Role of Calcium in Seizure Activity

Sophia Mian & Renuka Ramanathan

Background

Overview of Action Potential and Calcium's Role

Propagation of Action Potential at the Synaptic Cleft Influx of Calcium allows for nerve impulses to jump from one neuron to the next.

Neurons communicate at the chemical synapse. As an action potential, or nerve impulse, travels down the presynaptic axon, it activates voltage gated Calcium channels. The influx of Calcium causes synaptic vesicles to release neurotransmitters into the synaptic cleft. These neurotransmitters bind to receptors on the postsynaptic neuron allowing the action potential to continue along the next axon. The diagram to the right shows the steps of propagating an action potential from one neuron to another. Image is taken from Immune dysregulation and self-reactivity in schizophrenia: Do some cases of schizophrenia have an autoimmune basis? Jones et. al. Immunology and Cell Biology (2005)

Past Research

Previous research has included the use of novel seizure models such as the Xenopus laevis, or tadpole to characterize the effect of developmental seizures on critical processes which underly neural circuit formation and assess long term functional consequences.

Electrophysiology Recordings (EPR)

EPR enables us to study the electrical properties of cells by meausuring the voltage change due to electrical current flow. With respect to neurons, it allows researchers to directly measure the action potential activity. By attaching glass microelectrodes, researchers can obtain a readout of the voltage across a single neuron.

Two-Photon Calcium Microscopy

Two-Photon Calcium Imaging allows us to exploit calcium sensing methods in order to measure calcium levels in a cell. With respect to neurons, researchers will be able to analyze levels of calcium in a single cell and develop a connection between calcium and the action potential. By injecting a calcium sensitive dye and exciting this dye with a laser, researchers can analyze single cell responses to determine calcium levels.

Combined Technology Experimental Setup

Simultaneous electric potential and calcium spike measurements of single neurons will be obtained in a setup that combines EPR and TPM. The approach involves penetrating a neuron with a sharp glass electrode and using iontophoresis to inject the calcium dye - Fura-2. Fura-2 will be loaded into the neurons and the electrodes will create a current, causing like charges to repel. Thus, the direct current will drive, or pulse, Fura-2 into the neuron.

Research Proposal

•Currently, there is little information on the role of Calcium in a brain with seizure activity

•Studies have been done showing that a calcium spike is observe in neurons within a seizure model and also that these spikes are not seen in a brain exhibiting normal behavior

•Our goal is to further study the role of Calcium by investigating the influx of Calcium into the pre-synaptic terminal (i.e. is the voltage gated Calcium channel constitutively open?) over time.

•Our methods will include the use of a calcium indicator dye (the same as used in the Okhi article) and two photon microscopy to reveal the presence of Calcium

Methods

Part 1: Determining the Dose

Chemoconvulsant

Prior to beginning the main portion of our experiment, we will first need to determine the appropriate concentration (or more appropriately dose) of chemoconvulsant to use in a mouse model. Pentylenetetrazol (PTZ) is a commonly used chemoconvulsant in the literature. Hewapathirane et. al used 15 mM PTZ in order to induce a seizure in a Xenopus laevis tadpole. The first step in our protocol is to test a range of PTZ doses that will allow us to isolate a concentration that will give us behavior consistent with a seizure (this is characterized in the literature by excessive blinking of the eyes, myoclonic jerks, etc). Once we have agreed upon a concentration we can move to the actual experiment itself.

Part 2: Experimental Setup & Methods

Defining the Sample

In order to test the effects (if any) of two-photon calcium imaging on EPR and vice versa, we will need two populations of mice that serve as controls and one population of mice that will serve as the test samples for our experiment. Group 1 mice will only follow the methods outlined for EPR. Group 2 mice will only follow the methods outlined for two photon microscopy. Group 3 mice will be apart of an experimental setup that combines both EPR and calcium imaging simultaneously. Ideally, in order to obtain results which are reliable and comparable, these populations of mice can be anywhere from 10-50.

Protocol for Anesthetizing & Inducing Seizures

1. Anesthetize all three groups of mice. Possible anesthetics are ketamine/xylazine or urethane or alternatively, adult mice can be anesthetized by inhalation of isoflurane.
2. Perform EPR on Group 1, Two-Photon Calcium Imaging on Group 2, & the combined technologies approach on Group 3 in order to record baseline neuronal activity.
3. Paralyze mice (possibly with reversible paralytic agent pancuronium dibromide by injection)
4. In Group 1
5. Groups 2 and 3 – also load (directly into neurons) Fura-1, a calcium sensitive fluorescent indicator, in order to conduct two-photon calcium imaging
6. Inject all three groups with PTZ in order to induce seizure
   • Inject Fura-2, a calcium sensitive dye, into the neurons of Groups 2 & 3
7. Perform the three corresponding tests in order to record the seizure induced neuronal activity
8. Inject an anti-epileptic drug (possibly valproate) in order to stop seizures

Part 3: Assessing the Reliability of Combined Technologies Setup

We must now assess if by combining the EPR and TPM images, we have somehow induced or magnified the seizure. In order to do this we will conduct TUNEL live/dead cell assay on all three groups of mice. If we have not in any way affected the seizure with our methods and if we have regulated the dose of PTZ injected into all the mice, we expect to see on average the same amount of cell death in our controls as in our experimental group.

TUNEL Live/Dead Cell Assay

1. Determine size and area of slice to investigate
2. Fixation of tissue
   • Fixation stabilizes microscopic cellular structures and compositions in the specimens to allow them to withstand subsequent processing and to preserve them for retrospective analyses. The fixed cell and tissue specimens can also be used to extract biosynthetic molecules for biochemical or nucleotide sequence analysis. Without fixation, it would be difficult, if not impossible, to sensitively detect, localize, and quantitate biosynthetic or environmental molecules in many kinds of cell and tissue specimens.
3. Wash cells
4. Label cells with Br-dUTP
5. Rinse cells
6. Stain cells with Stain cells with fluorescein-PRB-1 (a fluorescein labeled anti BrdU monoclonal antibody)
7. Analyze via flow cytometry (also analyze a positive and negative control)

References

Two-photon Imaging of Synaptic Plasticity and Pathology in the Living Mouse Brain

Grutzendler et. al.

Two-photon microscopy is used to study the neuronal structure of animal models of neurodegeneration, brain injury and cerebrovascular disease

Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex

Ohki et. al.

Employ calcium sensing to reveal the micro-architecture in the visual cortex of the brains of rats and cats

In vivo imaging of seizure activity in a novel developmental seizure model

Hewapathirane et. al.

Characterize an in vivo model of seizures in Xenopus laevis tadpole – allowing direct examination of seizure activist and seizure induced effects on neuronal development