आईएसएसएन: 2165-7904

मोटापा और वजन घटाने की थेरेपी जर्नल

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

में अनुक्रमित
  • सूचकांक कॉपरनिकस
  • गूगल ज्ञानी
  • जे गेट खोलो
  • जेनेमिक्स जर्नलसीक
  • सेंटर फॉर एग्रीकल्चर एंड बायोसाइंसेज इंटरनेशनल (CABI)
  • RefSeek
  • हमदर्द विश्वविद्यालय
  • ईबीएससीओ एज़
  • ओसीएलसी- वर्ल्डकैट
  • एसडब्ल्यूबी ऑनलाइन कैटलॉग
  • CABI पूरा पाठ
  • कैब डायरेक्ट
  • पबलोन्स
  • चिकित्सा शिक्षा और अनुसंधान के लिए जिनेवा फाउंडेशन
  • यूरो पब
  • ब्रिस्टल विश्वविद्यालय
  • PubMed
  • आईसीएमजेई
इस पृष्ठ को साझा करें

अमूर्त

The Role of Triacylglycerol in the Oxidizability of Low Density Lipoproteins and High Density Lipoproteins: Possible Contributions to Atherosclerosis in Metabolic Syndrome

Roberta Cazzola, Gabriele Piuri, Micaela Garziano, Erica Cassani, Anna Boggio, Michela Barichella, Fulvio Muzio and Benvenuto Cestaro

Objective: Metabolic Syndrome (MetS) is a cluster of Cardio-Vascular Disease (CDV) risk factors including visceral obesity, hyperglycemia, hypertension, low HDL cholesterol, hypertriglyceridemia and increased oxidative stress. Pyrene-lipid derivatives selectively incorporated into the hydrophobic core and surrounding amphipathic envelope of LDLs and HDLs are useful markers of the oxidizability of these lipoprotein regions. We performed an observational study aimed at investigating the effect of lipid composition, in particular triacylglycerol (TAG) levels, on the oxidizability of the core and the envelope of LDLs and HDLs in MetS.
Methods: We induced changes in the chemical composition of lipoprotein in vivo by placing on a hypocaloric balanced diet fifteen overweight and moderately obese men (BMI: 25-35 kg/mq) with MetS until they lost at least 5% of their initial weight. The core and the surface of LDLs and HDLs were labeled with selective pyrenic probes. Susceptibility to 2,2'-azobis-2-methyl-propanimidamide-dihydrochloride-induced peroxidation was measured following kinetically the decrease of fluorescence of these probes. The length of the lag phase (lag-time) of peroxidation kinetic were calculated and used as indices of lipoprotein oxidizability. In addition, we measured paraoxonase activity and plasma oxidative status.
Results: After weight loss, together with a reduction of triglyceridemia and the improvement of the other CDV risk factors associated with MetS, we observed a massive transfer of TAG from HDLs toward LDLs. In the LDLs core, the increased TAG concentration halved the resistance to peroxidation, while in the HDLs core the reduction of this parameter doubled the value of lag-time. In the lipoprotein hydrophobic cores, the duration of lag-time correlated directly with ratio between cholesteryl esters and TAG. No significant changes were found in paraoxonase activity and plasma oxidative status.
Conclusions: Less oxidizable HDLs, but also more oxidizable LDLs seem to accompany the improvement of different metabolic factors induced by weight loss in obese men with MetS.