TRP超家族与肾脏

TRP(Transient receptor potentical)家族是非选择性阳离子通道家族，近来发现其与肾脏关系密切，如调节肾小管离子转运，肾脏微循环等。TRP通道异常可导致遗传性局灶节段硬化性肾病（FSGS），常染色体显性遗传多囊肾(ADPKD)，低镁血症继发低钙血症(HSH)等，对TRP通道的进一步研究将有助于临床肾脏病的防治。     

Regulation of organic cation transport

Transport of organic cations (OC) is important for the recycling of endogenous OC and also a necessary step for detoxification of exogenous OC in the body. Even though the identification and characterisation of numerous OC transporters in recent years has allowed the elucidation of molecular mechanisms underlying OC transport, elucidation of the regulation of this transport is just beginning. This review summarises the general properties of OC transport and then analyses the literature on the regulation of these processes. Studies on short- and long-term regulation of OC transport are considered separately. Important aspects of short-term regulation have been clarified and the regulatory pathways of several OC transporters have been characterised. Short-term regulation appears to be transporter subtype-, tissue- and species-dependent and to involve transporter phosphorylation. Transporter phosphorylation may alter the affinity for substrates or/and expression on the plasma membrane. Even though several studies have shown long-term regulation of OC transport, the pathophysiological meaning of these changes are not well understood. In this case, regulation seems to be subtype-, tissue- and gender-specific. Further research is necessary to clarify this important issue of regulation of OC transport.     

Effects of diadenosine polyphosphates,ATP and angiotensin II on membrane voltage and membrane conductances of rat mesangial cells

Diadenosine polyphosphates have been shown to influence renal perfusion pressure. As mesangial cells may contribute to these effects we investigated the effects of diadenosine triphosphate (Ap₃A), diadenosine tetraphosphate (Ap₄A), diadenosine pentaphosphate (Ap₅A) and diadenosine hexaphosphate (Ap₆A) on membrane voltage (V _m) and membrane conductance (g _m) in mesangial cells (MC) of normotensive Wistar-Kyoto (WKY) and spontaneously hypertensive (SHR) rats in primary and long-term culture. We applied the patch-clamp technique in the fast-whole-cell configuration to measure V _m and g _m. To compare the effects of diadenosine polyphosphates with hitherto known agonists we also tested adenosine 5-triphosphate (ATP) and angiotensin II (Ang II). As there was no significant difference in the V _m values in MC of WKY (–42±1 mV, n=70) and SHR rats (–45±2 mV, n=99) as well as in the agonist-induced changes of V _m, all data were pooled. The V _m of all the cells was –44±1 mV (n=169) and g _m was 15.9±1.8 nS (n=141). Ion-exchange experiments showed the presence of a K⁺ and a non-selective cation conductance in resting MC whereas a Cl^– conductance or a Na⁺selective conductance could not be observed. Ap₃A, Ap₄A, Ap₅A, AP₆A and ATP each at a concentration of 5 mol/l, led to a significant depolarization of V _m by 5±2 mV (n=14), 7±1 mV (n=25), 3±1 mV (n=23), 2±1 mV (n=16), and 14±2 mV (n=23), respectively. For Ap₄A, the most potent diadenosine polyphosphate, we determined the half-maximally effective concentration (EC ₅₀) as 6 mol/l (n=5–25), for ATP as 2 mol/l (n=9–37), and for Ang II as 8 nmol/l (n=6–18). Ap₄A 100 mol/l increased g _m significantly by 55±20% (n=16), 100 mol/l ATP by 135±60% (n=18). The diadenosine polyphosphates examined were able to depolarize V _m (Ang II >ATP> Ap₄A>Ap₃A>Ap₅A>Ap₆A) by activation of a Cl^– conductance and a non-selective cation conductance, as do ATP or Ang II.     

1—甲基—4—苯基吡啶啶离子诱发大鼠小脑颗粒细胞凋亡

目的 建立1－甲基－4－苯基吡啶离子（1－methy1-4-phenyl pyridinium ion,MPP^ )诱导的大鼠小脑颗粒细胞凋亡模型。方法 MPP^ 处理大鼠小脑颗粒细胞,分别用甲基绿－派诺宁染色,DNA凝胶电泳,流式细胞术进行检测。结果 浓度为50μmol/L MPP^ 使小脑颗粒细胞发生凋亡。结论 以MPP^ 为诱导剂建立的大鼠小脑颗粒细胞凋亡模型,可用于研究和帕金森病（PD）有关的细胞凋亡的调控机制和筛选抗PD药物。     

硬质PVC／ACR共混体系的增韧机理研究

通过TEM、SEM等方法研究了不同结构丙烯酸酯类抗冲改性剂（ACR）对聚氯乙烯（PVC／ACR共混体系形态结构的影响,对ACR增韧硬质PVC的机理作了探讨,当PVC中含有8phr以上完善核壳结构的ACR时,在共混体系能形成网络结构,这一结构在受冲击时产生多重银纹,并实现银纹的纯化,在PVC／ACR共混体系的增韧机理中占主导地位,同时,ACR诱发PVC产生剪切形变也是提高其增韧效果的因素。     

Studies an morphological typing of argyrophilic nucleolar organizer regions

Morphological typing of argyrophilic nucleolar organizer regions (AgNOR) in 300 caws of malignant tumors and 140 cams of benign lesions was analyzed and five morphological types of ApNOR were described in detail. In malignant tumors, the diffuse type (78%) was the most frequently seen, and in benign lesions, the nucleolar type (92.85%); the difference was thus highly significant (P < 0.001). The intranucleolar and aggregate types were not observed in benign lesions. There was no obvious difference in the proportion of the mixed type in benign and malignant lesions (P > 0.05). The relationship between grade of malignancy and morphological typing of AgNOR and its clinical significance are discussed.     

炮口冲击波引起的山羊病理形态学改变

目的 探讨炮口冲击波对山羊的病理形态学改变。方法 用１２５ｍｍ火炮单发发射穿甲弹,进行大体形态学,光镜和电镜观察。结果 肺是炮口冲击波作用最敏感的内脏器官,大体解剖主要表现为不同程度的肺出血;光镜观察可见肺泡出血、水肿,肺泡明显扩张,肺不张和炎细胞浸润;电镜观察可见肺泡上皮肿胀、变性、微绒毛减少、肺泡隔增生纤维化。上呼吸道和胃肠道对炮口冲击波也较为敏感,主要表现为不同程度的帮浆膜下出血。结论 炮口     

Expression of the extraneuronal monoamine transporter (uptake2) in human glioma cells

Tritiated methylphenylpyridinium ([³H]MPP⁺), a substrate of the neuronal and extraneuronal noradrenaline transporter (uptake₁ and uptake₂, respectively) and of the organic cation transporter (OCT1), was used to characterize the amine transport system of the established human glioma cell line SK-MG-1.Uptake of [³H]MPP⁺ (25 nM) into SK-MG-1 cells increased linearly with time for up to 15 min. Selective uptake₁ inhibitors (e.g. (+)oxaprotiline) or omission of Na⁺ or Cl^– ions did not affect [³H]MPP⁺ uptake, whereas uptake₂ inhibitors such as O-methyl-isoprenaline (OMI) or corticosterone as well as depolarizing concentrations of K⁺ or Ba²⁺ strongly reduced [³H]MPP⁺ uptake. Initial rates of OMI(100 M)-sensitive [³H]MPP⁺ uptake were saturable, with a K_m of about 17 M and a maximal rate of about 50 pmol/ (min × mg protein). IC₅₀ (or K_i) values for inhibition of [³H]MPP⁺ uptake by substrates and inhibitors of uptake₂ or OCTI were highly significantly correlated with published IC₅₀ values for inhibition of uptake₂ but not with corresponding values for inhibition of OCT1.The results presented here clearly demonstrate that human glioma cells express an uptake₂ transporter. Thus, glial cells in the human central nervous system endowed with this transporter are likely to contribute to the inactivation of neuronally released noradrenaline.     

Interleukin-1 receptor antagonist in newborn babies and pregnant women

We have used patch-clamp techniques to study the effect of the sulfhydryl group oxidizing agents mercury and thimerosal on calcium-activated nonselective cation channels from brown adipose tissue. 100 nmol/l mercury and 50 mol/l thimerosal induced a complete block. Blockade could be reversed by reduction of the mercaptide by dithiotreitol (DTT). Mercury was found to be the most potent blocker (IC₅₀-value 21×10^–9 mol/l), whereas thimerosal (IC₅₀-value 1.5×10^–6 mol/l) was as effective as 3,5-dichlorodiphenylamine-2-carboxylic acid (DCDPC). The DCDPC effect, however, could not be reversed by DTT, indicating different blocking mechanisms. It is concluded that SH-groups are involved in gating of the calcium-activated nonselective channel.     

怀槐愈伤组织形成与异黄酮积累

目的 :考察怀槐愈伤组织形成与总异黄酮积累的关系。方法 :不同培养基诱导怀槐子叶和下胚轴产生愈伤组织 ,紫外分光光度术测定愈伤组织中总异黄酮并含量。结果 :NAA /BA及含 2 ,4-D组合有利子叶愈伤组织的诱导 ;MS ,N6 ,B5培养基适宜子叶形成愈伤组织 ,而SH较适宜下胚轴产生愈伤组织。愈伤组织具有异黄酮合成能力 ,含有NAA激素组合诱导的子叶愈伤组织总异黄酮含量较高 ,而 2 ,4-D/BA组合诱导的下胚轴愈伤组织总异黄酮含量较高 ,高浓度 2 ,4-D/KT组合抑制子叶和下胚轴愈伤组织积累异黄酮。愈伤组织根据发育的形态特征可分为 4种类型 ,以黄色、疏松、颗粒状的Ⅱ型愈伤组织中总异黄酮含量最高。结论 :培养基与激素组合影响愈伤组织的形成及发育形态特征 ,并反映在愈伤组织异黄酮合成差异上 ,获得的黄色、疏松颗粒状愈伤组织为后续的细胞液体悬浮培养及异黄酮合成代谢的调控研究奠定了基础。