Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
Abstracts - Association for Chemoreception Sciences
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P O S T E R S<br />
#P99 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
Chloride Homeostatsis in Trigeminal Sensory Neurons<br />
Debbie Radtke 1 , Nicole Schöbel 1 , Jennifer Spehr 2 , Hanns Hatt 1<br />
1<br />
Ruhr-University Bochum, Department of Cell Physiology<br />
Bochum, Germany, 2 RWTH-Aachen University, Institute <strong>for</strong><br />
Biology II Aachen, Germany<br />
The trigeminal system is known to play an important role in<br />
chemo- and thermosensation as well as the perception of pain.<br />
Recent studies have shown a connection between intracellular<br />
chloride accumulation and pain perception by neurons of the<br />
dorsal root ganglia (DRG), but little is known about the chloride<br />
homeostasis in TG neurons. The intracellular chloride<br />
concentration is mainly controlled by cation-coupled chloride<br />
cotransporters. The Na + K + 2Cl - cotransporter NKCC1<br />
accumulates Cl - intracellularly and is highly expressed in<br />
embryonal neurons of the central nervous system. During late<br />
embryonal to early postnatal development NKCC1 is<br />
downregulated accompanied by an upregulation of Cl - -extruding<br />
cotransporters. Due to this “chloride switch” opening of Cl -<br />
conductances leads to hyperpolarization of adult central neurons.<br />
However, some peripheral neurons like olfactory sensory neurons<br />
and neurons of the DRG maintain high intracellular Cl - levels<br />
even in adulthood resulting in cellular depolarization after<br />
opening of Cl - conductances. Here, we show that isolated neurons<br />
of wild type (WT) mice display robust Ca 2+ transients upon<br />
GABA stimulation in Ca 2+ -imaging experiments. In neurons of<br />
NKCC1 -/- mice, however, these responses are dramatically<br />
diminished with respect to the number of responsive cells and<br />
signal amplitude. Furthermore, we use the chloride imaging<br />
technique to investigate changes of intracellular Cl - levels upon<br />
GABA stimulation of TG neurons of WT and NKCC1 -/- mice.<br />
Additionally, we determine the intracellular Cl - concentration of<br />
neurons of both WT and NKCC1 -/- mice using the doubleionophor<br />
technique. We conclude that NKCC1 is the main Cl -<br />
accumulating transporter in TG neurons. Further investigations<br />
aim at clarifying the role of NKCC1 in connection with<br />
trigeminal pain perception.<br />
#P100 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
Pain Processing Networks Revealed Using Fully Exploratory<br />
Analysis: An FMRI Study Using Trigeminal Stimulation<br />
Martin Wiesmann 1,2 , Veronika Schoepf 2,3,4 , Christian<br />
Windischberger 3,4 , Christian H Kasess 3,5 , Jessica Albrecht 2,6 ,<br />
Rainer Kopietz 2 , Anna Maria Kleemann 2 , Ewald Moser 3,4<br />
1<br />
Dept. of Neuroradiology, Technical University of Aachen<br />
RWTH Aachen, Germany, 2 Dept. of Neuroradiology, Ludwig-<br />
Maximilian-University Munich Munich, Germany, 3 MR Centre of<br />
Excellence, Medical University Vienna Vienna, Austria, 4 Centre<br />
<strong>for</strong> Medical Physics and Biomedical Engineering, Medical<br />
University Vienna Vienna, Austria, 5 Division of Biological<br />
Psychiatry, Dept. of Psychiatry and Psychotherapy, Medical<br />
University Vienna Vienna, Austria, 6 Monell Chemical Senses<br />
Center Philadelphia, PA, USA<br />
Fully Exploratory Network Independent Component Analysis<br />
(FENICA) on functional MRI data is based on the assumption<br />
that group networks develop on the basis of spatially consistent<br />
single-subject components. The analyzing method introduced in<br />
this study includes two different processing stages. First<br />
Independent Component Analysis (ICA) on a single-subject level<br />
is conducted and the second step includes analysis based crosscorrelating<br />
the derived single-subject components. The most<br />
important aspect of this exploratory method without the need <strong>for</strong><br />
a priori definition of the applied stimulus time course or the<br />
specification of a template including expected regions of interest is<br />
the single-subject character the method is based on. To test this<br />
new method a trigeminal stimulation experiment was per<strong>for</strong>med.<br />
It is known that the processing of intranasal CO2 stimuli evokes<br />
specific activation involving a part of the general pain processing<br />
network. Functional images were obtained from 22 healthy<br />
volunteers using a 3T MRI scanner. We used an intranasal CO2<br />
event-related birhinal stimulation paradigm. Image preprocessing<br />
was per<strong>for</strong>med using SPM5. For further artefact corrections two<br />
regions of interests (white matter and ventricles) were defined and<br />
time courses were extracted and regressed out <strong>for</strong> each singlesubject.<br />
Single-subject ICA was per<strong>for</strong>med using probabilistic<br />
ICA as implemented in FSL. Group analysis with FENICA<br />
revealed areas known to be specifically activated <strong>for</strong> the<br />
processing of intranasal trigeminal stimulation and was able to<br />
clearly obtain the network involved in the processing of olfactory<br />
trigeminal stimulus processing. We can conclude that FENICA<br />
provides a truly exploratory, data-driven, operator independent<br />
and there<strong>for</strong>e unbiased way of assessing trigeminal networks.<br />
#P101 POSTER SESSION II:<br />
OLFACTORY PHYSIOLOGY & CELL BIOLOGY;<br />
TASTE MOLECULAR GENETICS;<br />
CHEMESTHESIS & TRIGEMINAL<br />
Real-time PCR of trigeminal receptor mRNAs in human<br />
nasal biopsies<br />
Jacqueline Zimmermann 1,2 , Thomas Hummel 2 , Andreas<br />
Hermann 3 , Alexander Storch 3 , Sylvia Kanzler 3 , Mandy Scheibe 2 ,<br />
Martin Witt 4<br />
1<br />
Dept. Anatomy,TU Dresden Dresden, Germany,<br />
2<br />
Otorhinolaryngology, TU Dresden Dresden, Germany, 3 Dept.<br />
Neurology and Center <strong>for</strong> Regenerative Therapies Dresden<br />
(CRTD), TU Dresden Dresden, Germany, 4 Dept. Neurology<br />
and Center <strong>for</strong> Regenerative Therapies Dresden (CRTD), TU<br />
Dresden Dresden, Germany, 5 Dept. Neurology and Center <strong>for</strong><br />
Regenerative Therapies Dresden (CRTD), TU Dresden Dresden,<br />
Germany, 6 Otorhinolaryngology, TU Dresden Dresden, Germany,<br />
7<br />
University of Rostock Rostock, Germany<br />
Background: Previous research suggests that chemosensory<br />
stimuli mediated by branches of the trigeminal nerve are perceived<br />
differentially dependent on the location within the nasal cavity.<br />
Aim: The aim of this study was to acquire data on the occurrence<br />
of various trigeminal receptor mRNAs in different locations of<br />
the nasal mucosa using real-time PCR. Subjects & Methods:<br />
Biopsies of 12 healthy individuals (mean age: 37.8 years) were<br />
taken from the insertions of the middle and inferior turbinates, as<br />
well as anterior ventral and posterior dorsal septum. Real time-<br />
PCR was per<strong>for</strong>med using primers <strong>for</strong> TRPA1 (ankyrin-like<br />
receptor with transmembrane domain I), ACCN3 (acid-sensing<br />
ion channel), TRPV1 (transient receptor potential vanilloid<br />
receptor 1), TRPM8 (transient receptor potential receptor M8),<br />
and CALCB1 (calcitonin gene-related product). As housekeeping<br />
60 | AChemS <strong>Abstracts</strong> 2010 <strong>Abstracts</strong> are printed as submitted by the author(s)