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生物体内甜菜碱脂的研究进展 被引量:2
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作者 翁倩 徐继林 +1 位作者 周成旭 严小军 《生物学杂志》 CAS CSCD 2015年第2期87-91,109,共6页
甜菜碱脂是一类极性膜脂,自然界中发现的有3类,分布于不同类别的生物中,其中最广泛分布于藻类以及部分低等植物中,有着多种功能,最主要的作用是作为膜脂参与生物的生命活动,对光合作用、植物抗逆以及藻类生物燃料的开发具有重要意义。... 甜菜碱脂是一类极性膜脂,自然界中发现的有3类,分布于不同类别的生物中,其中最广泛分布于藻类以及部分低等植物中,有着多种功能,最主要的作用是作为膜脂参与生物的生命活动,对光合作用、植物抗逆以及藻类生物燃料的开发具有重要意义。不同生物体中的甜菜碱脂类别、含量以及分布均有差异,对甜菜碱脂的结构、化学鉴定、细胞内定位、理化性质、生物合成及其分子生物学机理等多方面进行综述,并指出目前研究中仍需解决的问题、可以拓展的方向,以便于对甜菜碱脂进行更为深入地研究。 展开更多
关键词 甜菜碱脂 DGTS DGTA DGCC
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甜菜碱脂在14种海洋微藻中的分布研究 被引量:1
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作者 李艳荣 牟桐 +3 位作者 黄莉莉 徐继林 周成旭 严小军 《海洋学报》 CAS CSCD 北大核心 2020年第12期72-81,共10页
采用超高效液相色谱−四极杆−飞行时间质谱联用分析系统(UPLC-Q-TOF MS),对4个微藻门中的14种微藻的甜菜碱脂的分子组成及其相应脂肪酸的组成及分布进行分析。结果表明:在14种微藻中共鉴定出133种甜菜碱脂,包括53种DGCC、41种DGTS和39种D... 采用超高效液相色谱−四极杆−飞行时间质谱联用分析系统(UPLC-Q-TOF MS),对4个微藻门中的14种微藻的甜菜碱脂的分子组成及其相应脂肪酸的组成及分布进行分析。结果表明:在14种微藻中共鉴定出133种甜菜碱脂,包括53种DGCC、41种DGTS和39种DGTA。其中甲藻和定鞭藻中主要的甜菜碱脂种类为DGCC,绿藻中主要的甜菜碱脂种类为DGTS;而在硅藻中的甜菜碱脂主要包括两种:中心硅藻纲中为DGCC,羽纹硅藻纲中为DGTA。此外,不同微藻中甜菜碱脂脂肪酸组成差异仅限制在门或纲的水平上,在较低的分类水平上差异不明显。硅藻门、甲藻门和定鞭藻门中均含有DGCC,其脂肪酸链的组成均含有C14−C18的脂肪酸以及C20和C22的多不饱和脂肪酸,但是甲藻的C14−C18脂肪酸链为饱和的,而C19奇数碳原子的脂肪酸链仅在硅藻中发现。认为海洋微藻甜菜碱脂的研究可以为海洋微藻化学分类学以及缺磷极性脂类的生理、生态作用和功能特性研究提供重要参考依据。 展开更多
关键词 海洋微藻 甜菜碱脂 超高效液相色谱−四极杆−飞行时间质谱
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Betaine and nonalcoholic steatohepatitis: Back to the future? 被引量:7
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作者 Sandeep Mukherjee 《World Journal of Gastroenterology》 SCIE CAS CSCD 2011年第32期3663-3664,共2页
Nonalcoholic steatohepatitis (NASH) is an important indication for liver transplantation in many Western countries. Obesity and insulin resistance are the two most common risk factors for NASH, which can lead to recur... Nonalcoholic steatohepatitis (NASH) is an important indication for liver transplantation in many Western countries. Obesity and insulin resistance are the two most common risk factors for NASH, which can lead to recurrent NASH after liver transplantation. There is currently no approved therapy for NASH, and treatment is directed at risk factor modification and lifestyle changes. Betaine has been used for NASH, with mixed results, and may show promise in conjunction with other agents in clinical trials. 展开更多
关键词 BETAINE Nonalcoholic steatohepatitis CIRRHOSIS OBESITY Insulin resistance
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Role of transmethylation reactions in alcoholic liver disease 被引量:3
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作者 Kusum K Kharbanda 《World Journal of Gastroenterology》 SCIE CAS CSCD 2007年第37期4947-4954,共8页
Alcoholic liver disease is a major health care problem worldwide. Findings from many laboratories, including ours, have demonstrated that ethanol feeding impairs several of the many steps involved in methionine metabo... Alcoholic liver disease is a major health care problem worldwide. Findings from many laboratories, including ours, have demonstrated that ethanol feeding impairs several of the many steps involved in methionine metabolism. Ethanol consumption predominantly results in a decrease in the hepatocyte level of S-adenosylmethionine and the increases in two toxic metabolites, homocysteine and S-adenosylhomocysteine. These changes, in turn, result in serious functional consequences which include decreases in essential methylation reactions v/a inhibition of various methyltransferases. Of particular interest to our laboratory is the inhibition of three important enzymes, phosphatidylethanolamine methyltransferase, isoprenylcysteine carboxyl methyltransferase and protein L-isoaspartate methyltransferase. Decreased activity of these enzymes results in increased fat deposition, increased apoptosis and increased accumulation of damaged proteins- all of which are hallmark features of alcoholic liver injury. Of all the therapeutic modalities available, betaine has been shown to be the safest, least expensive and most effective in attenuating ethanol-induced liver injury. Betaine, by virtue of aiding in the remethylation of homocysteine, removes both toxic metabolites (homocysteine and S-adenosylhomocysteine), restores S-adenosylmethionine level, and reverses steatosis, apoptosis and damaged proteins accumulation. In conclusion, betaine appears to be a promising therapeutic agent in relieving the methylation and other defects associated with alcoholic abuse. 展开更多
关键词 TRANSMETHYLATION S-ADENOSYLHOMOCYSTEINE ALCOHOL BETAINE Liver STEATOSIS Apoptosis METHYLTRANSFERASES
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