Xenon inhalation increases norepinephrine release from the anterior and posterior hypothalamus in rats

Citation
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
ISSN journal
0832610X → ACNP
Volume
48
Issue
7
Year of publication
2001
Pages
651 - 655
Database
ISI
SICI code
0832-610X(200107/08)48:7<651:XIINRF>2.0.ZU;2-F
Abstract
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.