Key result
Intravenous infusion of angiotensin III and physiological stimuli altered plasma angiotensin II levels but did not change CSF levels, indicating it does not cross the blood-CSF barrier.
The central nervous renin-angiotensin system appears to be regulated independently of the peripheral system in dogs.
Central RAS may be independently regulated in this model; leaves open linkage to peripheral control in human hypertension.
What regulates the activity of the central nervous renin-angiotensin system is not known. To define whether control of this central system is linked to that in the periphery, simultaneous blood and cerebrospinal fluid (CSF) samples for measurement of immunoreactive angiotensin II were drawn from anesthetized dogs during hemorrhage, furosemide-induced volume depletion, insulin-hypoglycemia, beta-adrenergic blockade and saline infusion. Despite vigorous increments or decrements in plasma innunoreactive angiotensin II, CSF levels remained stable. Since immunoreactive angiotensin II in dog CSF is claimed to be mainly the heptapeptide des-Asp1-angiotensin II (angiotensin III), the possibility that the level of this peptide within CSF simply reflects plasma concentrations was assessed by infusing angiotensin III (2.5 and 25 ng/kg/min intravenously, each for 60 minutes) and monitoring plasma and CSF peptide levels. Whereas plasma immunoreactive angiotensin II levels increased appropriately across the infusions, no change in CSF levels was observed. These studies indicate the angiotensin III does not cross the blood-CSF barrier, at least in the short term.
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M. Gary Nicholls (1979) studied this question. Angiotensin III infusion and physiological stimuli was evaluated on Cerebrospinal fluid levels of immunoreactive angiotensin II. Intravenous infusion of angiotensin III and physiological stimuli altered plasma angiotensin II levels but did not change CSF levels, indicating it does not cross the blood-CSF barrier.
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