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81.
目的:观察和总结瘤内注射治疗颌面部血管瘤的疗效。方法:采用醋酸曲安奈德注射液加平阳霉素局部注射治疗婴幼儿颌面部血管瘤,如一次注射治疗未愈的,间隔4~6周重复给药,4次为一个疗程,醋酸曲安奈德总量不超过100mg,平阳霉素总量不超过40mg;观察肿瘤消退情况。结果:84例患儿,经1年随访,治愈率(90.4%),显效率(7.1%),无效率(2.4%)。结论:本方法疗效可靠、副作用小、外观较满意,适合婴幼儿颌面部血管瘤的治疗。 相似文献
82.
Jeffrey F. Waring Rita Ciurlionis Robert A. Jolly Matthew Heindel Gerry Gagne Jane A. Fagerland Roger G. Ulrich 《Toxicology in vitro》2003,17(5-6):693-701
In vitro human hepatocyte cultures are a key tool in the investigation of xenobiotic toxicity and metabolism. In most in vitro hepatocyte studies, the cells are allowed to adhere to an extracellular matrix, such as collagen. Unfortunately, the ability of freshly isolated hepatocytes to adhere to collagen varies from donor to donor. We used microarray analysis to determine what gene expression differences exist between hepatocytes in suspension and hepatocytes attached to collagen. Results from different donors showed a considerable difference in gene expression patterns between the two hepatocyte populations. In addition, we also compared the gene expression profiles of hepatocytes in culture with liver tissue. The results showed that both hepatocytes in suspension and hepatocytes attached to collagen display significant gene expression differences compared with liver tissue. Finally, we show that both populations of hepatocytes are responsive to dexamethasone and regulate some of the same genes. Overall, our results suggest that either significant gene expression changes occur in isolated hepatocytes or that suspended and attached cells represent different populations of hepatocytes found in intact livers. 相似文献
83.
40例肺癌切除术病人,随机分为对照(S)组和地塞米松(S-D)组,采用氯胺酮-安氟醚静吸复合麻醉,对血清中过氧化脂质、胰岛素和皮质醇进行了初步观察。结果表明,血清过氧化脂质S-D组于手术毕显著低于S组(P〈0.05);血清胰岛素两组间没有统计学差异;血清皮质醇S-D组于气管插管后显著高于S组(P〈0.05)。作者认为肺癌切除术病人术前给地塞米松可有效地降低血清中过氧化脂质含量,利于维护脏器功能。 相似文献
84.
Two experiments were performed to investigate the relationship between the expression of sodium appetite and the appearance of Fos-like immunoreactivity (Fos-IR) in the brain of rats. In the first experiment, rats were depleted of sodium by treatment with furosemide 24 h prior to sacrifice and without access to either food or sodium solution. Some rats had access to distilled water, and others had no fluids available during the 24 h. All of the furosemide-treated rats showed Fos-IR in both the subfornical organ (SFO) and around the organum vasculosum laminae terminalis (OVLT). Rats with access to distilled water during the depletion period showed no Fos-IR in the supraoptic (SON) or paraventricular hypothalamic nuclei (PVN) and, in parallel behavioral studies, comparably-treated rats consumed only 0.3 M NaCl solution at the end of the 24 h. In rats that had no fluids during the deprivation period, only about one half showed Fos-IR in SON and PVN and, in parallel behavioral studies, comparably treated rats consumed both water and 0.3 M NaCI solution at the end of 24 h. In a second experiment, cerebroventricular administration of renin stimulated short latency intake of 0.3 M NaCI and water. The relative intakes of water and NaCl were comparable at a low dose of renin, but intake of water exceeded that of NaCl after higher doses. Renin induced Fos-IR in SFO, MnPO, peri-OVLT region, SON and PVN. Both Fos-IR and fluid intake were antagonized by administration of losartan, an angiotensin 11 type 1 receptor antagonist. Thus, only the circumventricular organs of the lamina terminalis showed Fos-IR during each natriorexigenic regimen in these studies. These data support the view that Ang 11 of both central and peripheral origin activates the SFO and/or peri-OVLT region and contributes to sodium appetite. 相似文献
85.
正常血钾型周期性麻痹SCN4A基因新突变的检测 总被引:7,自引:1,他引:6
目的 报道正常血钾型周期性麻痹 (normoPP)一家系的临床特点 ,并筛查SCN4A基因以期发现有义突变。方法 提取知情同意的患者及部分家属外周血基因组DNA ,应用变性高效液相色谱分析 (DHPLC)技术筛查患者SCN4A基因全部 2 4个外显子 ,对发现异常者进行测序分析。结果先证者常规实验室检查未见异常 ,发作期肌酸激酶 (CK) 112 6U/L(正常值 <2 0 0U/L) ,肌电图正常。发作间期行肌肉活检未见显著异常。基因研究发现先证者及其父亲 (患者 )SCN4A基因发生同一新突变G2 10 1A ,并引起氨基酸序列改变Arg6 75Gln。该突变不同于目前发现的明确导致高钾型周期性麻痹(hyperPP)的突变 ,也不同于已知的SCN4A基因所有突变。结论 normoPP患者存在一新突变Arg6 75Gln ,该突变可能与疾病相关。 相似文献
86.
背根神经节Nav1.8磷酸化在大鼠糖尿病痛性周围神经病变中的作用 总被引:2,自引:0,他引:2
目的 本研究采用射频热凝毁损腰交感神经节,探讨背根神经节(DRG)Nav1.8磷酸化在大鼠糖尿病痛性周围神经病变中的作用。方法 采用腹腔注射链尿佐菌素诱导糖尿病痛性周围神经病变大鼠模型,取造模成功的大鼠20只,随机分为糖尿病对照组(D组)及交感神经节射频热凝组(R组),每组10只,另取10只同月龄大鼠为正常对照组(C组)。R组大鼠在X光机介导下行右侧L3,4椎旁腰交感神经节射频热凝毁损。分别于射频热凝前、射频热凝后1、2周时,采用von Frey纤维丝测定大鼠右侧后爪对机械性刺激缩足反应的阈值(PWT);射频热凝后2周,采用Western-blotting方法测定DRG细胞Nav1.8蛋白和苏氨酸磷酸化Nav1.8蛋白表达,并采用透射电镜观察大鼠腓肠神经超微病理结构。结果 与C组比较,射频热凝前D组和R组PWT降低(P<0.01)。射频热凝后1~2周,R组较D组PWT升高,但仍较C组降低(P<0.05)。C组髓鞘排列均匀,轴突内可见形态正常的线粒体;D组脱髓鞘明显,髓鞘板层排列紊乱、断裂、肿胀;R组脱髓鞘程度明显减轻,髓鞘板层局部排列紊乱、空泡形成。与C组比较,D组和R组Nav1.8蛋白表达降低(P<0.05),而苏氨酸磷酸化Nav1.8蛋白表达增高(P<0.01);R组苏氨酸磷酸化Nav1.8蛋白表达低于D组(P<0.05)。结论 DRG细胞Nav1.8的磷酸化可能是糖尿病痛性周围神经病变大鼠痛觉过敏形成的机制之一。 相似文献
87.
目的探讨硬膜外腔注射生理盐水对剖宫产术患者腰麻效果的影响。方法择期行子宫下段剖宫产术患者60例,年龄24~30岁,体重59~73 kg,随机分为2组,每组30例,A组蛛网膜下腔注射规定剂量的0.75%布比卡因后硬膜外腔注射生理盐水5 ml;B组蛛网膜下腔注射0.75%布比卡因。按序贯法进行试验,设定布比卡因的起始剂量为9 mg,剂量梯度为1.5 mg,若上一例有效,则下一例递减一个剂量梯度,若无效则下一例递增一个剂量梯度,蛛网膜下腔阻滞有效的标准为注射布比卡因后20 min内阻滞上平面达T5。采用概率单位法计算ED50。结果A组布比卡因的ED50(5.8 mg)低于B组(8.1 mg),两组比值为0.72,95%置信区间为0.27~0.98,区间范围不包括1,差异有统计学意义(P〈0.05)。结论硬膜外腔注射生理盐水可增强剖宫产术患者腰麻的效果。 相似文献
88.
Ion channel expression by white matter glia: I. Type 2 astrocytes and oligodendrocytes 总被引:12,自引:0,他引:12
White matter is a compact structure consisting primarily of neuronal axons and glial cells. As in other parts of the nervous system, the function of glial cells in white matter is poorly understood. We have explored the electrophysiological properties of two types of glial cells found predominantly in white matter: type 2 astrocytes and oligodendrocytes. Whole-cells and single-channel patch-clamp techniques were used to study these cell types in postnatal rat optic nerve cultures prepared according to the procedures of Raff et al. (Nature, 303:390-396, 1983b). Type 2 astrocytes in culture exhibit a "neuronal" channel phenotype, expressing at least six distinct ion channel types. With whole-cell recording we observed three inward currents: a voltage-sensitive sodium current qualitatively similar to that found in neurons and both transient and sustained calcium currents. In addition, type 2 astrocytes had two components of outward current: a delayed potassium current which activated at 0 mV and an inactivating calcium-dependent potassium current which activated at -30 mV. Type 2 astrocytes in culture could be induced to fire single regenerative potentials in response to injections of depolarizing current. Single-channel recording demonstrated the presence of an outwardly rectifying chloride channel in both type 2 astrocytes and oligodendrocytes, but this channel could only be observed in excised patches. Oligodendrocytes expressed only one other current: an inwardly rectifying potassium current that is mediated by 30- and 120-pS channels. Because these channels preferentially conduct potassium from outside to inside the cell, and because they are open at the resting potential of the cell, they would be appropriate for removing potassium from the extracellular space; thus it is proposed that oligodendrocytes, besides myelinating axons, play an important role in potassium regulation in white matter. The conductances present in oligodendrocytes suggest a "modulated Boyle and Conway mechanism" of potassium accumulation. 相似文献
89.
Miwa Baba Ryozo Oishi Kiyomi Saeki 《Naunyn-Schmiedeberg's archives of pharmacology》1988,337(4):423-428
Summary The effects of opioids on the permeability of the blood-brain barrier (BBB) were examined in mice with sodium fluorescein as an indicator of the permeability. The brain was perfused with saline 30 min after injection of sodium fluorescein (40 mg/kg, i. v.) and examined by fluorometry. Morphine hydrochloride (0.3–10 mg/kg, s. c.) markedly increased the brain level of sodium fluorescein dose-dependently without influencing the plasma level, when administered 20 min before sodium fluorescein injection. Intracerebroventricularly (i. c. v.) injected morphine hydrochloride (0.5 and 1.0 Erg) increased the brain sodium fluorescein level. Buprenorphine (0.1 and 0.5 mg/kg, s. c.) was also effective. However, pentazocine, ethylketazocine, U-50488H and SKF-10047 had no significant influence. The i.c.v. administration of [D-Ala2, McPhe4, Gly(ol)5]enkephalin (0.1 g) and [D-Ala2, D-Leu5]enkephalin (0.5 g) but not of [D-Thr2, Leu5]enkephalin-Thr increased the brain level of sodium fluorescein significantly. A small dose of naloxone (i. p.) significantly inhibited the effects of morphine, buprenorphine, [D-Ala2, McPhe4, Gly(ol)5]enkephalin and [D-Ala3, D-Leu5]enkephalin. ICI-174864 co-administered i. c. v. with [D-Ala2, D-Leu5]enkephalin was ineffective in antagonizing the effect of the latter. These findings suggest that the stimulation of µ opioid receptors results in an increase in BBB permeability to sodium fluorescein.
Send offprint requests to K. Saeki 相似文献
90.
Francisco Alvarado Edith Brot-Laroche Manuel L'Herminier Heini Murer Gertrude Stange 《Pflügers Archiv : European journal of physiology》1979,382(1):35-41
Harmaline inhibition of sodium uptake and of sodium-dependentd-glucose transport was investigated using brush-border membrane vesicles from frozen rabbit jejunum. Under sodium-gradient conditions, initiald-glucose uptake (20 s) was inhibited by harmaline at concentrations above 0.5 mM, but at lower harmaline concentrationsd-glucose uptake was stimulated by 10–15%. When a similar potassium gradient was used, harmaline had no effect. At concentrations upt to 2 mM, harmaline did not alter the equilibrium uptake ofd-glucose ord-mannitol. After pre-equlibration with sodium (25 mM),d-glucose uptake was inhibited at harmaline concentrations ranging from 0.1 to 2 mM. Sodium (10 mM) uptake was also inhibited by harmaline. Increasing the sodium concentration reduced the inhibitory effect of harmaline on tracer sodium uptake as well as on sodium-dependentd-glucose uptake. Similar to phlorizin, harmaline (1 mM) was able to prevent glucose-induced sodium influx across the brush-border membrane.Sodium uptake into brush-border membrane vesicles seems to be inhibited at lower harmaline concentrations than sodium-dependentd-glucose uptake. At high (2 mM) inhibitor concentrations, however, sodium-dependent glucose uptake is more strongly inhibited than sodium uptake. These results suggest that harmaline inhibits both sodium and sodium-dependent transport across intestinal brush-border membranes by interacting with specific sodium-binding sites. 相似文献