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- W2100419893 abstract "Although indapamide has been used for many years as a first-line treatment of hypertension, it is only recently that some of its activities on the changes of the cardiovascular system, brought on by age and high blood pressure, have been studied. Indapamide appears to reduce blood pressure by a combined diuretic and direct vascular activity reducing vascular reactivity and total peripheral resistance. In addition, it has discrete effects on a number of interrelated systems that may protect the cardiovascular system. Indapamide reduces intracellular calcium levels, maintains magnesium ions, but reduces phosphate ions that may be involved in arterial rigidity. Circulating catecholamines remain unchanged but there is a reduction in normetanephrine, suggesting a reduction in sympathetic tone. It stimulates prostacyclin synthesis, increases levels of circulating prostacyclin, reduces platelet aggregation and stimulates the vasodilation elicited by endothelium-derived relaxing factor in the presence of bradykinin. In addition, it inhibits the formation of the vasoconstrictor prostanoid, thromboxane A2. The free radical scavenging activity of indapamide could also protect the vascular smooth muscle from the reperfusion injury of cerebral and myocardial ischemia. Indapamide induces a reduction in cerebral ischemia after carotid ligation. Unlike some other antihypertensives, it does not upset the high-density/low-density lipoprotein-cholesterol balance, reducing the possible risk of atherosclerosis. Moreover, the combination of binding to elastin and reduction in uptake of calcium and phosphate into the smooth muscle could be a mechanism for reducing arterial rigidity seen in the elderly and hypertensive patient. In hypertensive patients, these properties induce an improvement in arterial compliance, and in the long term a reduction in left ventricular hypertrophy. These pharmacologic and clinical results, together with a good antihypertensive efficacy and acceptability, suggest that indapamide may be a preferential agent in the long-term cardiovascular protection of the hypertensive patient." @default.
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- W2100419893 date "1990-05-01" @default.
- W2100419893 modified "2023-10-18" @default.
- W2100419893 title "Cardiovascular Protective Properties of Indapamide" @default.
- W2100419893 cites W1966034166 @default.
- W2100419893 cites W1968673882 @default.
- W2100419893 cites W1968898175 @default.
- W2100419893 cites W1971676288 @default.
- W2100419893 cites W1971681111 @default.
- W2100419893 cites W1972213372 @default.
- W2100419893 cites W1972851974 @default.
- W2100419893 cites W1973377271 @default.
- W2100419893 cites W1974372282 @default.
- W2100419893 cites W1978489723 @default.
- W2100419893 cites W1978883778 @default.
- W2100419893 cites W1980793899 @default.
- W2100419893 cites W1982230658 @default.
- W2100419893 cites W1987530942 @default.
- W2100419893 cites W1991370314 @default.
- W2100419893 cites W1993040817 @default.
- W2100419893 cites W1995324568 @default.
- W2100419893 cites W1999140943 @default.
- W2100419893 cites W1999413789 @default.
- W2100419893 cites W2007466575 @default.
- W2100419893 cites W2007737411 @default.
- W2100419893 cites W2008213689 @default.
- W2100419893 cites W2012249646 @default.
- W2100419893 cites W2013523129 @default.
- W2100419893 cites W2019609170 @default.
- W2100419893 cites W2025570799 @default.
- W2100419893 cites W2027764993 @default.
- W2100419893 cites W2027792004 @default.
- W2100419893 cites W2029904659 @default.
- W2100419893 cites W2030893656 @default.
- W2100419893 cites W2035171336 @default.
- W2100419893 cites W2038945674 @default.
- W2100419893 cites W2041353771 @default.
- W2100419893 cites W2041766687 @default.
- W2100419893 cites W2042353566 @default.
- W2100419893 cites W2042631424 @default.
- W2100419893 cites W2045073968 @default.
- W2100419893 cites W2046091450 @default.
- W2100419893 cites W2051281245 @default.
- W2100419893 cites W2052097767 @default.
- W2100419893 cites W2058298534 @default.
- W2100419893 cites W2063348355 @default.
- W2100419893 cites W2066266369 @default.
- W2100419893 cites W2070422165 @default.
- W2100419893 cites W2071166583 @default.
- W2100419893 cites W2071965463 @default.
- W2100419893 cites W2073550228 @default.
- W2100419893 cites W2073813597 @default.
- W2100419893 cites W2075507006 @default.
- W2100419893 cites W2078585951 @default.
- W2100419893 cites W2080600997 @default.
- W2100419893 cites W2083752249 @default.
- W2100419893 cites W2089002932 @default.
- W2100419893 cites W2089518282 @default.
- W2100419893 cites W2091474222 @default.
- W2100419893 cites W2091928279 @default.
- W2100419893 cites W2093518775 @default.
- W2100419893 cites W2104444078 @default.
- W2100419893 cites W2118090749 @default.
- W2100419893 cites W2119906106 @default.
- W2100419893 cites W2120426420 @default.
- W2100419893 cites W2123665694 @default.
- W2100419893 cites W2127992637 @default.
- W2100419893 cites W2129629768 @default.
- W2100419893 cites W2137771163 @default.
- W2100419893 cites W2141483250 @default.
- W2100419893 cites W2148343734 @default.
- W2100419893 cites W2153889942 @default.
- W2100419893 cites W2169182236 @default.
- W2100419893 cites W2170317646 @default.
- W2100419893 cites W2171687758 @default.
- W2100419893 cites W2335631045 @default.
- W2100419893 cites W2410636166 @default.
- W2100419893 cites W254792922 @default.
- W2100419893 cites W4236156127 @default.
- W2100419893 cites W4292764096 @default.
- W2100419893 cites W4300871367 @default.
- W2100419893 cites W54034763 @default.
- W2100419893 cites W69491808 @default.
- W2100419893 cites W76314274 @default.
- W2100419893 cites W1973472490 @default.
- W2100419893 doi "https://doi.org/10.1016/0002-9149(90)90337-z" @default.
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