞钙稳态影响与调整的实验研究

用低蛋白饮食方法建立豚鼠胆色素结石模型，共设对照、致石、维生素Ｃ修复、丹参修复和对照修复等５组，规定时间内处死动物，用放射免疫、固相酶联免疫、生物化学等方法检测肝细胞内环—磷酸腺甙（ｃＡＭＰ）、环—磷酸鸟嘌呤（ｃＧＭＰ）、钙调素（ＣａＭ）、钙，三磷酸腺甙酶（Ｃａ２＋－ＡＴＰａｓｅ）、磷酸化酶ａ等水平。致石组豚鼠肝脏细胞内ｃＡＭＰ和磷酸化酶ａ升高，而ｃＧＭＰ，ＣａＭ和Ｃａ２＋－ＡＴＰａｓｅ下降，表明肝细胞钙稳态呈失调状态。维生素Ｃ和丹参可调整肝细胞的上述改变，说明维生素Ｃ和丹参具有维持肝细胞钙稳态的作用。     

糖尿病妇科手术92例的围手术期处理

2002-01／2004-01Ⅱ型糖尿病(DM)妇科手术患92例，年龄31～73(平均53．4)岁．有明确DM病史53例．病程1／12～21(平均6．9)a，入院后新诊断的DM39例空腹血糖为5．9—18．0(平均9．6)mmol/L，餐后血糖为9．3—22．6(平均16．5)mmol/L，术前准备时间平均为6．4d，术后住院时间平均为11．4d，术前有并存症72例．随机抽取同期住院非DM妇科手术92例，年龄22～65(平均41．5)岁，     

基质金属蛋白酶及微血管密度和子宫内膜癌的关系

基质金属蛋白酶及其抑制剂在子宫内膜癌的侵袭和转移中发挥着重要的作用。肿瘤的新生血管对肿瘤的发生、发展、转移及预后有着重要作用。微血管密度是衡量血管生成的定量指标。基质金属蛋白酶抑制剂可抑制血管的生成和MMPs对细胞外基质的降解。现将他们与子宫内膜癌的关系综述如下。     

下腹部多个真皮下血管网皮瓣在手外伤修复中的应用

目的：应用下腹部多个真皮下血管网皮瓣修复手外伤，方法：在下腹形成以旋髂浅血管为蒂的髂腰部皮瓣及以腹壁浅血管为蒂的下腹部皮瓣，二皮瓣共蒂形成双叶皮瓣，同时将其修薄，形成有轴心血管的真皮下血管网皮瓣，修复两指完全脱套伤。在下腹部形成多个真皮下血管网的任意皮瓣，修复多个指背皮肤缺损伴有肌腱及骨外露的创面。供区如不能直接拉拢缝合，可取断层皮片修复供区创面.结果：本组10例中，8例采用下腹部双叶真皮下血管网轴型皮瓣修复，2例采用下腹部真皮下血管网任意皮瓣修复，术后效果。结论：采用多个真皮下血管网皮瓣修复手外伤的创面，伤指不需并指，去脂，分指，术后外形佳，是目前较理想的修复手外伤的手术方法。     

隐动脉筋膜蒂的交腿皮瓣修复小腿严重软组织缺损

目的探讨一种小腿严重软组织缺损的修复方法。方法以健侧隐动脉为蒂的顺行或逆行交腿皮瓣修复患侧小腿软组织缺损。结果本组8例均有效地覆盖受区创面,随访三个月,皮瓣全部成活。结论该皮瓣不牺牲小腿的重要血管,质地与受区相似,方法简单易行,血运可靠,血管蒂长,是修复小腿严重软组织缺损的较好方法。     

九连山自然保护区冬青属植物资源的初步研究

通过对九连山自然保护区冬青属植物资源的调查研究，发现保护区内共有34种(包括变种)冬青属植物，其中8种为江西新分布，其垂直分布范围较广，以海拔800m以下最为集中。与邻近山体冬青属植物比较结果表明谈属内不同种的数量存在差异。     

骨骺牵张与骨骺板的生物力学性质

本研究是对新西兰幼兔股骨远端骨骺进行体内和体外牵张实验.16只兔右股骨经5～10N力每3天一次牵张.4周后的股骨长度值明显大于左侧和0N组.形态学变化是受牵张的骺板增厚,软骨细胞增殖且无骨骺分离骨折.体外骺板抗断裂测试显示夸张后的骺板强度不低于未经牵张的对照侧.8只动物16根股骨于体外接受20～100N力的牵张,其骺板的塑性变形度随牵张力值的增高而增大,抗断裂强度亦不低于未经牵张的骨骺.这些结果表明适量的牵张力和/或低牵张速率是实现“软骨分离”或骨延长的关键.     

Inhibition of CDK activity and PCNA-dependent DNA replication by p21 is blocked by interaction with the HPV-16 E7 oncoprotein

p21 inhibits cyclin-dependent kinase (CDK) activity and proliferating cell nuclear antigen (PCNA)-dependent DNA replication by binding to CDK/cyclin complexes and to PCNA through distinct domains. The human papillomavirus (HPV)-16 E7 oncoprotein (16E7) abrogated a DNA damage-induced cell cycle arrest in vivo, despite high levels of p21. Using cell lysates and purified proteins we show that 16E7 prevented p21 both from inhibiting CDK2/cyclin E activity and PCNA-dependent DNA replication, whereas the nononcogenic HPV-6 E7 had reduced effects. Inactivation of both inhibitory functions of p21 was attained through binding between 16E7 and sequences in the carboxy-terminal end of p21 that overlap with the PCNA-binding site and the second p21 cyclin-binding motif. These data imply that the carboxyl terminus of p21 simultaneously modulates both CDK activity and PCNA-dependent DNA replication and that a single protein, 16E7, can override this modulation to disrupt normal cell cycle control.     

解剖钢板结合连续被动运动功能锻炼治疗胫骨平台骨折

目的 评价解剖钢板结合连续被动运动(CPM)功能锻炼在治疗胫骨平台骨折中的应用价值.方法 2003年5月至2005年10月本院34例胫骨平台骨折行解剖复位、解剖钢板内固定并在术后进行CPM功能锻炼.结果 术后对患者行X线检查示骨折实现解剖复位或接近解剖复位.23例患者经5～30个月随访骨折均愈合,无植骨坏死发生.CPM功能锻炼后运动功能恢复优良率为82.6%(19/23).结论 采用关节面的解剖复位、解剖钢板及牢固固定后配合术后CPM功能锻炼对于胫骨平台骨折有很好的疗效.     

Spectral karyotyping combined with locus-specific FISH simultaneously defines genes and chromosomes involved in chromosomal translocations

Genes that play roles in malignant transformation have often been found proximate to cancer-associated chromosomal breakpoints. Identifying genes that flank chromosomal reconfigurations is thus essential for cancer cytogenetics. To simplify and expedite this identification, we have developed a novel approach, based on simultaneous spectral karyotyping and fluorescence in situ hybridization (FISH) which, in a single step, can identify gross chromosomal aberrations as well as detect the involvement of specific loci in these rearrangements. Signals for specifically queried genes (FISH probe) were easily detectable in metaphase cells, together with the signals from painted chromosomes (spectral karyotyping probes). The concentration and size of the FISH probes could cover a wide range and still be used successfully. Some of the nucleotide-bound dyes used for the labeling, as Cy3, Spectrum Orange, Alexa 594, Texas Red, and Rhodamine 110, were particularly efficient. More than one gene can be queried in the same metaphase, because multiple FISH probes could be hybridized simultaneously. To demonstrate this technique, we applied it to the myeloma cell line Karpas 620, which has numerous chromosomal rearrangements. The approach that we present here will be particularly useful for the analysis of complex karyotypes and for testing hypotheses arising from cancer gene expression studies. Published 2000 Wiley-Liss, Inc.