Presenza di enteramina o di una sostanza enteraminosimile negli estratti gastrointestinali e splenici dei pesci e negli estratti gastroenterici delle Ascidie

Summary It was possible to demonstrate, by means of chemical and biological reactions, the presence of enteramine or of an enteramine-like substance in gastro-intestinal extracts of twoAscidi, Tethium plicatum andCiona intestinalis.The same substance was also found in gastric and still more in intestinal extracts ofSelacia, but seems not to be present in the spleen ofSelacia nor in the alimentary canal ofTeleostea.     

水合物地层低温钻井液对井底岩石表层强度影响

由于天然气水合物仅在高压低温条件下稳定存在,为了保持水合物稳定,在钻井过程中宜采用低温钻井液,而在低温条件下钻井液能否对井底岩石表层起到软化作用,对于提高机械钻速具有重要意义。在分析钻井液对井底岩石表层软化作用机制的基础上,较系统地建立低温钻井液软化井底岩石表层定量评价方法,以清水为对比浆液,通过试验将6种水合物地层模拟钻井液(分别含有质量分数为0.1%的表面活性剂和有机盐处理剂)在低温条件下对薄片砂岩试样的软化效果进行对比。结果表明:相比于两种有机盐处理剂,含表面活性剂的4种模拟钻井液在低温条件下对岩样软化效果更好,有利于提高岩石破碎效率和机械钻速;4种含表面活性剂钻井液中,含十二烷基硫酸钠(SDS)钻井液对岩样的软化效果最好。     

Sex-dependence in triglyceride metabolism in response to dietary carbohydrates.

In humans, as well as in mice, fed on high carbohydrate diets, there was a significant sex difference in the plasma tirglycerides in that males had higher levels than females. This was mainly due to the difference in their removal rate of circulating triglycerides in the animals of both sexes. In mice, males had higher levels of liver triglycerides as well as higher rate of incorporation of U- 14C-glucose into liver triglycerides when compared to females.     

Actin-based motility of vaccinia virus mimics receptor tyrosine kinase signalling.

Studies of the actin-based motility of the intracellular pathogens Listeria monocytogenes and Shigella flexneri have provided important insight into the events occurring at the leading edges of motile cells. Like the bacteria Listeria and Shigella, vaccinia virus, a relative of the causative agent of smallpox, uses actin-based motility to spread between cells. In contrast to Listeria or Shigella, the actin-based motility of vaccinia is dependent on an unknown phosphotyrosine protein, but the underlying mechanism remains obscure. Here we show that phosphorylation of tyrosine 112 in the viral protein A36R by Src-family kinases is essential for the actin-based motility of vaccinia. Tyrosine phosphorylation of A36R results in a direct interaction with the adaptor protein Nck and the recruitment of the Ena/VASP family member N-WASP to the site of actin assembly. We also show that Nck and N-WASP are essential for the actin-based motility of vaccinia virus. We suggest that vaccinia virus spreads by mimicking the signalling pathways that are normally involved in actin polymerization at the plasma membrane.     

Mox2 is a component of the genetic hierarchy controlling limb muscle development.

The skeletal muscles of the limbs develop from myogenic progenitors that originate in the paraxial mesoderm and migrate into the limb-bud mesenchyme. Among the genes known to be important for muscle development in mammalian embryos are those encoding the basic helix-loop-helix (bHLH) myogenic regulatory factors (MRFs; MyoD, Myf5, myogenin and MRF4) and Pax3, a paired-type homeobox gene that is critical for the development of limb musculature. Mox1 and Mox2 are closely related homeobox genes that are expressed in overlapping patterns in the paraxial mesoderm and its derivatives. Here we show that mice homozygous for a null mutation of Mox2 have a developmental defect of the limb musculature, characterized by an overall reduction in muscle mass and elimination of specific muscles. Mox2 is not needed for the migration of myogenic precursors into the limb bud, but it is essential for normal appendicular muscle formation and for the normal regulation of myogenic genes, as demonstrated by the downregulation of Pax3 and Myf5 but not MyoD in Mox2-deficient limb buds. Our findings show that the MOX2 homeoprotein is an important regulator of vertebrate limb myogenesis.     

The alcohol syndromes: the intrarecombigenic effect of acetaldehyde

Sister chromatid exchange was studied in lymphocyte and fibroblast cultures. Alcohol caused no disturbance under normal conditions but an acetaldehyde level above 40 muM inhibited cell multiplication and elevated SCE considerably. A high acetaldehyde level is thought to elicit the fetal alcohol syndrome, a view supported by clinical and experimental observations.     

氖和亚铜等离子蒸气系统中的负离子和电子能量分配函数

计算了激光产生铜等离子体蒸气中的物理和动力学参数，通过数值分析近似地求解玻尔兹曼动力学方程，发现存在一些具有各向同性和固定值物理量。在气体放电系统中观察了HBr混合物对其物理参数和电子能量分配函数的影响，利用交叉区电子碰撞激发过程计算了反应速度系数，表明具有HBr混合物的3d^94s^22D能级的共振激发更好。     

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy.

Malattia Leventinese (ML) and Doyne honeycomb retinal dystrophy (DHRD) refer to two autosomal dominant diseases characterized by yellow-white deposits known as drusen that accumulate beneath the retinal pigment epithelium (RPE). Both loci were mapped to chromosome 2p16-21 (refs 5,6) and this genetic interval has been subsequently narrowed. The importance of these diseases is due in large part to their close phenotypic similarity to age-related macular degeneration (AMD), a disorder with a strong genetic component that accounts for approximately 50% of registered blindness in the Western world. Just as in ML and DHRD, the early hallmark of AMD is the presence of drusen. Here we use a combination of positional and candidate gene methods to identify a single non-conservative mutation (Arg345Trp) in the gene EFEMP1 (for EGF-containing fibrillin-like extracellular matrix protein 1) in all families studied. This change was not present in 477 control individuals or in 494 patients with age-related macular degeneration. Identification of this mutation may aid in the development of an animal model for drusen, as well as in the identification of other genes involved in human macular degeneration.