Ionic Basis of Hypertension in Diabetes Mellitus

Abstract
Alterations of cell ion content have been reported acutely after oral glucose ingestion, and chronically in subjects with hypertension and noninsulin dependent diabetes mellitus (NIDDM). We have hypothesized that these ionic abnormalities, elevated cytosolic free calcium (Cai), and suppressed intracellular pH (pHi) and free magnesium (Mgi), common to both of these syndromes, may explain their frequent clinical coincidence. To investigate the potential role of glucose in this process, we utilized 19F- and 31P-NMR spectroscopy to measure Cai Mgi, and pHi in normal human red blood cells before and 60, 120, and 180 min after in vitro incubation with glucose (15 mmol/L) and equimolar concentrations of the glucose analogs, L-glucose, 2-deoxyglucose, and 3-O-methylglucose. At each point in time (from t = 0 to t = 60, 120, 180 min), glucose induced significant (P < .05) elevations in Cai (27.2 ± 2.2 to 68.3 ± 7.2, 70.7 ± 10.5, 59.8 ± 10.1nmol/L), while suppressing pHi (7.28 ± 0.02 to 7.22 ± 0.03, 7.23 ± 0.03, 7.22 ± 0.03), and Mgi (206 ± 10 to 151 ± 7,131 ± 7 , 143 ± 5 μmol/L ). This glucose induced ionic effect was dose dependent, significant elevations in Cai being observed at 10 and 15 mmol/L, but not at the other concentrations tested. It was also specific, no changes in Cai being observed with any of the glucose analogs tested. Thus, hyperglycemia per se elevates Cai and suppresses Mgi and pHi in normal human red cells. Since these abnormalities are exactly those observed in essential as well as diabetic hypertension, our results suggest that glucose levels, independent of insulin, may contribute to cellular ion homeostasis, and thus risk hypertension and vascular disease in people with diabetes. Am J Hypertens 1993;6:413–417