Cerebrospinal fluid sodium concentration and osmosensitive sites related to arterial pressure in anaesthetized rats

Pflügers Archiv - Tập 431 - Trang 807-813 - 1996
Munetaka Hirose1, Hiroshi Nose2, Mian Chen2, Takiko Yawata2
1Department of Anaesthesiology, Kyoto Prefectural University of Medicine, Kawaramachi, Kamigyoku, Japan
2Department of Physiology, Kyoto Prefectural University of Medicine, Kyoto Japan

Tóm tắt

Intracerebroventricular injection of hypertonic saline induces experimental hypertension. To measure [Na] in the vicinity of osmosensitive sites, we continuously measured [Na] in cerebrospinal fluid ([Na]csf) in the lateral ventricle (LV, n = 6), in the third ventricle (V3, n = 6) and in the medial preoptic nucleus (MPO, n = 6) ([Na]MPO) with a Na-sensitive electrode together with mean arterial pressure (MAP) during infusion of hypertonic artificial cerebrospinal fluid (ACSF, [Na] = 1,000 meq/kg H2O) at 5 µl/min for 3 min into the LV in urethane-anaesthetized rats. [Na]csf in the LV began to increase at the beginning of infusion, reaching a peak of 48 ± 9 meq/kg H2O (mean ± SE) around the end of infusion, then recovering to the pre-infusion level by 17 min. [Na]csf in V3 changed similarly to that in the LV without any delay, although the peak value was reduced (61% , P < 0.05). In the MPO, in contrast the increase in [Na]MPO was delayed (3 min, P < 0.002) and the peak reduced even further (to 37%, P < 0.01) compared with that in V3. Thereafter, it remained higher than the pre-infusion level until the end of recovery (P < 0.05). MAP began to increase at the onset of infusion (P < 0.05); the maximum increase of 16 ± 2 mm Hg (n = 18) was reached at the end of infusion, whereafter this level was almost sustained until the end of the 22-min recovery period. To analyse quantitatively the relationship between MAP and [Na]csf, hypertonic ACSF was infused at 2.5 µl/min into the LV. [Na]csf in the LV and MAP increased at half the rates seen with 5 µl/min. These results suggest that the first increase in MAP after hypertonic infusion into the LV is due to the increase in [Na] in the LV and V3, and that the subsequent sustained increase in MAP is related to the delayed increase in [Na] in the periventricular tissues of the V3.

Tài liệu tham khảo

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