Aug
12
Mon
2013
Invited Talk: Can we compute what we think? @ Amriteshwari Hall
Aug 12 @ 10:20 am – 10:51 am

gauteGaute Einevoll, Ph.D.
Professor of Physics, Department of Mathematical Sciences & Technology, Norwegian University of Life Sciences (UMB)


Multiscale modeling of cortical network activity: Key challenges

Gaute T. Einevoll Computational Neuroscience Group, Norwegian University of Life Sciences, 1432 Ås, Norway; Norwegian National Node of the International Neuroinformatics Coordinating Facility (INCF)

Several challenges must be met in the development of multiscale models of cortical network activity. In the presentation I will, based on ongoing work in our group (http://compneuro.umb.no/ ) on multiscale modeling of cortical columns, outline some of them. In particular,

  1. Combined modeling schemes for neuronal, glial and vascular dynamics [1,2],
  2. Development of sets of interconnected models describing system at different levels of biophysical detail [3-5],
  3. Multimodal modeling, i.e., how to model what you can measure [6-12],
  4. How to model when you don’t know all the parameters, and
  5. Development of neuroinformatics tools and routines to do simulations efficiently and accurately [13,14].

References:

  1. L. Øyehaug, I. Østby, C. Lloyd, S.W. Omholt, and G.T. Einevoll: Dependence of spontaneous neuronal firing and depolarisation block on astroglial membrane transport mechanisms, J Comput Neurosci 32, 147-165 (2012)
  2. I. Østby, L. Øyehaug, G.T. Einevoll, E. Nagelhus, E. Plahte, T. Zeuthen, C. Lloyd, O.P. Ottersen, and S.W. Omholt: Astrocytic mechanisms explaining neural-activity-induced shrinkage of extraneuronal space, PLoS Comp Biol 5, e1000272 (2009)
  3. T. Heiberg, B. Kriener, T. Tetzlaff, A. Casti, G.T. Einevoll, and H.E. Plesser: Firing-rate models can describe the dynamics of the retina-LGN connection, J Comput Neurosci (2013)
  4. T. Tetzlaff, M. Helias, G.T. Einevoll, and M. Diesmann: Decorrelation of neural-network activity by inhibitory feedback, PLoS Comp Biol 8, e10002596 (2012).
  5. E. Nordlie, T. Tetzlaff, and G.T. Einevoll: Rate dynamics of leaky integrate-and-fire neurons with strong synapses, Frontiers in Comput Neurosci 4, 149 (2010)
  6. G.T. Einevoll, F. Franke, E. Hagen, C. Pouzat, K.D. Harris: Towards reliable spike-train recording from thousands of neurons with multielectrodes, Current Opinion in Neurobiology 22, 11-17 (2012)
  7. H. Linden, T Tetzlaff, TC Potjans, KH Pettersen, S Grun, M Diesmann, GT Einevoll: Modeling the spatial reach of LFP, Neuron 72, 859-872 (2011).
  8. H. Linden, K.H. Pettersen, and G.T. Einevoll: Intrinsic dendritic filtering gives low-pass power spectra of local field potentials, J Computational Neurosci 29, 423-444 (2010)
  9. K.H. Pettersen and G.T. Einevoll: Amplitude variability and extracellular low-pass filtering of neuronal spikes, Biophysical Journal 94, 784-802 (2008).
  10. K.H. Pettersen, E. Hagen, and G.T. Einevoll: Estimation of population firing rates and current source densities from laminar electrode recordings, J Comput Neurosci 24, 291-313 (2008).
  11. K. Pettersen, A. Devor, I. Ulbert, A.M. Dale and G.T. Einevoll. Current-source density estimation based on inversion of electrostatic forward solution: Effects of finite extent of neuronal activity and conductivity discontinuities, Journal of Neuroscience Methods 154, 116-133 (2006).
  12. G.T. Einevoll, K. Pettersen, A. Devor, I. Ulbert, E. Halgren and A.M. Dale: Laminar Population Analysis: Estimating firing rates and evoked synaptic activity from multielectrode recordings in rat barrel cortex, Journal of Neurophysiology 97, 2174-2190 (2007).
  13. LFPy: A tool for simulation of extracellular potentials (http://compneuro.umb.no)
  14. E. Nordlie, M.-O. Gewaltig, H. E. Plesser: Towards reproducible descriptions of neuronal network models, PLoS Comp Biol 5, e1000456 (2009).

Gaute

Invited Talk: Modelling the syncytial organization and neural control of smooth muscle: insights into autonomic physiology and pharmacology @ Amriteshwari Hall
Aug 12 @ 12:20 pm – 12:43 pm

RohitRohit Manchanda, Ph.D.
Professor, Biomedical Engineering Group, IIT-Bombay, India


Modelling the syncytial organization and neural control of smooth muscle: insights into autonomic physiology and pharmacology

We have been studying computationally the syncytial organization and neural control of smooth muscle in order to help explain certain puzzling findings thrown up by experimental work. This relates in particular to electrical signals generated in smooth muscles, such as synaptic potentials and spikes, and how these are explicable only if three-dimensional syncytial biophysics are taken fully into account.  In this talk, I shall provide an illustration of outcomes and insights gleaned from such an approach. I shall first describe our work on the mammalian vas deferens, in which an analysis of the effects of syncytial coupling led us to conclude that the experimental effects of a presumptive gap junction uncoupler, heptanol, on synaptic potentials were incompatible with gap junctional block and could best be explained by a heptanol-induced inhibition of neurotransmitter release, thus compelling a reinterpretation of the mechanism of action of this agent.  I shall outline the various lines of evidence, based on indices of syncytial function, that we adduced in order to reach this conclusion. We have now moved on to our current focus on urinary bladder biophysics, where the questions we aim to address are to do with mechanisms of spike generation. Smooth muscle cells in the bladder exhibit spontaneous spiking and spikes occur in a variety of distinct shapes, making their generation problematic to explain. We believe that the variety in shapes may owe less to intrinsic differences in spike mechanism (i.e., in the complement of ion channels participating in spike production) and more to features imposed by syncytial biophysics. We focus especially on the modulation of spike shape in a 3-D coupled network by such factors as innervation pattern, propagation in a syncytium, electrically finite bundles within and between which the spikes spread, and some degree of pacemaker activity by a sub-population of the cells. I shall report two streams of work that we have done, and the tentative conclusions these have enabled us to reach: (a) using the NEURON environment, to construct the smooth muscle syncytium and endow it with synaptic drive, and (b) using signal-processing approaches, towards sorting and classifying the experimentally recorded spikes.

Rohit (1) Rohit (2)

Aug
13
Tue
2013
Invited Talk: Gut microbiome and health- Moving towards the new era of translational medicine @ Acharya Hall
Aug 13 @ 1:30 pm – 1:50 pm

SharmilaSharmila Mande, Ph.D.
Principal Scientist and Head, Bio Sciences R&D, TCS Innovation Labs, Pune


Gut microbiome and health: Moving towards the new era of translational medicine

The microbes inhabiting our body outnumber our own cells by a factor of 10. The genomes of these microbes, called the ‘second genome’ are therefore expected to have great influence on our health and well being. The emerging field of metagenomics is rapidly becoming the method of choice for studying the microbial community (called microbiomes) present in various parts of the human body. Recent studies have implicated the role of gut microbiomes in several diseases and disorders. Studies have indicated gut microbiome’s role in nutrient absorption, immuno-modulation motor-response, and other key physiological processes. However, our understanding of the role of gut microbiota in malnutrition is currently incomplete. Exploration of these aspects are likely to help in understanding the microbial basis for several physiological disorders associated with malnutrition (eg, increased susceptibility to diarrhoeal pathogens) and may finally aid in devising appropriate probiotic strategies addressing this menace. A metagenomic approach was employed for analysing the differences between gut microbial communities obtained from malnourished and healthy children. Results of the analysis using TCS’ ‘Metagenomic Analysis Platform’ were discussed in detail during my talk.