腕部广泛损伤的修复与康复治疗

报道30例腕部损伤患者,伤情比较相同。其中12例采用传统外科手术治疗,不作或仅作不正规的理疗;18例采用显微外科技术治疗,仔细修复各种组织结构,术后系统地进行康复治疗。经随访3个月～2年,传统方法治疗组优良率仅为8.3％;采用显微外科技术及康复治疗组优良率达67％。     

Lower heat shock factor activation and binding and faster rate of HSP-70A messenger RNA turnover in heat sensitive human leukemias.

Normal bone marrow progenitors and some leukemic cells develop only a limited amount of thermotolerance. Further, once developed, thermotolerance decays at a faster rate than that normally observed in cells of nonhemopoietic origin. Thermotolerance induction and maintenance correlates with reduced levels of expression of various M(r) 70,000 heat shock proteins (HSP-70) mRNAs after heat shock. We have now compared the accumulation of HSP-70 proteins in heat-shocked human leukemic cells KG-1, HL-60, and K562 to that in Ht1080, a colon carcinoma cell line. We have found reduced accumulation of HSP-70 proteins in all leukemic cells. The rate of decay of HSP-70A mRNA, measured following heat shock by using actinomycin D treatment to inhibit further RNA synthesis, was more rapid in KG-1 and HL-60 cells compared to Ht1080 cells. The half-life of HSP-70A mRNA was 2 h in KG-1 and HL-60 cells while in Ht1080 cells it was > 7 h. HSP-70A mRNA is known to decay with a half-life of 2 h in unheated cells; this is increased to > 7 h following heat shock. We therefore postulate that leukemic cells lack the mechanism to stabilize HSP-70A mRNA after heat shock. One postulated mechanism for HSP-70 mRNA decay rate is known to be due to the nucleotide sequences at the 3'-untranslated region. We examined the 3'-untranslated region in leukemic cells. No sequence variations, however, were observed at either the genomic or the complementary DNA levels between leukemic or nonleukemic tumor cells. Heat shock factor activation and binding by gel retardation assays showed that KG-1 and HL-60 cells had a reduced heat shock factor binding to the heat shock element when compared to K562 and Ht1080 cells. Furthermore, HSF-1 mRNA was found to be expressed at relatively lower levels in HL-60 cells when compared to Ht1080 or KG-1 cells. In conclusion, reduced HSP synthesis and accumulation of leukemic cells after heat shock correlates with the reduction in heat shock factor-heat shock element binding and a faster HSP-70A mRNA decay rate that is observed in these cells.     

医源性子宫内膜异位症的治疗进展

医源性子宫内膜异位症是指由于医学检查或治疗的影响而使子宫内膜异位种植，存活或已有的内膜异位灶进一步发展，近年发病率逐渐上升，原因主要与各种妇产科操作的增多有关，现就医源性子宫内膜异位症的治疗进展作一综述。     

美维松对膈肌功能的影响

目的：研究不同剂量美维松对膈肌和拇收肌的抑制时程与恢复过程。方法：３０例ＡＳＡⅠ级的成年手术患者，按美维松用量分成两组，Ⅰ组：０．１６ｍｇ／ｋｇ，Ⅱ组：０．２０ｍｇ／ｋｇ，每组１５例。同步测定跨膈肌压（Ｐｄｉ）和拇收肌对连续四次刺激（ＴＯＦ）反应的Ｔ１（ＡＰＴ１）及ＴＯＦｒ值。结果：显示两组ＡＰＴ１最大抑制相近，是Ｐｄｉ的１．７倍。Ｐｄｉ达到最大抑制及恢复到７５％的时间比ＡＰＴ１快得多。结论：提示美维松对膈肌收缩功能的抑制比拇收肌差，但恢复迅速。     

海绵状血管瘤内压监测指导栓塞及硬化剂注射治疗

为探讨在栓塞硬化海绵状血管瘤中瘤腔内变化规律及其意义，在２９例治疗过程中给机械性减缓交界本静脉回流，进行了瘤腔内压连续监测，发现：瘤腔基础内压力０．６６７～２．０ｋＰａ（１ｋＰａ＝７．５ｍｍＨｇ）。颈部最低，回流快者所需栓塞次数多，用量大，瘤腔内压力曲线在栓塞初始为平台波形，提示回流静脉逐一被栓塞，随后出现缓慢下降的印峰波形，去除瘤体表浅回流静脉机械性压迫，瘤腔内压不变，提示回流静脉全部栓塞，可注     

Immunization strategies for the production of rat monoclonal anti-idiotope antibodies

Anti-idiotypic antibodies are powerful reagents for the study of immunoregulation, and have potential interest as vaccines against tumors and infectious diseases. Three immunization strategies for the production of rat monoclonal anti-idiotope antibodies have been compared in this paper. Male Wistar rats were immunized i.p. and at multiple subcutaneous sites with 750 micrograms of purified monoclonal antibody against Plasmodium falciparum for three times and subsequently boosted by (1) intraperitoneal injection with 750 micrograms of the immunogen, (2) intravenous inoculation with 400 micrograms of the IgG, and (3) intrasplenic immunization with 200 micrograms of the idiotype. With the intraperitoneal boost method, the frequency of hybrids with anti-idiotope activity was 0.3-0.9% with 62.8-85.2% of the seeded wells containing hybrids. In the intravenous boost group, the percentage of hybrids demonstrating anti-idiotope activity increased to 11.0-13.3% with 80.2-97.9% of the hybrid efficiency. When immunized by the intrasplenic boost route, the frequency of anti-idiotope hybrids generated rose to 12.9-16.4% with 82.3-96.6% of the hybrid efficiency. There was no obvious effect of the boost immunizing methods on the generation of rat monoclonal anti-mouse IgG antibodies. These results indicated that the multiple-site immunization followed by intravenous or intrasplenic boost injection was an appropriate immunizing method for the production of monoclonal anti-idiotope antibodies.     

乳腺癌层粘连蛋白的免疫组织化学研究

本研究应用层粘连蛋白（ＬＮ）抗体，对２７例乳腺癌、５例乳腺良性病变进行了免疫组织化学研究。结果发现乳腺良性病变时，ＬＮ以均匀完整的线型阳性反应显示在乳腺导管及小叶基膜处。乳腺癌时，ＬＮ的染色表现为癌细胞胞浆内弥漫状阳性反应。２７例乳腺癌中，癌细胞ＬＮ染色强度不同，伴有转移的乳腺癌ＬＮ染色多数较强，强度在＋＋～的为７／１２（５８．３％）；不伴有转移的病例，ＬＮ染色多数较浅或为阴性，强度在＋＋～＋＋＋的病例为３／１５（２０％）。说明癌细胞内源性ＬＮ染色强弱与肿瘤转移密切相关，内源性ＬＮ的合成可能改变肿瘤细胞的浸润活性。     

竹黄颗粒剂Ⅱ号对应激小鼠皮肤肥大细胞影响的实验研究

目的：阐明竹黄颗粒剂Ⅱ号治疗现的作用机制。方法：应用形态学方法观察竹黄Ⅱ号对应激小鼠皮肤肥大细胞的影响。结果：束缚应激诱导小鼠皮肤肥大细胞脱颗粒，竹黄Ⅱ号抑制了此效应。结论：提示竹黄颗粒剂Ⅱ号可抑制心理应激诱导的皮肤肥大细胞脱颗粒，可能是其治疗银屑病的疗效机制之一。     

单次激发半傅立叶FSE序列MRCP的应用

目的评价单次激发半傅立叶FSE序列MRCP图像质量及诊断价值，分析胆道梗阻性疾病的MRCP影像学表现。方法218例病人行单次激发半傅立叶FSE序列MRCP扫描，然后对图像进行质量评价，根据ERCP及手术结果对照分析胆道梗阻性疾病的MRCP的影像学征象和特点，讨论单次激发半傅立叶FSE序列MRCP在胆道梗阻性疾病中的诊断价值。结果单次激发半傅立叶FSE序列MRCP扫描时间为5～7S，优良图像为82．5％，合格图像为10，6％，差为6．9％。单次激发半傅立叶FSE序列MRCP在胆道梗阻性疾病中，对各类梗阻疾病的定位诊断率为100％，梗阻端形态，胆胰管之间的关系均可显示。病因定性诊断率为95．5%。结论单次激发半傅立叶FSE序列MRCP不受呼吸运动影响，图像优质率高，扫描速度快，可显示各种疾病的胆胰管梗阻改变，对诊断较小的结石及泥沙样结石有较大的价值，诊断较早期胆管癌准确率高，可满足临床诊断的要求。     

A study of tachykinin-immunoreactivity in the cat visual cortex

The localization of tachykinin-immunoreactivity in the cat visual cortex (area 17) was investigated using immunohistochemical methods. Strong laminar specificity was observed, with immunoreactivity highest in layer V, followed by layers I, VI, II and III, and the lowest density in layer IV. Most of the immunoreactive product was localized in neuronal processes. A few immunopositive cell bodies were also present. The immunopositive neurons were non-pyramidal, multipolar, or bipolar in shape, and mostly found in layer V. There were particularly dense immunopositive fibers and varicosities around somata in layer V. These may represent tachykinin-containing presynaptic terminals (boutons). The results provide anatomical evidence that tachykinin may primarily affect layer V neurons in the cat visual cortex.