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Effect of Low-Frequency Renal Nerve Stimulation on Renal Glucose Release during Normoglycemia and a Hypoglycemic Clamp in Pigs.

Marius NistorMartin SchmidtCarsten M KlingnerCaroline KlingnerGeorg MatziolisSascha ShayganfarRené Schiffner
Published in: International journal of molecular sciences (2024)
Previously, we demonstrated that renal denervation in pigs reduces renal glucose release during a hypoglycemic episode. In this study we set out to examine changes in side-dependent renal net glucose release (SGN) through unilateral low-frequency stimulation (LFS) of the renal plexus with a pulse generator (2-5 Hz) during normoglycemia (60 min) and insulin-induced hypoglycemia ≤3.5 mmol/L (75 min) in seven pigs. The jugular vein, carotid artery, renal artery and vein, and both ureters were catheterized for measurement purposes, blood pressure management, and drug and fluid infusions. Para-aminohippurate (PAH) and inulin infusions were used to determine side-dependent renal plasma flow (SRP) and glomerular filtration rate (GFR). In a linear mixed model, LFS caused no change in SRP but decreased sodium excretion ( p < 0.0001), as well as decreasing GFR during hypoglycemia ( p = 0.0176). In a linear mixed model, only hypoglycemic conditions exerted significant effects on SGN ( p = 0.001), whereas LFS did not. In a Wilcoxon signed rank exact test, LFS significantly increased SGN ( p = 0.03125) and decreased sodium excretion ( p = 0.0017) and urinary flow rate ( p = 0.0129) when only considering the first instance LFS followed a preceding period of non-stimulation during normoglycemia. To conclude, this study represents, to our knowledge, the first description of an induction of renal gluconeogenesis by LFS.
Keyphrases
  • blood pressure
  • type diabetes
  • healthcare
  • ultrasound guided
  • high glucose
  • drug induced
  • adverse drug