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Published on: December 5, 2017
Central choline suppresses plasma renin response to graded haemorrhage in rats
Naciye Isbil-Buyukcoskun1, Yesim O Ilcol, Mehmet Cansev
1Department of Physiology, Uludag University Medical School, Bursa, Turkey.
Insights
Central choline administration inhibits the renin-angiotensin system during hemorrhage, mediated by nicotinic receptors and vasopressin. This suggests a novel mechanism for blood pressure regulation involving choline.
Area of Science:
- Neuroscience
- Cardiovascular Physiology
- Pharmacology
Background:
- Central choline administration elevates blood pressure via vasopressin and catecholamines.
- The renin-angiotensin system is a key pressor system.
- The effect of choline on the renin-angiotensin pathway is unknown.
Purpose of the Study:
- To investigate the effect of central choline administration on the renin-angiotensin pathway during hemorrhage.
- To explore the involvement of nicotinic and muscarinic receptors, vasopressin, and catecholamines.
Main Methods:
- Rats received intracerebroventricular (i.c.v.) choline and were subjected to graded hemorrhage.
- Plasma renin activity (PRA), blood pressure, vasopressin, and catecholamines were measured.
- Receptor antagonists (mecamylamine, atropine) and a vasopressin antagonist were used.
Main Results:
- Central choline (i.c.v.) inhibited the increase in PRA during hemorrhage.
- Central choline increased blood pressure and enhanced vasopressin and catecholamine levels.
- The PRA inhibition was blocked by mecamylamine (nicotinic antagonist) but not atropine (muscarinic antagonist).
- A vasopressin antagonist reversed the PRA inhibition but not the blood pressure increase.
Conclusions:
- Central choline administration inhibits the plasma renin response to hemorrhage.
- This effect involves activation of nicotinic receptors and increased plasma vasopressin.
- Choline modulates cardiovascular regulation through multiple pressor systems.
Abstract:
Central administration of choline increases blood pressure in normotensive and hypotensive states by increasing plasma concentrations of vasopressin and catecholamines. We hypothesized that choline could also modulate the renin-angiotensin pathway, the third main pressor system in the body. Plasma renin activity (PRA), which serves as an index of the function of the peripheral renin-angiotensin system, was determined in rats subjected to graded haemorrhage following central choline administration. Intracerebroventricular (i.c.v.) injection of choline (12.5-150 microg), a precursor of the neurotransmitter acetylcholine (ACh), inhibited the increase in PRA in rats subjected to graded haemorrhage by sequential removal of 0.55 mL blood/100 g bodyweight. Choline, in the range 50-150 microg, increased blood pressure. Intraperitoneal (i.p.) administration of 150 microg choline failed to alter blood pressure and plasma renin responses to graded haemorrhage. Administration of a higher dose (90 mg/kg, i.p.) of choline decreased blood pressure and enhanced PRA in the first two blood samples obtained during the graded haemorrhage. Physostigmine (10 microg, i.c.v.), ACh (10 microg, i.c.v.), carbamylcholine (10 microg, i.c.v.) and cytidine 5'-diphosphocholine (CDP-choline; 250 microg, i.c.v.) increased blood pressure and attenuated plasma renin responses to graded haemorrhage. Inhibition of PRA by i.c.v. choline was abolished by i.c.v. pretreatment with mecamylamine (50 microg), but not atropine (10 microg). Blood pressure responses to choline (150 microg) were attenuated by pretreatment with both mecamylamine and atropine. Inhibition of PRA in response to central choline administration was associated with enhanced plasma vasopressin and catecholamine responses to graded haemorrhage. Pretreatment of rats with a vasopressin antagonist reversed central choline-induced inhibition of plasma renin responses to graded haemorrhage without altering the blood pressure response. In conclusion, central administration of choline inhibits the plasma renin response to graded haemorrhage. Nicotinic receptor activation and an increase in plasma vasopressin appear to be involved in this effect.
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