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<title>General ionic magnesium dietary supplement research. nutrtional supplement 
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              <td valign="top" align="center" width="100%"><!-- #BeginLibraryItem "/Library/logo_general.lbi" --><p align="center"><img src="../../images/newlogo1.gif" alt="colloidal silver, ionic minerals, MSM, methylsufonylmethane, trace minerals, msm, colloidal silver generator, essential minerals, structured water, natural pet products, alternative health, arthritis pain relief, water filters, mineral supplements, glucosamine, chondroitin" border="0" align="center" width="455" height="60"></p>
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                <h3 class="fonts"><u>Research on the Mineral Magnesium</u></h3>
                <p align="left" class="mainfont">The following research abstracts 
                  are presented to reflect the findings of possible benefits from 
                  minerals as a dietary supplement and nutritional supplement. 
                  You will find more on the <a href="../../minerals/magnesium.html">ionic 
                  magnesium</a> page.</p>
                <h5 align="left" class="fonts">GENERAL MAGNESIUM RESEARCH</h5>
                <h5 align="left" class="fonts"><em> 
                  <!--++++++++ link1 ++++++++-->
                  <a name="general1">Magnesium sulfate therapy in certain emergency 
                  conditions</a></em></h5>
                <p align="left" class="mainfont">American Journal of Emergency 
                  Medicine (USA), 1997, 15/2 (182-187)</p>
                <p align="left" class="mainfont">Intravenous <font color="#0088AA">magnesium</font> 
                  has been suggested as a treatment for certain emergency conditions 
                  for more than 60 years. It is currently proposed to be beneficial 
                  in treating asthma, pre-eclampsia, eclampsia, myocardial infarction, 
                  and cardiac arrhythmias. The use and efficacy of the drug, however, 
                  are controversial. This article discusses the current state 
                  of <font color="#0088AA">magnesium</font> sulfate research and 
                  therapy.</p>
                <p align="center" class="mainc"><a href="./"><img src="../../images/back.gif" alt="back.gif" border="0" width="42" height="10"></a></p>
                <h5 align="left" class="fonts"><em> 
                  <!--++++++++ link2 ++++++++-->
                  <a name="general2">Magnesium metabolism in health and disease</a></em></h5>
                <p align="left" class="mainfont">DIS. MON. (USA), 1988, 34/4 (166-218)</p>
                <p align="left" class="mainfont">Magnesium is an important element 
                  for health and disease. Magnesium, the second most abundant 
                  intracellular cation, has been identified as a cofactor in over 
                  300 enzymatic reactions involving energy metabolism and protein 
                  and nucleic acid synthesis. Approximately half of the total 
                  <font color="#0088AA">magnesium</font> in the body is present 
                  in soft tissue, and the other half in bone. Less than 1% of 
                  the total body <font color="#0088AA">magnesium</font> is present 
                  in blood. Nonetheless, the majority of our experimental information 
                  comes from determination of <font color="#0088AA">magnesium</font> 
                  in serum and red blood cells. At present, we have little information 
                  about equilibrium among and state of <font color="#0088AA">magnesium</font> 
                  within body pools. Magnesium is absorbed uniformly from the 
                  small intestine and the serum concentration controlled by excretion 
                  from the kidney. The clinical laboratory evaluation of <font color="#0088AA">magnesium</font> 
                  status is primarily limited to the serum <font color="#0088AA">magnesium</font> 
                  concentration, 24-hour urinary excretion, and percent retention 
                  following parenteral <font color="#0088AA">magnesium</font>. 
                  However, results for these tests do not necessarily correlate 
                  with intracellular <font color="#0088AA">magnesium</font>. Thus, 
                  there is no readily available test to determine intracellular/total 
                  body <font color="#0088AA">magnesium</font> status. Magnesium 
                  deficiency may cause weakness, tremors, seizures, cardiac arrhythmias, 
                  hypokalemia, and hypocalcemia. The causes of hypomagnesemia 
                  are reduced intake (poor nutrition or IV fluids without <font color="#0088AA">magnesium</font>), 
                  reduced absorption (chronic diarrhea, malabsorption, or bypass/resection 
                  of bowel), redistribution (exchange transfusion or acute pancreatitis), 
                  and increased excretion (medication, alcoholism, diabetes mellitus, 
                  renal tubular disorders, hypercalcemia, hyperthyroidism, aldosteronism, 
                  stress, or excessive lactation). A large segment of the U.S. 
                  population may have an inadequate intake of <font color="#0088AA">magnesium</font> 
                  and may have a chronic latent <font color="#0088AA">magnesium</font> 
                  deficiency that has been linked to atherosclerosis, myocardial 
                  infarction, hypertension, cancer, kidney stones, premenstrual 
                  syndrome, and psychiatric disorders. Hypermagnesemia is primarily 
                  seen in acute and chronic renal failure, and is treated effectively 
                  by dialysis.</p>
                <p align="center" class="mainc"><a href="./"><img src="../../images/back.gif" alt="back.gif" border="0" width="42" height="10"></a></p>
                <h5 align="left" class="fonts"><em> 
                  <!--++++++++ link3 ++++++++-->
                  <a name="general3">Comparative findings on serum IMg<sup><small>2+</small></sup> 
                  of normal and diseased human subjects with the NOVA and KONE 
                  ISE's for Mg<sup><small>2+</small></sup></a></em></h5>
                <p align="left" class="mainfont">SCAND. J. CLIN. LAB. INVEST. 
                  SUPPL. (United Kingdom), 1994, 54/217</p>
                <p align="left" class="mainfont">It is clear now that although 
                  different ionophores for ionized Mg (IMg<sup><small>2+</small></sup>) 
                  have been designed by several groups, each of these has a distinctly 
                  different K(MgCa). In view of this, it is important to determine 
                  whether each of these ion selective electrodes (ISE's) yield 
                  identical results for IMg<sup><small>2+</small></sup> in sera 
                  from healthy and diseased humans. Using such an approach, we 
                  determined, in a blinded-and random manner, IMg<sup><small>2+</small></sup> 
                  with both the NOVA and KONE ISE's for IMg<sup><small>2+</small></sup> 
                  in two independent laboratories. No significant differences 
                  were found either for sera from healthy human volunteers or 
                  diseased patients. We did, however, note several interesting 
                  findings: 1. randomly, selected hospitalized patients exhibit 
                  a much higher incidence of abnormalities for IMg<sup><small>2+</small></sup> 
                  (57-71%) than that noted previously for total Mg (TMg) measurements; 
                  and 2. coronary heart disease, rectal cancer and multiple sclerosis 
                  patients exhibit extracellular deficits in ionized free Mg.</p>
                <p align="center" class="mainc"><a href="./"><img src="../../images/back.gif" alt="back.gif" border="0" width="42" height="10"></a></p>
                <h5 align="left" class="fonts"><em> 
                  <!--++++++++ link4 ++++++++-->
                  <a name="general4">Magnesium hormonal regulation and metabolic 
                  interrelations</a></em></h5>
                <p align="left" class="mainfont">PRESSE MED. (France), 1988, 17/12 
                  (584-587)</p>
                <p align="left" class="mainfont">Magnesium ion is of great importance 
                  in physiology by its intervention in 300 enzymatic systems, 
                  its role in membrane structure and its function in neuromuscular 
                  excitability. The skeleton is the first pool of <font color="#0088AA">magnesium</font> 
                  in the body. Intestinal absorption, renal metabolism, bone accretion 
                  and reabsorption of <font color="#0088AA">magnesium</font> are 
                  very similar to those of calcium. Magnesium metabolism is accurately 
                  controlled, in particular by parathyroid hormone, 25 - dihydroxy 
                  vitamin D3, calcitonin, catecholamine and estrogens. The main 
                  regulation mechanisms of <font color="#0088AA">magnesium</font> 
                  metabolism are located in the kidney which is the principal 
                  excretory organ.</p>
                <p align="center" class="mainc"><a href="./"><img src="../../images/back.gif" alt="back.gif" border="0" width="42" height="10"></a></p>
                <h5 align="left" class="fonts"><em> 
                  <!--++++++++ link5 ++++++++-->
                  <a name="general5">Thymic changes in the magnesium-depleted 
                  rat.</a></em></h5>
                <p align="left" class="mainfont">Alcock, N. W., Shils, M. E., 
                  Lieberman, P. H., &amp; Erlandson, R. A. <u>Cancer Research, 
                  33</u>, 2196-2204. (1973).</p>
                <p align="left" class="mainfont">The effects of a <font color="#0088AA">magnesium</font>-deficient 
                  diet fed to rats for approximately 65 days have been assessed 
                  with special reference to changes in the thymus. The thymus 
                  was enlarged in 18 to 52% of deficient animals surviving more 
                  than 6 to 7 weeks in various experiments. The remainder demonstrated 
                  glands that were smaller than controls. The enlarged thymuses 
                  showed marked cellular changes with the normal structure being 
                  replaced by cells that morphologically resembled transformed 
                  lymphocytes. Of the small glands, 19% had focal or lobular cellular 
                  changes similar to those seen in enlarged thymuses. No distant 
                  metastases were found and the changes have been interpreted 
                  as hyperplastic rather than neoplastic. Prolonged <font color="#0088AA">magnesium</font> 
                  depletion was accompanied by hypomagnesemia and hypercalcemia 
                  or normocalcemia. Marked leukocytosis was present during the 
                  early stages of the deficiency. Splenomegaly was consistently 
                  found in the <font color="#0088AA">magnesium</font>-depleted 
                  animals.<br>
                  Magnesium deficiency/ Rats/ Rodents/ Thymus</p>
                <p align="center"><a href="./"><img src="../../images/back.gif" alt="back.gif" border="0" width="42" height="10"></a></p>
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