不同地区妇女产褥期卫生行为研究

目的 了解江苏、陕西和贵州三省妇女产褥期卫生行为和保健的一般情况;比较 不同地区间产褥期各种卫生行为的发生率;了解影响产褥期卫生行为的相关因素。方法 用问卷调查的形式对三者１２个县的２３５２例２岁以下儿童母亲进行入户访问。结果 江苏、陕西、贵州三者产褥期各卫生行为的发和衣次为：洗头２６．４％,３８．８％,１９．８％, 下身（指外阴部,下同）８３．３％,２６．９％,６４．０％,正常活动７６．９％,７     

McAb共刺激PBLs淋巴细胞在培养体系中的状态及超微结构的 …

通过用抗ＣＤ３,ＣＤ２８＋ＣＤ８０ ＭｃＡｂ激活健康人的ＰＢＬｓ,并以ＰＨＡ,ＩＬ－２,ＰＢＬｓ为对照组;对各组不同时间段的淋巴细胞超微结构进行观察。结果提示：ＣＤ３及ＣＤ２８＋ＣＤ８０刺激淋巴细胞增殖外,也能使淋巴细胞活化,细胞表现为胞体增大,细胞器增多,具有粗大的绒毛和突出伪足,并可见单核细胞吞噬活跃。     

造血干细胞移植治疗白血病和淋巴瘤

目的：探讨造血干细胞移植治疗白血病和淋巴瘤的疗效、移植过程中的并发症及其预防和移植后的植活证据及微小残余病灶检测等问题。方法：２例行同胞间异基因骨髓移植（Ａｌｌｏ－ＢＭＴ）、５例行自体外周血干细胞移植（ＡＰＢＳＣＴ）。采用ＣｓＡ＋ＭＴＸ预防ＧＶＨＤ;ＰＧＥ１＋潘生丁预防ＨＶＯＤ;以ＡＰＯＢ、ＳＭ７和Ｄ１Ｓ８０三个位点多态性分析作为植活证据;以ｂｃｒ／ａｂｌ、ＡＭＬ１－ＥＴＯ融合基因或ＩｇＨ基因重排     

香菇多糖与IL-2合用对肺癌浸润淋巴细胞抗瘤活性的影响

目的探讨香菇多糖与IL-2合用对肿瘤浸润淋巴细胞(TIL)抗瘤活性的影响。方法将TIL分别置于含IL-2或IL-2加香菇多糖培养液中培养30d,观察TIL的扩增能力、抗瘤活性的变化。结果IL-2加香菇多糖培养的Til平均扩增倍数和抗瘤活性均明显高于IL-2培养的TIL。IL-2加香菇多糖培养的TIL对自体瘤细胞,K562和Raji细胞的最大杀伤活性分别为67.18±14.73％,71.25±15.86％和66.15±15.07％;而单纯IL-2培养的TIL对各种靶细胞的最大杀伤活性分别为43.81±12.17％,50.83±13.56％和45.41±13.76％。两组相比,差异显著(P＜0.05)。结论香菇多糖与IL-2合用具有促进TIL扩增,增强其抗瘤活性的作用。     

A rubrofusarin gentiobioside isomer from roastedCassia tora

From the roasted seeds ofCassia tora L., a new naphthopyrone glycoside was isolated and characterized as 10-[(β-D-glucopyranosyl-(1→6)-O-β-D-glucopyranosyl)oxyl-5-hydroxy-8-methoxy-2-methyl-4H-naphtho [1,2-b]pyran-4-one(isorubrofusarin gentiobioside). Along with isorubrofusarin gentiobioside, alaternin and adenosine were isolated and identified.     

Chlorogenic acid, an antioxidant principle from the aerial parts ofArtemisia iwayomogi that acts on 1,1-diphenyl-2-picrylhydrazyl radical

The antioxidant activity ofArtemisia iwayomogi was determined by measuring the radical scavenging effect on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical The methanol extract ofA. iwayomogi showed strong antioxidant activity, and thus fractionated with several solvents. The antioxidant activity potential of the individual fraction was in the order of ethyl acetate>n-butanol>water>chloroform>n-hexane fraction. The ethyl acetate andn-butanol soluble fractions exhibiting strong antioxidant activity were further purified by repeated silica gel and Sephadex LH-20 column chromatography. Antioxidant chlorogenic acid was isolated as one of the active principles from then-butanol fraction, together with the inactive components, 1-octacosanol, scopoletin, scopolin, apigenin 7,4′-di-O-methylether luteolin 6,3′-di-O-methylether (jaceosidin), apigenin 7-methylether (genkwanin), 2,4-dihydroxy-6-methoxyacetophenone 4-O-β-D-glucopyranoside and quebrachitol. The antioxidant activity of chlorogenic acid was comparable to that of L-ascorbic acid, which is a well known antioxidant.     

Optimal immobilization of penicillinase for lon-selective electrode

Penicillin sensor was prepared by immobilizing penicillinase (Pcase) on H⁺-selective carboxylated poly (vinyl chloride) (PVC-COOH) membrane or cellulose filter membrane. The immobilization techniques are as follows. Pcase was immobilized with GTH on H⁺-selective PVC-COOH membrane or some amount of BSA was dropped on that membrane. Another method to make immobilization is to mix type I Pcase with GTH and drop on a cellulose filter membrane. According to immobilization techniques, there were some differences in response properties of enzyme electrodes, however, all electrodes responded to Pcase-resistant penicillin derivatives. Pcase immobilized on cellulose filter membrane with H⁺-selective PVC membrane eletrode was more stable and more sensitive to penicillinase-resistant penicillin derivatives than any other immobilization techniques.     

Purification of the NADH reductase component of the steroid 9α-hydroxylase fromMycobacterium fortuitum

The NADH reductase component of the steroid 9α-hydroxylase fromMycobacterium fortuitum was purified to homogeneity. Recovery of the enzyme from the 50≈60% ammonium sulfate saturated fraction was 49%, with a purification factor of 100-fold. The NADH reductase has a relative molecular mass of 60 KDa as determined by SDS-PAGE. The absorption maxima at 410 and 450 nm indicate the presence of iron-sulfur group and flavin. These prosthetic groups seemed to function as redox groups that transfer electrons from NADH to the following protein. The K_M value for NADH as substrate was 68 μM. The NH₂-terminal amino acid sequence of the reductase was determined as Met-Asp-Ala-Ile-Thr-Asn-Val-Pro-Leu-Pro-Ala-Asn-Glu-Pro-Val-His-Asp-Tyr-Ala-Thr. This sequence does not show a homology with the NH₂-terminal sequences reported for the reductase component of other monooxygenases, suggesting that the NADH reductase component of the steroid 9α-hydroxylase system is novel.     

Metabolism of saikosaponin c and naringin by human intestinal bacteria

By human intestinal bacteria, saikosaponin c was transformed to four metabolites, prosaikogenin E1 (E1) prosaikogenin E2 (E2), prosaikogenin E3 (E3) and saikogenin E. Metabolic time course of saikosaponin c was as follows; in early time, saikosaponin c was converted to E1 and E2, and then these were transformed to saikogenin E via E3. Also, this metabolic pathway was similar to the metabolism of saikosaponin c by rat intestinal bacteria.Bacteroides JY-6 andBacteroides YK-4, the bacteria isolated from human intestinal bacteria, could transform saiko-saponin c to E via E1 (or E2) and E3. However, these bacteria were not able to directly transform E1 and E2 to saikogenin E. Naringin was mainly transformed to naringenin by human intestinal bacteria. The minor metabolic pathway transformed naringin to naringenin via prunin. By JY-6 or YK-4, naringin was metabolized to naringenin only via prunin.     

Cytotoxic constituents ofPilea mongolica

Bioassay-guided fractionation of the aerial parts ofPilea mongolica (Urticaceae) afforded two cytotoxic triterpenoids, epi-oleanolic acid (I) and oxo-oleanolic acid (II). The structures of the compounds were confirmed by spectral and synthetic evidences. CompoundI and compoundII exhibited cytotoxicity against cultured human tumor cell lines, A549 (non small cell lung adenocarcinoma), SK-OV-3 (ovarian), SK-MEL-2 (skin melanoma), XF498 (CNS) and HCT15 (colon) with ED(50) values of 3.2 approximately 8.1 mug/ml and 0.7 approximately 6.8 mug/ml, respectively.