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Calcium, hypertension

Calcium Hypertension, pregnancy-induced hypertension, and preeclampsia... [Pg.2506]

Calcium channel blockers reduce arterial blood pressure by decreasing calcium influx, resulting in a decrease in intracellular calcium (236,237). The arterial smooth muscle tone decreases, thereby decreasing total peripheral resistance. The increase in vascular resistance in hypertension is found to depend much on calcium influx. Calcium channel blockers reduce blood pressure at rest and during exercise. They decrease the transmembranous calcium influx or entry that lead to a net decrease of intracellular calcium and therefore the vascular tone falls, as does blood pressure. [Pg.141]

Calcium channel blockers normalize the blood pressure in about 80% of hypertensive patients older than 60 years of age, 50% of those between 40 and 60 years of age, and only 20% of patients under 40 years of age. Thus calcium channel blockers are best for patients who are elderly and have low PRA and mosdy ineffective in patients who have high PRA. This responsiveness profile is very similar to that of the diuretics. [Pg.142]

Calcium channel blockers cause more pronounced lowering of blood pressure in hypertensive patients than in normotensive individuals. Generally, all calcium channel blockers cause an immediate increase in PRA during acute treatment in patients having hypertension but PRA is normalized during chronic treatment despite the sustained decrease in blood pressure. These agents also do not generally produce sodium and water retention, unlike the conventional vasodilators. This is because they produce diuretic effects by direct actions on the kidney. [Pg.142]

Verapamil (Table 1), the first slow channel calcium blocker synthesized to selectively inhibit the transmembrane influx of calcium ions into cells, lowers blood pressure in hypertensive patients having good organ perfusion particularly with increased renal blood flow. Sustained-release verapamil for once a day dosing is available for the treatment of hypertension. Constipation is a prominent side effect. Headache, dizziness, and edema are frequent and verapamil can sometimes cause AV conduction disturbances and AV block. Verapamil should not be used in combination with -adrenoceptor blockers because of the synergistic negative effects on heart rate and contractile force. [Pg.142]

Industrial uses make up most of the market for cyanamide. Calcium cyanamide is used directly for steel nitridation (34) and to some extent for desulfurization (36) (see Steel). Cyanamide is used to produce cationic starch (36) and calcium cyanide. Cyanamide is, of course, the raw material for dicyandiamide and melamine. New uses include intermediates for pesticides, detergents (37), medicines such as antihistamines, hypertension, sedatives, contraceptives, etc (38), the photography industry (39), as an additive for fuels and lubricants, as a paper preservative, and as a cement additive. [Pg.370]

The sales of oral diuretics are declining, and are forecast to continue their decline in constant dollars during the 1990s (119,120). Several possible explanations can be offered for these trends. The patents of market leaders are expiring, lea ding to the introduction of generic brands at ca 40% below the cost of the branded market leaders physicians are switching to newer treatments for hypertension, eg, calcium channel blockers and... [Pg.213]

Procardia XL. Procardia XL extended-release capsules, marketed by Pfizer Labs Division of Pfizer, Inc., contain nifedipine [21829-25-4] a calcium channel blocker of mol wt 346.3. The extended release tablet is formulated as a once-a-day controlled release capsule for oral adrninistration dehvering either 30, 60, or 90 mg nifedipine. Procardia XL is indicated for use in the management of vasospastic angina, chronic stable angina, and hypertension (see Cardiovascularagents). [Pg.232]

ATPase inhibitor. In such patients, inhibition of the sodium pump in the cells lining the blood vessel wall results in accumulation of sodium and calcium in these cells and the narrowing of the vessels to create hypertension. An 8-year study aimed at the isolation and identification of the agent responsible for these effects by researchers at the University of Maryland Medical School and the Upjohn Laboratories in Michigan recently yielded a surprising result. Mass spectrometric analysis of compounds isolated from many hundreds of gallons of blood plasma has revealed that the hypertensive agent is ouabain itself or a closely related molecule ... [Pg.304]

The so-called calcium channel blockers constitute a class of cardiovascular agents that have gained prominence in the past few years. These drugs, which obtund contraction of arterial vessels by preventing the movement of calcium ions needed for those contractions, have proved especially useful in the treatment of angina and hypertension. Dihydropyridines such as nifedipine (30) are par-... [Pg.149]

In the treatment of hypertension, ACE inhibitors are as effective as diuretics, (3-adrenoceptor antagonists, or calcium channel blockers in lowering blood pressure. However, increased survival rates have only been demonstrated for diuretics and (3-adrenoceptor antagonists. ACE inhibitors are approved for monotherapy as well as for combinational regimes. ACE inhibitors are the dtugs of choice for the treatment of hypertension with renal diseases, particularly diabetic nephropathy, because they prevent the progression of renal failure and improve proteinuria more efficiently than the other diugs. [Pg.10]

ACE inhibitors - AT antagonists - Alpha blockers - Beta blockers Isolated syslolic hypertension (older patienls) - Diuretics preferred (generally Thiazides) - Long-acting dihydropyridine calcium channel blocker... [Pg.143]

Uehata M, Ishizaki T, Satoh H et al (1997) Calcium sensitization of smooth muscle mediated by a Rho-associated protein kinase in hypertension. Nature 389 990-994... [Pg.1145]

Benzothiazepines belong to the three classes of calcium channel blockers which are important cardiovascular drugs in the management of angina pectoris and hypertension. A diastereoselective one-pot synthesis of the trans-and ds-3-hydroxy-2-(4-methoxyphenyl)-2,3-dihydro-l,5-benzothiazepin-4-one nucleus, a key intermediate in the preparation of the calcium channel blocker Diltiazem, was carried out under microwave irradiation in an open vessel (Scheme 25). Control of the diastereoselectivity was achieved by vary-... [Pg.74]

BP, blood pressure CCB, calcium channel blocker agent DBP, diastolic blood pressure SBP, systolic blood pressure. (Adapted from JNC 7 Modified from Saseen JJ, Carter BL. Hypertension. In DiPiro JT, Talbert RL, Yee GC, et al, (eds.) Pharmacotherapy A Pathophysiologic Approach. 6th ed. New York McGraw-Hill 2005 194, with permission.)... [Pg.11]


See other pages where Calcium, hypertension is mentioned: [Pg.377]    [Pg.377]    [Pg.250]    [Pg.445]    [Pg.23]    [Pg.125]    [Pg.126]    [Pg.132]    [Pg.140]    [Pg.142]    [Pg.212]    [Pg.526]    [Pg.305]    [Pg.106]    [Pg.7]    [Pg.140]    [Pg.142]    [Pg.144]    [Pg.321]    [Pg.431]    [Pg.1304]    [Pg.1304]    [Pg.381]    [Pg.394]    [Pg.402]    [Pg.471]    [Pg.37]    [Pg.257]    [Pg.497]    [Pg.169]    [Pg.292]    [Pg.77]    [Pg.194]    [Pg.13]    [Pg.21]    [Pg.24]   
See also in sourсe #XX -- [ Pg.329 ]




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