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High-resolution measurements of middle ear gas volume changes in the rabbit enables estimation of its mucosal CO(2) conductance.

ABSTRACT: Transmucosal CO(2) exchange in the middle ear (ME) of the New Zealand White rabbit (Oryctolagus cuniculus) was studied using an accurate novel detecting and recording system for measuring gas volume changes at constant pressure, based on a principle that was previously used by Kania et al. (Acta Otolaryngol 124:408-410, 2004). After the ME cavity was washed with ambient air, the initial diffusion rate of CO(2) (V(.-)(i)CO(2)) from the blood perfusing the ME mucosa was calculated from gas volume change measurements. In nine cases, the (V(.-)(i)CO(2))calculated after normalization due to shifts in baseline was 314+/-112 microL x h(-1) (mean +/- SD). In two cases where normalization was not needed, (V(.-)(i)CO(2)) was 409 microL x h(-1) (276 and 543 microL x h(-1)). Normalization of (V(.-)(i)CO(2)) data was also made in five additional cases where secretion of fluids from the lining of the ear canal was observed. In these cases (V(.-)(i)CO(2)) was 245 +/- 142 microL x h(-1). No differences were found between results obtained in the three groups. Thus, an overall mean value of (V(.-)(i)CO(2)) of 305 +/- 131 microL x h(-1) (n = 16) was calculated. An effective coefficient of conductance of CO(2) (G(CO(2))) between the mucosal circulation and the ME gas cavity of the New Zealand White rabbit was estimated to be approximately 0.05 microL (h x Pa)(-1) and compared to the G(CO(2)) estimated for humans in a different study.

SUBMITTER: Marcusohn Y

PROVIDER: S-EPMC2504611 | biostudies-other | 2006 Sep

REPOSITORIES: biostudies-other

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Project description:Objective: Otitis media is known to alter expression of cytokine and other genes in the mouse middle ear and inner ear. However, whole mouse genome studies of gene expression in otitis media have not previously been undertaken. Ninety-nine percent of mouse genes are shared in the human, so these studies are relevant to the human condition. Methods: To assess inflammation-driven processes in the mouse ear, gene chip analyses were conducted on mice treated with trans-tympanic heat-killed Hemophilus influenza using untreated mice as controls. Middle and inner ear tissues were separately harvested at 6 hours, RNA extracted, and samples for each treatment processed on the Affymetrix 430 2.0 Gene Chip for expression of its 34,000 genes. Results: Statistical analysis of gene expression compared to control mice showed significant alteration of gene expression in 2,355 genes, 11% of the genes tested and 8% of the mouse genome. Significant middle and inner ear upregulation (fold change >1.5, p<0.05) was seen in 1,081 and 599 genes respectively. Significant middle and inner ear downregulation (fold change <0.67, p<0.05) was seen in 978 and 287 genes respectively. While otitis media is widely believed to be an exclusively middle ear process with little impact on the inner ear, the inner ear changes noted in this study were numerous and discrete from the middle ear responses. This suggests that the inner ear does indeed respond to otitis media and that its response is a distinctive process. Numerous new genes, previously not studied, are found to be affected by inflammation in the ear. Conclusion: Whole genome analysis via gene chip allows simultaneous examination of expression of hundreds of gene families influenced by inflammation in the middle ear. Discovery of new gene families affected by inflammation may lead to new approaches to the study and treatment of otitis media. There are 8 control samples and 9 samples trans-tympanically injected with H flu 10e9 for 6 hours. Each sample is from a single animal.

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High-resolution measurements of middle ear gas volume changes in the rabbit enables estimation of its mucosal CO(2) conductance.

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