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Lipids lowering

Ciprofibrate (48), a more potent lipid-lowering agent clofibrate, is prepared from Simmons-Smith product by Sandmeyer replacement of the amino group by a hydroxyl via the diazonium salt. Phenol undergoes the Reimer-Thiemann like process common to these agents upon alkaline treatment with acetone and chloroform to complete the synthesis of ci profib-rate (48). [Pg.44]

A lipid lowering agent of potential value in hypercholesterolemia is cetaben (31). It is synthesized facilely by monoalkylation of ethyl -aminobenzoate with hexadecyl bromide and then saponification. " ... [Pg.60]

HM74/-A Nicotinic acid Lipid lowering, anti-lipolytic... [Pg.181]

Lipid-lowering diugs are diugs that affect the lipoprotein metabolism and that used in therapy to lower plasma lipids (cholesterol, triglycerides). The main classes of... [Pg.690]

Although no drugs directly targeting the sterol transporters described above are available, the function of several lipid lowering diugs is associated with interaction with ABCA1. [Pg.1159]

In rodent stroke models, statin pretreatment has been shown to reduce infarct volumes and improve outcomes. Similarly, several clinical studies have shown that prior statin use reduced the severity of acute ischemic stroke and myocardial infarction. Recent studies indicate that beneftt can be achieved even when treatment is initiated after the onset of symptoms. In rodents, atorvastatin and simvastatin have been shown to reduce the growth of ischemic lesions, enhance functional outcome, and induce brain plasticity when administered after stroke onset. A retrospective analysis of the population-based Northern Manhattan Stroke Study (NOMASS) showed that patients using lipid-lowering agents at the time of ischemic stroke have a lower incidence of in-hospital stroke progression and reduced 90-day mortality rates. Retrospective analysis of data of the phase III citicoline trial showed... [Pg.101]

Elkind MS, Flint AC, Sciacca RR, Sacco RL. Lipid-lowering agent use at ischemic stroke onset is associated with decreased mortality. Neurology 2005 65 253-258. [Pg.116]

Corti R, Fayad ZA, Fuster V, Worthley SG, Helft G, Chesebro J, Mercuri M, Badimon JJ. Effects of lipid-lowering by simvastatin on human atherosclerotic lesions a longitudinal study by high-resolution, noninvasive magnetic resonance imaging. Circulation 2001 104(3) 249. [Pg.212]

Blood glucose and serum lipid lowering effects in humans with diabetes (McPeak et al., 2001 Rukmini et al., 2002 Qureshi et al., 2002). [Pg.355]

Other papers in the Symposium deal with the antioxidant and hypolipidemic effects of IP6, its chelating effects in heavy metal toxicity, inhibition of renal stones and other beneficial effects such as inhibition of platelet aggregation, inhibition of inflammatory responses (Shamsuddin, 1998). The lipid lowering effect and anti-neoplastic effect of 1P6 were extensively reviewed (Jariwalla, 1999). Hence, 1P6 is a valuable component of rice bran in preventing disease and maintaining health. 1P6 is present at 1.8-2% in rice bran. [Pg.361]

JARIWALLA R (1999) Inositol hexaphosphate (IP6) as an anti-neoplastic and lipid lowering agent. Anticancer Research, 19 3699-702. [Pg.372]

Lipid-lowering agents, 40 (2002) 1 5-Lipoxygenase inhibitors and their antiinflammatory activities, 29 (1992) 1 Literature of medicinal chemistry, 6 (1969) 266... [Pg.389]

Major outcomes in high-risk hypertensive patients randomized to angiotensin-converting enzyme inhibitor or calcium channel blocker vs. diuretic The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT). JAMA 2002 288(23) =2981-2997. [Pg.31]

The development of CHD is a lifelong process. Except in rare cases of severely elevated serum cholesterol levels, years of poor dietary habits, sedentary lifestyle, and life-habit risk factors (e.g., smoking and obesity) contribute to the development of atherosclerosis.3 Unfortunately, many individuals at risk for CHD do not receive lipid-lowering therapy or are not optimally treated. This chapter will help identify individuals at risk, assess treatment goals based on the level of CHD risk, and implement optimal treatment strategies and monitoring plans. [Pg.176]

TABLE 9-8. Effects of Lipid-Lowering Drugs on Serum Lipids at FDA-Approved Doses... [Pg.186]

Lipid-Lowering Drug LDL Cholesterol HDL Cholesterol Triglycerides Total Cholesterol... [Pg.186]

TABLE 9-9. Formulation, Dosing, and Common Adverse Effects of Lipid-Lowering Drugs... [Pg.187]

Lipid-Lowering Drug Dosage Forms Usual Adult Maintenance Dose Range Adverse Effects... [Pg.187]

Bea F, Blessing E, Shelley MI, Shultz JM, Rosenfeld ME. Simvastatin inhibits expression of tissue factor in advanced atherosclerotic lesions of apolipoprotein E deficient mice independently of lipid lowering potential role of simvastatin-mediated inhibition of Egr-1 expression and activation. Atherosclerosis 2003 167(2) 187-194. [Pg.223]


See other pages where Lipids lowering is mentioned: [Pg.44]    [Pg.186]    [Pg.228]    [Pg.598]    [Pg.598]    [Pg.690]    [Pg.1495]    [Pg.203]    [Pg.17]    [Pg.20]    [Pg.30]    [Pg.43]    [Pg.72]    [Pg.74]    [Pg.102]    [Pg.104]    [Pg.179]    [Pg.181]    [Pg.188]    [Pg.662]    [Pg.848]    [Pg.848]    [Pg.220]    [Pg.432]    [Pg.176]    [Pg.163]    [Pg.267]    [Pg.267]    [Pg.268]    [Pg.268]    [Pg.269]   
See also in sourсe #XX -- [ Pg.437 ]




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