H. Yoshida et al., Xenon inhalation increases norepinephrine release from the anterior and posterior hypothalamus in rats, CAN J ANAES, 48(7), 2001, pp. 651-655
Citations number
19
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Journal title
CANADIAN JOURNAL OF ANAESTHESIA-JOURNAL CANADIEN D ANESTHESIE
Purpose: To investigate the effect of xenon (Xe) and nitrous oxide (N2O) on
norepinephrinergic neuronal activity in the rat medial preoptic area (mPOA
) and posterior hypothalamus (PH) using microdialysis.
Methods: Sixty male Wistar rats were equally allocated to two groups: mPOA
and PH, A microdialysis probe was implanted into the mPOA or the PH. In bot
h groups, each animal was exposed to one of the following inhalations: 25%
oxygen (control, n = 6 ), 30% Xe (n = 6), 60% Xe (n = 6), 30% N2O (n = 6) o
r 60% N2O (n = 6). Norepinephrine concentration in the perfused artificial
cerebrospinal fluid was measured by high pressure liquid chromatography at
ten-minute intervals. After plotting the time-norepinephrine concentration
curve, the area under the curve (AUC) in each group was calculated.
Results: In the mPOA, 30 and 60% Xe, but only 60% N2O significantly increas
ed norepinephrine release. The AUC in the 30% Xe, 60% Xe or 60% N2O group w
as 160 +/- 9 (P < 0.05), 288 +/- 42 (P < 0.01) or 237 +/- 46 pg(.)min/sampl
e (P < 0.01), respectively, compared to that in the control group: 77 +/- 1
4 pg(.)min/sample. In the PH, only 60% Xe significantly increased norepinep
hrine release compared to control (AUC: 191 +/- 38 vs 71 +/- 1 pg(.)min/sam
ple, P < 0.01).
Conclusion: The present data suggest that Xe stimulates norepinephrinergic
neurons more potently than N2O; 1.2 times more in the mPOA and 2.5 times mo
re in the PH. This stimulant effect may contribute to the hypnotic and symp
athotonic effects of Xe in rats.