The primary goal of this research continues to be elucidation of intracellular metal ion (Na+, K+, free Mg2+ & free Ca2+) metabolism in normal and pathological states. We seek to understand how the regulation of intracellular concentrations of essential metal ions goes astray in health disorders, especially hypertension diabetes. Our main research tool is NMR spectroscopy. Our laboratory played a key role in the development of NMR methods for measuring intracellular Na+ (using a membrane-impairment extracellular shift reagent to differentiate between intra- and extracellular ions) and free Mg2+ (by analyzing 31P NMR chemical shifts of intracellular ATP), and for simultaneous measurement of heavy metals and intracellular free Ca2+ (by 19F NMR of fluorinated probe molecules introduced into the cell). The choice of cells and issues for our research is based on the criteria of availability and physiological significance. It includes human peripheral blood cells (erythrocytes and platelets), intact rat kidney and heart in-vivo or perfused in vitro, and perfused rat aorta which is a readily accessible model for vascular smooth muscle cells. The following specific aims will be pursued: (l) To test the hypothesis that intracellular potassium deficit is relevant in hypertension, and arises due to increased K+ efflux via calcium-activated potassium channels; 2) To test the hypothesis that an abnormality in renal sodium transport due to hyperactivity of renal Na+:H+ transport accompanies vascular ionic changes in salt-sensitive, but not in salt-resistant, essential hypertension: 3) To investigate the effects of diabetes on intracellular [Na+], [K+], free [Ca2+], free [Mg2+] and pH in elected target tissues (kidney, heart and vasculature) in diabetic rat models;(4) To investigate the potential ole of hyperglycemia in causing diabetes associated intracellular ionic abnormalities, especially in the vascular tissue; and (5) To investigate increased vulnerability of diabetic and hypertensive kidney and myocardium to ischemic damage, and the protective effect of magnesium ions. It is hoped that the proposed investigations of intracellular ions in hypertension and diabetes will eventually lead to better strategies for he management of these health disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK032030-15
Application #
2518260
Study Section
Metallobiochemistry Study Section (BMT)
Program Officer
Linder, Barbara
Project Start
1982-05-01
Project End
1999-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
15
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Physiology
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Altura, Burton M; Kostellow, Adele B; Zhang, Aimin et al. (2003) Expression of the nuclear factor-kappaB and proto-oncogenes c-fos and c-jun are induced by low extracellular Mg2+ in aortic and cerebral vascular smooth muscle cells: possible links to hypertension, atherogenesis, and stroke. Am J Hypertens 16:701-7
Li, W; Zheng, T; Babu, A N et al. (2001) Importance of magnesium ions in development of tolerance to ethanol: studies on cultured cerebral vascular smooth muscle cells, type-2 astrocytes and intact rat brain. Brain Res Bull 56:153-8
Resnick, L M; Barbagallo, M; Dominguez, L J et al. (2001) Relation of cellular potassium to other mineral ions in hypertension and diabetes. Hypertension 38:709-12
Barbagallo, M; Gupta, R K; Dominguez, L J et al. (2000) Cellular ionic alterations with age: relation to hypertension and diabetes. J Am Geriatr Soc 48:1111-6
Chi, Y; Gupta, R K (1998) Alterations in heart and kidney membrane phospholipids in hypertension as observed by 31P nuclear magnetic resonance. Lipids 33:1023-30
Altura, B M; Gebrewold, A; Zhang, A et al. (1998) Magnesium deficiency exacerbates brain injury and stroke mortality induced by alcohol: a 31P-NMR in vivo study. Alcohol 15:181-3
Chi, Y; Gupta, R K (1998) Alterations in membrane fatty acid unsaturation and chain length in hypertension as observed by 1H NMR spectroscopy. Am J Hypertens 11:340-8
Morrill, G A; Gupta, R K; Kostellow, A B et al. (1998) Mg2+ modulates membrane sphingolipid and lipid second messenger levels in vascular smooth muscle cells. FEBS Lett 440:167-71
Altura, B M; Gebrewold, A; Zhang, A et al. (1997) Short-term reduction in dietary intake of magnesium causes deficits in brain intracellular free Mg2+ and [H+]i but not high-energy phosphates as observed by in vivo 31P-NMR. Biochim Biophys Acta 1358:1-5
Barac-Nieto, M; Gupta, R K (1996) Use of proton MR spectroscopy and MR imaging to assess obesity. J Magn Reson Imaging 6:235-8

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