Cellular ionic alterations with age: Relation to hypertension and diabetes

被引:60
作者
Barbagallo, M
Gupta, RK
Dominguez, LJ
Resnick, LM
机构
[1] Cornell Univ, Med Ctr, New York Presbyterian Hosp, Hypertens Ctr, New York, NY 10021 USA
[2] Univ Palermo, Inst Internal Med & Geriatr, Palermo, Italy
[3] Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10467 USA
[4] Wayne State Univ, Med Ctr, Div Endocrine Hypertens, Detroit, MI 48202 USA
关键词
calcium; magnesium; aging; hypertension; diabetes;
D O I
10.1111/j.1532-5415.2000.tb04788.x
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
BACKGROUND: Cytosolic free calcium (Cai) and magnesium (Mgi) are vital to cellular homeostasis and function. OBJECTIVE: To evaluate cellular divalent cations in normal subjects at different ages and their relationship to ion levels in essential, hypertension and diabetes. DESIGN: A cross-sectional study. SETTING: A university hospital in New York. PARTICIPANTS: A total of 103 subjects (32 older, 71.1 +/- 1.2 y/o, and 71 young/middle aged subjects, 51.1 +/- 2.3 y/o). INTERVENTION: Oral glucose tolerance test. MEASUREMENTS: F-19 and P-31 NMR spectroscopy were used to measure Cai and Mgi levels in erythrocytes from normal (>65 y/o, n = 11; <65 y/o, n = 26), hypertensive (EH) (>65 y/o, n = 9; <65 y/o, n = 30), and type 2 diabetic (DM) (>65 y/o, n = 12; <65 y/o, n = 15) subjects; these levels were also compared with glucose and insulin levels before and after oral glucose loading. RESULTS: Fasting Mgi levels were lower (207 +/- 7.8 vs 236 +/- 7.5 mu M; P < .05) and Cai higher (32.2 +/- 3.0 vs 20.3 +/- 1.8 nM; P < .05) in older than in younger normal subjects. For all normal subjects, the greater the age, the higher the Cai (r = 0.622, P = .004) and the lower the Mgi (r = -0.423; P = .011). However, no significant (P = NS) differences in Mgi or Cai levels were observed between older normal and young/middle-aged subjects with EH (Mgi = 189.7 +/- 5.9 vs 182.6 +/- 9.8 mu M; Cai = 33.8 +/- 4.9 vs 35.6 +/- 4.0 nM) or DM (Mgi = 182.8 +/- 10.9 vs 180.8 +/- 8.1 mu M; Cai = 33.6 +/- 4.3 vs 39.7 +/- 5.9 nM). Significant relationships were also found between cellular ion content, blood pressure, and glycemic indices. CONCLUSIONS: Aging is associated with the onset of altered Cai and Mgi levels, indistinguishable from those observed in hypertension and diabetes, independent of age. We suggest that these ionic changes may be clinically significant, underlying the predisposition of older subjects to cardiovascular and metabolic diseases.
引用
收藏
页码:1111 / 1116
页数:6
相关论文
共 57 条
  • [1] STUDY OF ANTIOXIDANT PROPERTIES OF METAL ASPARTATES
    AFANASEV, IB
    SUSLOVA, TB
    CHEREMISINA, ZP
    ABRAMOVA, NE
    KORKINA, LG
    [J]. ANALYST, 1995, 120 (03) : 859 - 862
  • [2] ALTURA BM, 1981, FED PROC, V40, P2672
  • [3] AGING AND DIABETES
    ANDRES, R
    [J]. MEDICAL CLINICS OF NORTH AMERICA, 1971, 55 (04) : 835 - &
  • [4] CALCIUM, CELL-FUNCTION AND CELL-DEATH
    AVIOLI, LV
    [J]. AMERICAN JOURNAL OF NEPHROLOGY, 1986, 6 : 151 - 154
  • [5] Cellular ions in NIDDM: Relation of calcium to hyperglycemia and cardiac mass
    Barbagallo, M
    Gupta, RK
    Resnick, LM
    [J]. DIABETES CARE, 1996, 19 (12) : 1393 - 1398
  • [6] CELLULAR IONIC EFFECTS OF INSULIN IN NORMAL HUMAN ERYTHROCYTES - A NUCLEAR-MAGNETIC-RESONANCE STUDY
    BARBAGALLO, M
    GUPTA, RK
    RESNICK, LM
    [J]. DIABETOLOGIA, 1993, 36 (02) : 146 - 149
  • [7] Altered ionic effects of insulin in hypertension: Role of basal ion levels in determining cellular responsiveness
    Barbagallo, M
    Gupta, RK
    Bardicef, O
    Bardicef, M
    Resnick, LM
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (06) : 1761 - 1765
  • [8] BARBAGALLO M, 1996, ENDOCRINOLOGY VASCUL, P283
  • [9] Effects of chronic nimodipine on working memory of old rats in relation to defects in synaptosomal calcium homeostasis
    Batuecas, A
    Pereira, R
    Centeno, C
    Pulido, JA
    Hernández, M
    Bollati, A
    Bogonez, E
    Satrústegui, J
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 350 (2-3) : 141 - 150
  • [10] Borle A B, 1981, Rev Physiol Biochem Pharmacol, V90, P13