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131.
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This study examines the incorporation of highly unsaturated n−3 fatty acids (HUFA) into triacylglycerols (TAG) of brown adipose
tissue (BAT), and their effect on the positional distribution of saturated (SFA) and of unsaturated (UFA) 16- or 18-carbon
fatty acids. To this end, rats were fed a fish oil diet for up to four weeks. The stereospecific analysis of TAG was based
on generation ofsn-1,2- andsn-2,3-acylglycerols by Grignard degradation, followed by synthesis of phosphatidic acid and specific hydrolysis with phospholipase
A2. From the end of the first week of fish oil feeding, a steady-state in the fatty acid composition of TAG in BAT was reached.
HUFA concentration increased 30-fold, mainly at the expense of n−9 UFA and of SFA. The amount of SFA decreased selectively
at position 3, where these fatty acids were progressively replaced by n−3 HUFA. By contrast, the amount of UFA decreased at
all positions, and their positional distribution was not affected. About 60% of HUFA was incorporated at position 3. Nearly
twice as much 22∶6n−3 was incorporated into TAG than had been previously observed in white adipose tissue (WAT) [Leray, C.,
Raclot, T., and Groscolas, R. (1993)Lipids 28, 279–284]. At the steady-state, the distribution of HUFA was characterized by high proportions of 22∶6n−3 and 20∶5n−3 in
position 3. Moreover, in each position of TAG, a steady level was reached rapidly (within 1 wk). It is concluded that, during
fish-oil feeding, fatty acids in TAG of BAT show characteristic time-course changes that lead to a characteristic composition
and a tissue-specific positional distribution. This suggests that adipose tissue has its own specificity in controlling the
build-up of TAG stores, which is likely to be regulated by the specificity of acylating enzymes as well as molecular rearrangements. 相似文献
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136.
The modification of the mechanical properties of polypyrrole (PPY) by electrochemical preparation of conductive composite film from pyrrole (PY) and three kinds of liquid crystalline copoly(ester-amide)—PEA(H), PEA(C), PEA(O)—are presented. The electrical conductivity of the PEA(H)/PPY, PEA(C)/PPY, and PEA(O)/PPY composites are the same order of magnitude as PPY. The mechanical properties of the composite films are much better than that of pure PPY, and the composite films have good conductivity and thermostability. © 1994 John Wiley & Sons, Inc. 相似文献
137.
138.
Ana Paula Vieira Soares Manuel Farinha Portela Alain Kiennemann 《Catalysis Reviews》2005,47(1):125-174
This review deals with the important industrial reaction of formaldehyde manufacture by methanol oxidation over iron molybdate catalysts. Detailed reference is made to the used catalyst, preparation techniques (coprecipitation, sol-gel like, mechanical mixing, etc.) including unsupported and supported catalysts, promoters and characterization methods. The controversial active phase assignment (stoichiometric versus Mo rich iron molybdate) is discussed. The proposed reaction mechanisms and kinetic laws for the main and side reactions are examined. The catalyst deactivation processes are reviewed and the role of Mo excess on these processes is underlined. Finally conclusions and perspectives are presented. 相似文献
139.
以1-丁烯(B t)为原料,负载钛(简称Ti)-三异丁基铝(简称Al)为催化体系,用本体聚合法合成了聚1-丁烯(PBt)热塑性弹性体(TPE)。考察了聚合条件对PBt TPE的影响,并用差示扫描量热法对聚合物进行了分析。结果表明,随着氢气压力的升高,单体转化率、催化效率呈下降趋势;随着Al/Ti(摩尔比)的增加,转化率和催化效率先升高后降低;随着Ti/Bt(摩尔比)的增加,转化率和催化效率逐渐升高;随着聚合温度的升高,转化率和催化效率先升高后降低;在氢气压力为0.2 MPa、Al/Ti为300、Ti/Bt为2×10-5、反应温度为30℃的聚合条件下,合成出转化率为80.0%的PBt TPE。随着氢气压力的升高,聚合物的特性黏数([η])和全同立构质量分数都呈下降趋势,氢气压力能较好地调节聚合物的相对分子质量;随着Al/Ti的增加,[η]逐渐下降,全同立构质量分数变化不明显;随着Ti/Bt的增加,[η]先升高后降低,最后趋于平稳,而全同立构质量分数略有降低后趋于平稳;随着聚合温度的升高,[η]和全同立构质量分数都呈下降趋势。反应温度为40℃时,PBt TPE的结晶度最高,为20.3%。 相似文献
140.
A kinetic study of the anionic polymerization of ethylene oxide has been made in tetrahydrofuran at 20°C, with the cryptate Cs+ + [TC] as counterion, [TC] being a spheroidal macrotricyclic ligand. Conductance measurements have been made on THF solutions of ?4BCs + [TC]. Ionic associations higher than cryptated ion pairs are negligible for living end concentrations lower than 3 × 10?4 moll?1. k± and the alkoxide ion pair dissociation constant KD were determined from both sets of kinetic data obtained with and without added salt knowing the value of k? from kinetic data performed with K+ + [222] as counterion. Free alkoxide ions are about twenty times more reactive than cryptated caesium ion pairs. 相似文献