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Chronic insulin administration elevates blood pressure in rats
W P Meehan1, T A Buchanan, W Hsueh
1Department of Medicine, University of Southern California Medical School, Los Angeles.
Hypertension (Dallas, Tex. : 1979)
|June 1, 1994
Summary
Infused insulin significantly increases blood pressure in rats more than dietary glucose alone. Clonidine, a sympatholytic agent, effectively prevented these insulin-induced blood pressure and heart rate elevations.
Area of Science:
- Cardiovascular Physiology
- Endocrinology
Background:
- Elevated blood pressure is a significant health concern.
- The roles of dietary glucose and insulin in blood pressure regulation require further elucidation.
Purpose of the Study:
- To investigate the independent and combined effects of dietary glucose and exogenous insulin on blood pressure and heart rate in a rat model.
- To assess the impact of a sympatholytic agent on insulin-induced cardiovascular changes.
Main Methods:
- Male Sprague-Dawley rats were subjected to a crossover design, receiving either a 4% glucose supplement or a combination of glucose and insulin infusion.
- Blood pressure and heart rate were monitored using radio telemetry.
- Blood samples were analyzed for glucose and insulin levels.
- The effect of clonidine was evaluated in rats receiving glucose and insulin.
Main Results:
- Both dietary glucose and insulin infusion increased blood pressure, with insulin infusion causing a more pronounced and rapid rise.
- Plasma insulin levels were positively correlated with blood pressure changes.
- Heart rate increased similarly during both glucose and insulin treatments.
- Clonidine administration attenuated the rise in blood pressure and heart rate.
Conclusions:
- Exogenous insulin plays a significant role in elevating blood pressure, potentially exceeding the effect of dietary glucose alone.
- Insulin-induced hypertension may be mediated through sympathetic pathways, as evidenced by clonidine's efficacy.
- These findings highlight the complex interplay between glucose metabolism, insulin, and cardiovascular regulation.