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Chronic adrenergic receptor blockade does not prevent hyperinsulinemia-induced hypertension in rats

  • Henry L. Keen
    ,
  • Michael W. Brands(corresponding author)
    ,
  • Magdalena Alonso-Galicia
    ,
  • John E. Hall
*Corresponding author for this work
  • University of Mississippi
Scholary Output:
Contribution to journal
Article
Research
Peer-review

Abstract

Increased adrenergic activity has been suggested to mediate the hypertension associated with hyperinsulinemia. This study tested whether combined α1- and β-adrenergic receptor blockade would prevent insulin-induced hypertension when euglycemia was maintained by continuous intravenous glucose infusion. Sprague-Dawley rats (n = 16) were instrumented with artery and vein catheters and placed in metabolic cages. Propranolol and prazosin (10 mg/kg/day each) were infused continuously intravenously in 9 rats and 7 other rats received vehicle. Mean arterial pressure (MAP) and heart rate (HR) were measured 24 h per day using computerized methods. After a control period, a 7-day intravenous infusion of insulin (1.5 mU/kg/min) was begun and glucose was coadministered intravenously at 23 mg/kg/min to prevent hypoglycemia. The MAP averaged 93 ± 1 mm Hg in the blockade rats during the control period, which was significantly lower than the 98 ± 1 mm Hg in the normal rats. During insulin infusion, MAP increased similarly in both groups, with a 10 ± 2 mm Hg and 11 ± 1 mm Hg increase in normal and blockade rats, respectively, by day 7. The HR also increased in both groups: from 417 ± 8 beats/min to 426 ± 13 beats/min (P = NS) in normal rats and from 379 ± 10 beats/min to 419 ± 10 beats/min (P < .05) in blockade rats. Control sodium excretion averaged 2.5 ± 0.1 mEq/day in both groups and no significant change in sodium balance was measured in either group. All variables returned toward control after stopping insulin. These results suggest that increased adrenergic activity is not required for chronic hyperinsulinemia to raise blood pressure in rats.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Research
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 1192-1199 (8 pages)

Journal (Volume, Issue Number)

American journal of hypertension (Volume 9, Issue 12 I)

Publication milestones

  • Published - 12/1996

Publication status

Published - 12/1996

ISSN

0895-7061

Publication IDs

  • Scopus: 0030445126
  • PubMed: 8972890

Publication metrics

Metrics

SciVal
FWCI
1.24
SciVal
Author count
4
SciVal
citations
29
SciVal
Paper percentile
79
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1
Scopus
citations

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Citation count
31
Captures
7

Funding Details

Recewed February 26, 199b Accepted June 3, 1996 From the Department of Physiology and Biophysics, University of Mississipp~ Me&cal Center, Jackson, Misslssipp~ This research was supported by grants HL-39399, HL-23502, and HL-51971 from the National Institutes of Health. Address correspondence and reprint requests to Michael W. Brands, PhD, Department of Physiology and Biophysics, Umvers~ty of Mississippi Medical Center, 2500 North State Street, Jackson, MS 39216-4505.
FundersFunding numbers
Department of Physiology and Biophysics
-
University of Mississipp~ Me&cal Center
HL-51971, HL-23502
NIH
-
NHLBI
R01HL039399