Document Type
Article
Language
eng
Format of Original
7 p.
Publication Date
2004
Publisher
Elsevier
Source Publication
Neuroscience
Source ISSN
0306-4522
Original Item ID
doi: 10.1016/j.neuroscience.2003.10.020
Abstract
Exposure to 70% N2O evokes a robust antinociceptive effect in C57BL/6 (B6) but not in DBA/2 (D2) inbred mice. This study was conducted to identify quantitative trait loci (QTL) in the mouse genome that might determine responsiveness to N2O. Offspring from the F2 generation bred from B6 and D2 progenitors exhibited a broad range of responsiveness to N2O antinociception as determined by the acetic acid-induced abdominal constriction test. QTL analysis was then used to dissect this continuous trait distribution into component loci, and to map them to broad chromosomal regions. To this end, 24 spleens were collected from each of the following four groups: male and female F2 mice responding to 70% N2O in oxygen with 100% response (high-responders); and male and female F2 mice responding with 0% response (low-responders). Genomic DNA was extracted from the spleens and genotyped with simple sequence length polymorphism MapPairs markers. Findings were combined with findings from the earlier QTL analysis from BXD recombinant inbred mice [Brain Res 725 (1996) 23]. Combined results revealed two significant QTL that influence responsiveness to nitrous oxide on proximal chromosome 2 and distal chromosome 5, and one suggestive QTL on midchromosome 18. The chromosome 2 QTL was evident only in males. A significant interaction was found between a locus on chromosome 6 and another on chromosome 13 with a substantial effect on N2O antinociception.
Recommended Citation
Mueller, Janet L.; Ellenberger, E. A.; Vaughn, Linda K.; Belknap, John K.; and Quock, Raymond M., "Detection and Mapping of Quantitative Trait Loci that Determine Responsiveness" (2004). Biomedical Sciences Faculty Research and Publications. 80.
https://epublications.marquette.edu/biomedsci_fac/80
Comments
Accepted version. Neuroscience, Vol. 123, No. 3 (2004): 743-749. DOI. © 2004 Elsevier B.V. Used with permission.