DEVELOPMENTAL-CHANGES IN ISOLATED RAT TYPE-I CAROTID-BODY CELL K+ CURRENTS AND THEIR MODULATION BY HYPOXIA

Citation
Cj. Hatton et al., DEVELOPMENTAL-CHANGES IN ISOLATED RAT TYPE-I CAROTID-BODY CELL K+ CURRENTS AND THEIR MODULATION BY HYPOXIA, Journal of physiology, 501(1), 1997, pp. 49-58
Citations number
32
Categorie Soggetti
Physiology
Journal title
ISSN journal
00223751
Volume
501
Issue
1
Year of publication
1997
Pages
49 - 58
Database
ISI
SICI code
0022-3751(1997)501:1<49:DIIRTC>2.0.ZU;2-N
Abstract
1. Whole-cell patch-clamp recordings were used to investigate possible age-related changes in K+ currents of type I carotid body cells isola ted from the rat. K+ current density increased with age, as measured i n cells isolated from 4-day-old, 10-day-old and adult rats (greater th an or equal to 5 weeks old). 2. The proportion of current reversibly i nhibited by high [Mg2+] (6 mM), low [Ca2+] (0.1 mM) solutions, indicat ive of the proportion of current attributable to activation of Ca2+-se nsitive K+ (K-Ca) channels, was significantly smaller in cells of 4-da y-old rats compared with 10-day-old rats, despite inward Ca2+ current densities being similar in these two age groups. Inhibition of K+ curr ents by high [Mg2+], low [Ca2+] solutions was similar in 10-day-old an d adult type I cells. 3. Hypoxia (P-O2, 16-23 mmHg) caused reversible reductions in type I cells from rats of all age groups. However, reduc tions seen in cells of 4-day-old rats were significantly smaller than those seen in cells of 10-day-olds and adults. The degree of hypoxic i nhibition in these latter two groups was not significantly different. 4. In the presence of high [Mg2+], low [Ca2+] solutions, hypoxia (P-O2 16-23 mmHg) was without significant effect on residual K+ currents in cells from all age groups. 5. These observations indicate that K+ cur rent density increases with postnatal age in the rat. Between days 4 a nd 10, there appears to be a predominant enhancement of K-Ca channels, and over the same age range hypoxic sensitivity of K+ currents increa ses. Our findings demonstrate that this latter observation arises beca use hypoxia selectively inhibits K-Ca channels in cells at all ages st udied. These results suggest an important role for K-Ca channels in po stnatal maturation of hypoxic chemoreception in the rat carotid body.