This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The adverse experiences related to preterm birth are associated with cognitive and behavioral defects in ex-preterm children, indicating disruption of the cortex, the primary brain region involved in aptitude and intelligence. Nevertheless, it has not been established that premature infants experience pain or neural consequences from pain, nor is it known if the benefits of anesthetic drugs outweigh disadvantages in this age group. The overall goals of this project are to understand how pain and/or anesthesia in newborns affects the manner in which brain architecture develops, matures, and ages, with a focus on the cortex, and the role of group of a cells critically involved in normal cortical development, the subplate neurons. We hypothesize that when perinatal mammals are exposed to repetitive pain or prolonged anesthesia, cortical organization is irreparably altered, a disruption that can be minimized if anesthesia is administered for an appropriate time period. Because rats exposed to repetitive neonatal pain and/or anesthesia develop deficits mimicking those of ex-preterm children, we propose to characterize the cortex of rodents that have undergone adverse perinatal experiences with and without anesthetic drugs. Utilizing cellular labeling techniques, and correlated light and fluorescent microscopy, we will compare the structure of the cortex, including subplate neurons, between treated and control animals across development. Using bioinfomatic techniques, we will generate predictions for appropriate anesthetic intervals in experimental animals. Using these data, we will begin to understand how cortical disruption may be implicated in developmental disorders associated with ex-preterm children. It is expected that this research will demonstrate to students the potential of careers in biomedical research, as well as support federal funding for undergraduate research experiences, and ultimately lead to the development of proposals for federal funds to continue to investigate in detail how disruption of the cortex may be evidenced in developmental disorders.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
2P20RR016460-09
Application #
8168090
Study Section
Special Emphasis Panel (ZRR1-RI-7 (01))
Project Start
2010-05-19
Project End
2011-04-30
Budget Start
2010-05-19
Budget End
2011-04-30
Support Year
9
Fiscal Year
2010
Total Cost
$119,292
Indirect Cost
Name
University of Arkansas for Medical Sciences
Department
Physiology
Type
Schools of Medicine
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
Doyle, Erin L; Fillman, Christy L; Reyna, Nathan S et al. (2018) Genome Sequences of Four Cluster P Mycobacteriophages. Genome Announc 6:
McSweeney, Jean C; Hudson, Teresa J; Prince, Latrina et al. (2018) Impact of the INBRE summer student mentored research program on undergraduate students in Arkansas. Adv Physiol Educ 42:123-129
Wolyniak, Michael J; Reyna, Nathan S; Plymale, Ruth et al. (2018) Mass Spectrometry as a Tool to Enhance ""-omics"" Education. J Microbiol Biol Educ 19:
Musa, Aliyu; Ghoraie, Laleh Soltan; Zhang, Shu-Dong et al. (2018) A review of connectivity map and computational approaches in pharmacogenomics. Brief Bioinform 19:506-523
Caviness, Perry; Bauer, Ryan; Tanaka, Keisuke et al. (2018) Ca2+ -induced orientation of tandem collagen binding domains from clostridial collagenase ColG permits two opposing functions of collagen fibril formation and retardation. FEBS J 285:3254-3269
Hill, Brent J F; Dalton, Robin J; Joseph, Biny K et al. (2017) 17?-estradiol reduces Cav 1.2 channel abundance and attenuates Ca2+ -dependent contractions in coronary arteries. Pharmacol Res Perspect 5:
Allison, Devin; Delancey, Evan; Ramey, Hunter et al. (2017) Synthesis and antimicrobial studies of novel derivatives of 4-(4-formyl-3-phenyl-1H-pyrazol-1-yl)benzoic acid as potent anti-Acinetobacter baumannii agents. Bioorg Med Chem Lett 27:387-392
MacNicol, Melanie C; Cragle, Chad E; McDaniel, F Kennedy et al. (2017) Evasion of regulatory phosphorylation by an alternatively spliced isoform of Musashi2. Sci Rep 7:11503
Gao, Bo; Li, Guojun; Liu, Juntao et al. (2017) Identification of driver modules in pan-cancer via coordinating coverage and exclusivity. Oncotarget 8:36115-36126
Rahmatallah, Yasir; Zybailov, Boris; Emmert-Streib, Frank et al. (2017) GSAR: Bioconductor package for Gene Set analysis in R. BMC Bioinformatics 18:61

Showing the most recent 10 out of 234 publications