Parvalbumin-immunoreactive neurons in the cerebral cortex of the lizardPodarcis hispanica

An antibody against the calcium binding protein parvalbumin selectively labels a set of neurons in the cerebral cortex of lizards. Golgi-like immunostained bipolar, multipolar and pyramid-like neurons appear mainly located in the inner plexiform layers. Parvalbumin-immunoreactive (PARV-IR) puncta are concentrated in the cell layer of the dorsal and dorsomedial cortices showing a basket-like distribution. The morphology and distribution of PARV-IR neurons and puncta overlap GABA-immunostaining in the cerebral cortex of lizards. Thus, it is likely that PARV-IR neurons are a subset of the cortical GABAergic neurons of lizards.     

Comparison of assays for determination of peptide content for lyophilized thymalfasin*

Abstract: Precise determination of the peptide content in drug substance samples depends highly upon the particular peptide compound and methodology used. Four independent methods were evaluated and compared to determine which would produce the best experimental precision for analysis of thymalfasin (thymosin α‐1). Four different methods were evaluated including elemental analysis (CHN), quantitative amino acid analysis (AAA), high‐performance liquid chromatography (HPLC), and Kjeldahl. This study demonstrates that the AAA method is highly variable in one laboratory while quite precise in another laboratory. Similarly, HPLC results depended on the laboratory conducting the study with more precise values obtained under cGMP. On the contrary, the CHN method yielded highly precise [i.e. <2% coefficient of variation (CV)] values. As precise knowledge of protein content is fundamental for the compounding of final pharmaceutical product of a specific potency, the CHN analysis is recommended for peptide content determination of the drug substance thymalfasin.     

超声引导下犬肝注射醋酸高渗氯化钠混合液对射频消融毁损体积的影响

目的探讨超声引导下活体犬肝注射不同剂量的醋酸高渗氯化钠液(acetic acid hypertonic saline solution,AHS)后行射频消融(RFA),观察犬肝一次性毁损体积的变化。方法使用LDRF-120S多极RFA系统联合AHS对活体犬肝行RFA。健康成年杂种犬30只,随机分为5组(n=6)。A组:注射2ml AHS后立即行RFA;B组:注射2ml AHS后延时5min行RFA;C组:注射4ml AHS后立即行RFA;D组:注射4ml AHS后延时5min行RFA;E组:注射6ml AHS后立即行RFA。结果5组间平均起始阻抗差异无统计学意义(P>0.05);5组间平均消融时间差异有统计学意义(F=83.831,P<0.001),LSD-t检验分析各组间两两比较差异有统计学意义(P<0.001),在观察范围内E组平均消融时间最长;5组间平均毁损直径差异有统计学意义(F=53.488,P<0.001),在观察范围内E组平均毁损直径最大,LSD-t检验分析除D与E组间差异无统计学意义(P>0.05)外,其余各组间两两比较差异有统计学意义(P<0.001);网状纤维染色显示凝固坏死区及其邻近的正常肝组织均可见血管内血栓形成;E组在AHS注射过程中出现不同程度的外溢;A、B、C及D组14d内无动物死亡,E组死亡4只。结论活体犬肝局部注射AHS4ml后延时5min行RFA即可达到较理想的毁损体积。     

腹外侧视前区GABA能神经元对大鼠睡眠-觉醒周期的影响

目的 研究腹外侧视前区(VLPO）γ-氨基丁酸(GABA)能神经元对大鼠睡眠—觉醒周期的影响。方法 采用脑立体定位、核团微量注射和多导睡眠描记技术。结果 VLPO双侧分别微量注射GABA合成关键酶(谷氨酸脱羧酶，GAD)抑制剂3-巯基丙酸(3-MP，5μg，0．1μl)，与对照组相比，注射后当日对大鼠睡眠—觉醒周期无影响；注射后第1天大鼠睡眠量减少，觉醒时间增加；第2、3天恢复正常。结论 GABA能神经元在VLPO参与大鼠睡眠—觉醒周期调节且有促睡眠作用。     

高原红细胞增多症患者血清尿酸水平分析

目的研究高原红细胞增多症患者(HAPC)血清尿酸(uric ac id,UA)的水平及其临床意义。方法选择HAPC患者78例,采集患者静脉血检测血清中尿酸的含量,并与80例高原健康人作对照研究。结果HAPC组血清尿酸的含量显著高于正常对照组(P<0.05)。结论在治疗高原红细胞增多症时应关注患者血尿酸水平。     

MR频谱检测乳酸的脉冲序列优化研究

目的通过改变一系列脉冲序列参数，以利于乳酸的最佳检测与定量分析。方法制作含乳酸玻璃模型。改变一系列的MR脉冲序列参数，应用点解析频谱序列(point resolved spectroscopy，PRESS)和激励回波序列(stimulated echo acquisition，STEAM)获得乳酸模型的相应频谱。另外，对12例脑病变患者和2例健康志愿者进行磁共振频谱检查，测量出每个波峰的峰高，并绘出序列变化曲线图。结果STEAM各波峰的峰向与PRESS序列一致，但STEAM各峰高均低于同等条件的PRESS峰。随着TE时间的延长，用乳酸模型测出的乳酸峰的峰高一序列曲线图呈波浪状变化，正向双峰在TE=26、270ms时共振波幅达到最大绝对值，负向双峰在TE=135～160ms之间达到最大绝对值。脑病变患者和健康志愿者的扫描结果表明，乳酸峰在优化的序列高于非优化的序列。结论优化的脉冲序列更有利于乳酸的检测与定量分析。     

市售三厂家18种复方氨基酸注射液的质量评价

目的对市售3厂家(A、B和E)共9批18种复方氨基酸注射液进行质量比较。方法参考国内外同类产品质量标准,从澄明度、透光率、性状、pH值、不溶性微粒、抗氧剂量、细菌内毒素和含量等方面进行比较。结果外观均为无色澄明液体,430nm波长处透光率均大于99%,pH在5.42～6.61间;A、B、E3厂不溶性微粒≥10、≥25μm的粒子数分别为1.41、0.32,0.83、0.21和1.55、0.56个/ml;抗氧剂的量分别为<33、近330和>500mg/L;细菌内毒素检查与含量测定符合中国药典及国家标准要求。结论不同厂家的产品质量确实存在一定的差异。     

透明质酸对BMP-2转染的羊BMSCs增殖、分化的影响

目的观察透明质酸（HA）对携带人骨形态发生蛋白-2的腺病毒（Adv-BMP-2）转染的羊骨髓基质干细胞（BMSCs）体外增殖、分化的影响。方法将羊骨髓体外分离、扩增BMSCs,分成5组：转染Adv-BMP-2的BMSCs＋HA组（Ⅰ组）,转染Adv-BMP-2的BMSCs组（2组）,BMSCs＋HA组（3组）,BMSCs组（4组）,转染携带β半乳糖苷酶的腺病毒（Adv-β-gal）的BMSCs组（5组）。采用细胞计数、绘制细胞生长曲线和流式细胞分析观测细胞增殖;采用碱性磷酸酶（ALP）检测以及RT-PCR检测Ⅰ型胶原（Col-Ⅰ）、骨连接素（ON）和骨涎蛋白（BSP）的mRNA表达。结果①细胞增殖：3 d后各组细胞增殖无显著差异,1周后第1组和第3组的细胞增殖明显高于其他组。②ALP活性：3 d后第3组ALP活性明显低于第4、5组,而第1、2组则显著高于第4、5组;7 d后前3组ALP活性较后两组均显著增加,而第1、2组ALP活性增加更为显著。③Col-Ⅰ、ON和BSP的mRNA表达：3 d和7 d后前3组较后两组均有不同程度的增多。结论HA与BMSCs体外复合培养后可促进BMSCs的增殖、增加ALP的活性以及Col-Ⅰ、ON和BSP基因的表达。     

Quantitative analysis of urinary glycine conjugates by high performance liquid chromatography: excretion of hippuric acid and methylhippuric acids in the urine of subjects exposed to vapours of toluene and xylenes

Summary A new method for the direct determination of hippuric acid (HA) and o-, m- and p-methylhippuric acids (MHAs) in the urine, metabolites of toluene and o-, m- and p-xylenes by high performance liquid chromatography (HPLC) is described. A stainless-steel column packed with silica gel having dinitrophenyl residue and a mixed solution of methanol/water/acetic acid (80/20/0.2) containing tetra-n-butylammonium bromide (0.2% w/v) as mobile phase was used. Concentrations of HA and MHAs were estimated from their peak height at a wave length of 225 nm. Urine can be analyzed directly without solvent extraction or pretreatment to obtain complete separation of HA and o-, m- and p-MHAs. Urine samples from male workers exposed to toluene or xylenes were analyzed for HA or MHAs. The urinary levels of HA and MHAs increased by exposure to toluene and xylenes in proportion to the environmental concentrations of the solvents, although there is a considerable variation in metabolite concentrations. The slope of regression line between toluene and HA and that between m-xylene and m-MHA were similar. The urinary concentrations of HA and MHAs corresponding to 100 ppm (TLV) of toluene was 2.35 g/g creatinine and that of m-MHA corresponding to 100 ppm (TLV) of m-xylene was 2.05 g/g creatinine. The warning levels of the urinary metabolite concentrations of a group of workers and that of an individual worker corresponding to TLV of organic solvent concentration is discussed.     

涂剂中苯甲酸和硝酸咪康唑含量的薄层色谱扫描测定法

本文建立了苯甲酸咪康唑剂涂剂的薄层色谱扫描测定法。点样后的硅胶GF_(254)薄层板,经正已烷—氯仿—甲醇—二乙胺(42:21:13:5)混合溶剂上行展开后,反射锯齿扫描测定,λ=220um,SX=3,外标一点法定量计算。苯甲酸和硝酸咪康唑测定的线性范围分别2～6μg和12～36μg,方法准确、简便。