Key result
Hypoxia alters dopamine D2- and D1-receptor mRNA levels in the chemoreflex pathway organs of rabbits in an age-dependent and site-specific manner.
Hypoxia modulates dopamine receptor mRNA expression in the chemoreflex pathway differently depending on age and anatomical site in rabbits.
Answers are grounded in this paper and cite their sources.
Does not inform neonatal hypoxia management; hypothesis-generating for translational chemoreflex studies.
This study determined: (1) whether dopamine (DA) D2-receptor (R) and D1-R mRNA levels in the carotid body (CB), petrosal ganglion (PG) and superior cervical ganglion (SCG) are modulated by hypoxia; (2) the role of hypoxia intensity and exposure duration, and (3) whether the pattern of modulation differs between newborn (1-day-old) and adult rabbits. Rabbits were exposed to five FiO2 conditions: 21% (control); 15%/6 h; 15%/24 h; 8%/6 h and 8%/24 h. D2- and D1-R mRNA expression levels were calculated for each hypoxia condition relative to control using RT-PCR analysis. In the CB of 1-day-old rabbits, D2- and D1-R transcript levels increased and decreased after exposure to 15 and 8% O2, respectively. In the adult CB, D2- and D1-R transcript levels decreased independently of hypoxia intensities. Only changes in D1-R mRNA levels were dependent on exposure time. In the PG, both hypoxia intensities decreased the D2-R transcript levels in 1-day-old and adult rabbits; but for the D1-R mRNA levels, hypoxia decreased its level in 1-day-old rabbits and increased it in adults regardless of exposure duration. In the SCG, hypoxia had no determinant effect on the D2-R mRNA levels either in newborn or adult rabbits while it induced a decrease of D1-R transcript levels in 1-day-old rabbits and an increase in adult rabbits. It is concluded that hypoxia affects DA D2- or D1-R mRNA levels in the chemoreflex pathway in an age-dependent and site-specific manner.
No takes yet. Share an insight, caveat, or question.
Bairam et al. (2003) studied Hypoxia. Hypoxia vs. 21% O2 (control) was evaluated on Dopamine D2- and D1-receptor mRNA levels in the carotid body, petrosal ganglion, and superior cervical ganglion. Hypoxia alters dopamine D2- and D1-receptor mRNA levels in the chemoreflex pathway organs of rabbits in an age-dependent and site-specific manner.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: