The hypothalamic paraventricular nucleus and carotid receptors modulate hyperglycemia induced by hemorrhage

Brain Res. 2003 Dec 12;993(1-2):183-91. doi: 10.1016/j.brainres.2003.09.013.

Abstract

The aim of this study was to assess the role of cholinergic transmission in the paraventricular nucleus of the hypothalamus (PVN) and carotid body receptors in mediating a rise in plasma glucose levels in response to hemorrhagic hypotension in rats. Methylatropine (1x10(-9) mol) or 0.15 M NaCl (0.2 microl) was injected into the PVN of Wistar rats weighing 250-300 g bearing a chronic jugular catheter for blood sampling and hemorrhage (1.2 ml/100 g/2 min). Polyethylene cannulae (PE-10) were inserted into the left femoral artery for cardiovascular monitoring. In the other experimental protocol, hemorrhage was performed on rats submitted to bilateral carotid receptor denervation (H-CD). The results show that the hyperglycemic response to hemorrhage was decreased by either methylatropine (H-MA) treatment or bilateral carotid receptor denervation (10.3+/-0.4 mM, control, n=15 vs. 7.7+/-0.2 mM, H-MA, n=12, and 7.6+/-0.3 mM, H-CD, n=5, p<0.01). Furthermore, methylatropine did not affect the recovery of blood pressure after hemorrhage-induced hypotension, suggesting that the metabolic and pressor adjustments have different efferent pathways. Our data demonstrate that cholinergic input from the PVN and carotid receptors (chemo- and/or baroreceptors) might participate in the same neural pathway activated by hemorrhage-induced hypotension that produces hyperglycemia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atropine Derivatives
  • Blood Glucose / drug effects
  • Blood Pressure / drug effects
  • Carotid Arteries
  • Carotid Body / physiopathology*
  • Denervation / methods
  • Heart Rate / drug effects
  • Hemorrhage / chemically induced
  • Hemorrhage / complications*
  • Hyperglycemia / chemically induced
  • Hyperglycemia / etiology*
  • Male
  • Microinjections / methods
  • Models, Biological
  • Paraventricular Hypothalamic Nucleus / physiopathology
  • Rats
  • Rats, Wistar
  • Sodium Chloride / pharmacology
  • Statistics as Topic
  • Time Factors

Substances

  • Atropine Derivatives
  • Blood Glucose
  • Sodium Chloride
  • methylatropine