2009
DOI: 10.1016/j.metabol.2009.01.013
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Circulating angiotensin II is associated with body fat accumulation and insulin resistance in obese subjects with type 2 diabetes mellitus

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Cited by 67 publications
(62 citation statements)
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References 41 publications
(59 reference statements)
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“…Angiotensin II was also considered an important mechanism in ORG, similar to TNF-α and MCP-1 [26, 27]. Plasma angiotensin II was associated with BW and visceral fat area and decreased during weight reduction in obese subjects with type 2 diabetes [39]. Angiotensin II suppressed LPL production in 3T3-L1 cells, and valsartan, an angiotensin II receptor antagonist, increased preheparin LPL level in type 2 diabetes with hypertension [17, 40].…”
Section: Discussionmentioning
confidence: 99%
“…Angiotensin II was also considered an important mechanism in ORG, similar to TNF-α and MCP-1 [26, 27]. Plasma angiotensin II was associated with BW and visceral fat area and decreased during weight reduction in obese subjects with type 2 diabetes [39]. Angiotensin II suppressed LPL production in 3T3-L1 cells, and valsartan, an angiotensin II receptor antagonist, increased preheparin LPL level in type 2 diabetes with hypertension [17, 40].…”
Section: Discussionmentioning
confidence: 99%
“…It has been documented that the RAS is linked to obesity and its activity is reduced in association with WL. 46,47 Such reduction in RAS is important for renal protection. 48,49 A recent study by our group in Caucasian subjects demonstrated that exercise, but not calorie restriction, contributed more to improvements in renal function and suppression of plasma renin activity.…”
Section: Discussionmentioning
confidence: 99%
“…Ang II would then bind to the Ang II type 1 receptor (AT1R) and induce signaling pathways that promote muscle constriction, salt and water retention, fibrosis, hypertrophy, and hyperplasia that underlie many metabolic diseases and poor cardiovascular and renal prognosis. Blockade of RAS can be exerted at multiple levels, via inhibition of renin, ACE, or AT1R signaling [6,7,8,9,10,11,12]. Efficient RAS blockers at all these levels have been developed and are currently in use to block overactivation of RAS and to offer protection from RAS-related metabolic diseases including diabetes [8,9,10,11,12,13].…”
Section: Introductionmentioning
confidence: 99%