核桃仁泥外敷治疗肌肉注射后皮下硬结的疗效观察

采用核桃仁泥外敷治疗１３８例（实验组）肌肉注射后皮下硬结，并与４０例（对照组）采用新鲜土豆片外敷硬结法比较。结果表明：实验组患者治疗１５天后Ⅰ度和Ⅱ度硬结治愈率分别为８１．１３％和４２．２５％，总有效率达９２．０３％，明显优于对照组（Ｐ＜０．００１）。     

Electrophysiological properties of the propafenone-analogue GE 68 (1-[3-(phenylethyl)-2-benzofuryl]-2-(propylamino)-ethanol) in isolated preparations and ventricular myocytes of guinea-pig hearts

GE 68 ((Rac.)-1-[3-(Phenylethyl)-2-benzofuryl]-2-(propylamino)-ethanol hydrochloride) is structurally related to propafenone, and exerts negative inotropic and negative chronotropic effects similar to the parent drug, but lacks any β-adrenoceptor blocking activity contrary to propafenone. Thus, the electrophysiological effects of GE 68 were studied in papillary muscles, left atria, Purkinje fibres, sinoatrial nodes and ventricular myocytes of the guinea-pig heart with the intracellular microelectrode technique and the patch-clamp technique in the cell-attached mode. The decrease of the maximum upstroke velocity (V˙_max) by GE 68 (1 to 10 μM) was use- and frequency-dependent. V˙_max recovered from the use-dependent block with a time constant of 4.1 ± 0.6 s. In papillary muscles and Purkinje fibres action potential duration was shortened, while it was prolonged in left atria and sinoatrial nodes. Half-maximal steady-state inactivation of the sodium channels was shifted to more negative membrane potentials (control: –91.5 ± 0.8 mV, 10 μM GE 68: –97.9 ± 2.5 mV). The peak of the current-voltage relationship and the reversal potential were not changed by GE 68. The amplitude of the unitary current remained unaltered, while open state probability was decreased. The most striking effect of GE 68 was an increase of the number of sweeps without single channel openings (1 μM: 2 fold, 10 μM: 6 fold). GE 68 also caused a decrease of the mean open times, and an increase of the mean closed times in unmodified and pronase-modified sodium channels. Besides the lack of β-adrenoceptor blocking activity, data present a faster recovery from the use-dependent block by GE 68 and a lower affinity to inactivated sodium channels compared to the reference drug propafenone, as well as differences in the effect on single channel kinetics. Received: 25 July 1996 / Accepted: 14 October 1996     

二巯基丙磺酸钠对苯硫丹和多噻烷急性中毒小鼠的保护作用

用二巯基丙磺酸钠对苯硫丹、多噻烷急性染毒小鼠进行保护解救。结果表明：二巯基丙磺酸钠对该两农药急性染毒小鼠具有显著的保护作用（Ｐ＜０．０５）。本实验填补了以二巯基丙磺酸钠作为首选药物治疗沙蚕毒系现有全部品种急性中毒解毒谱的空白。     

神经生长因子对小鼠突触体内Ca^2＋水平的调节作用

观察了多次海马内微注射ＮＧＦ对小鼠突触体内游离钙水平的影响，并在离体情况下观察ＮＧＦ对ＥＧＴＡ和ＣａＣｌ２分别造成突触体内低钙和高钙状态的调节作用。结果如下：（１）在体实验表明，一定剂量的ＮＧＦ可显著降低老年小鼠海马突触体内游离钙水平（Ｐ＜００５）；（２）离体实验表明，当突触体游离钙水平降低时，适当剂量的ＮＧＦ具有升高游离钙水平的作用；而突触体内游离钙水平升高时，则ＮＧＦ有降低游离钙水平的作用。提示ＮＧＦ对游离钙水平的双向调节作用可能是ＮＧＦ改善老年性记忆衰退的作用机制。     

1,6-二磷酸果糖治疗婴幼儿肺炎心衰疗效观察

应用脉冲多普勒超声心动图对３０例使用１，６－二磷酸果糖的肺炎心衰患儿进行心室舒缩功能指标的观测，并以２０例常规治疗的心衰患儿及２０例正常儿为对照组，评价１，６－二磷酸果糖的疗效。结果表明，１，６－二磷酸果糖能明显改善ＰＥＰ、ＰＥＰ／ＥＴ、ＰＥＰ／Ｒ－Ｒ、ＦＶＩ和ＳＶ等心室收缩功能指标及ＰＦＶＥ、Ｅ／Ａ、ＰＦＶＡ等心室舒张功能指标，使心功能恢复正常。１，６－二磷酸果糖对肺炎心衰引起的心肌缺血、缺氧有保护作用。     

内皮素鞘内注射后的脊髓形态学观察

对18只大鼠进行内皮素脊髓鞘内注射,观察及记录大鼠后肢功能状态,并将18只大鼠分为3个不同的时间处死,进行病理形态学观察。结果表明:3组均表现缺血缺氧病理改变。2及4h实验组病变重于30min实验组。脊髓下胸段、腰段病变重于颈段及骶尾段。同时发现,大鼠后肢的功能状态与其脊髓相应的病理形态学变化不呈正比。     

增殖细胞核抗原及nm23在胃癌中的表达及意义

目的 :探讨增殖细胞核抗原 (PCNA)及nm2 3基因在胃癌中的表达及其与生物学行为的关系。方法 :应用免疫组化SP法研究 85例胃癌手术标本中PCNA及nm2 3基因的表达。结果 :在 85例胃癌中PCNA、nm2 3的总阳性表达率分别为 5 2 9% (4 4 / 85例 )和 4 4 .7% (38/ 85例 ) ,PCNA及nm2 3在胃癌中的表达与其淋巴结转移、浸润深度、分化程度有关 (P <0 0 5 ,P <0 0 1 ) ;PCNA与分化程度无关 ,P >0 0 5。结论 :PCNA及nm2 3参与了胃癌的发生、发展、浸润及转移     

免疫球蛋白联合鞘内注射激素治疗重症格林-巴利综合征

目的观察免疫球蛋白联合鞘内注射激素治疗重症格林-巴利综合征的疗效。方法应用Hughes量表评价疗效。结果治疗组起效时间明显短于对照组,治疗组Hughes临床分级评分改善明显优于对照组。结论免疫球蛋白联合鞘内注射激素治疗重症格林-巴利综合征可缩短病程、缓解急性期症状。     

6种中药制剂治疗急性脑梗死的成本-效果分析

目的：运用药物经济学的方法对在我院应用的6种中药注射液进行成本-效果分析。方法：271例急性脑梗死患者依据药物治疗方案不同分为6组，即血塞通组、舒血宁组、苦碟子组、疏血通组、川芎嗪组、丹红组，分别观察疗效，并运用药物经济学的方法进行成本-效果分析。结果：疏血通组的成本为3 419.90元，总有效率最高（91.84%），6组间增量成本-效果最低。因此疏血通组是较为合理、经济的方案。     

喜炎平注射液联合维生素K3治疗小儿秋季腹泻的疗效观察

目的观察喜炎平与维生素K3联合治疗小儿秋季腹泻的疗效.方法将89例秋季腹泻患儿随机分为2组.治疗组采用喜炎平与维生素K3联合治疗,对照组则采用利巴韦林治疗,疗程5d.结果治疗组的总有效率为93.3%,显著优于对照组的65.9%(X2=10.37,P＜0.01).结论喜炎平与维生素K3联合治疗小儿秋季腹泻值得进一步推广.