- A Nautilus has 90 tentacles. (Jennifer Basil and R. Crook)
- The vertical lobe system of cephalopod brain resembles mammalian cortex. The axons of median superior frontal lobe neurons project to the small amacrine interneurons en passant. (Binyamin Hochner et al.)
- Oral veil has peripheral ganglia. They are bilaterally independent. Small 5-HT cells near MCC project there. (Rhanor Gillette)
- cAMP produces persistant Na current that plays a role in long-term memory in Lymnea. (George Kemenes)
- Ca-activated PKC activates AC in B51 in operant conditioning. (Jack Byrne)
- Intermediate-term potentiation involves postsynaptic Ca signal. (David Glanzman)
- Homosynaptic depression of Aplysia sensory-motor synapse is caused by decrease in the number of release sites and the reduction of release per varicosity. (Guy Malkinson and Micha Spira)
- Spontaneous transmitter release from the presynaptic neuron is both necessary and sufficient to recruit postsynaptic mechanisms of intermediate- and long-term synaptic plasticity in Aplysia. (Robert Hawkins)
- Injured axon produce afterdischarge in response to a train of stimuli. Some primitive plasticity signals in addition to Ca2+. (Edgar Walters)
- Bitter solution works very well for land slug learning. (Ryota Matsuo)
- Reversal of synapse from inhibitory to excitatory after formation of soma-to-soma synapse of Lymnaea neurons by appearance of nAChR. RTK inhibitor, Lavendustin A. (Fenglian Xu)
- Reversal of microtubules occurs when axon is transected. Awesome movies of microtubule formation and axonal transport. (Micha Spira)
- PKC-19-31 blocks homosynaptic depression. Burst-dependent protection of depression... Is this really preventing the depression or simply causing an overriding facilitation? (Tom Abrams)
- Translocation of PKC can be visualized. PKA downregulates PKC in Aplysia sensory neurons. (Wayne Sossin)
- Single action potential can terminate PTP. (Naweed Syed)
- In octopus, each sucker has its own ganglion. A sucker can pinch a string. Nice arm-sucker co-ordination. (Frank Grasso)
- Something mediates semi-sinchronous activity of left and right B67. (Mark Miller)
- The amplitude of EPSP evoked by B21 is determined not only by the degree of AP propagation, but also some nifedipine-sensitive Ca influx. (Betsy Cropper)
- There are five 5-HT cells in early laval state of molluscs. (Roger Croll)
- There is cut-end accumulation of FMRF-amide. (Ferdinand Vilim)
- Delayed rectifier type K channels form clusters near soma. PKC activation recruites Ca channels to the membrane at the terminals. (Leonard Kaczmarek)
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Sunday, February 15, 2009
Saturday, February 14, 2009
Molluscan neuroscience meeting
I am attending the molluscan neuroscience meeting in Old San Juan, Puerto Rico.
This meeting can be one of the best meetings I ever attended.
So many good talks. Many big-name people. Beautiful data and movies by highly advanced techniques.
It is great to meet some of my SfN friends again. Especially on a dispatched island in Caribbean ocean.
This whole meeting is like a field trip.
The open discussion made by Drs. Hawkins, Glanzman, Abrams and Byrne and others was terrific. I had never seen anything like that, although the topic they were discussing over and over did not sound that much important to me.
Having a field trip to the beach was also good. Seeing those smart people wearing WalMart-like bathing suits is kinda rare experience.
Only thing I regret to death was that I forgot to credit Drs. Russell Wyeth and Owen Woodward for their beautiful Tritonia swimming movie I used in my talk. Russel has many good Tritonia movies.
http://people.stfx.ca/rwyeth/vidsimages.html
This meeting can be one of the best meetings I ever attended.
So many good talks. Many big-name people. Beautiful data and movies by highly advanced techniques.
It is great to meet some of my SfN friends again. Especially on a dispatched island in Caribbean ocean.
This whole meeting is like a field trip.
The open discussion made by Drs. Hawkins, Glanzman, Abrams and Byrne and others was terrific. I had never seen anything like that, although the topic they were discussing over and over did not sound that much important to me.
Having a field trip to the beach was also good. Seeing those smart people wearing WalMart-like bathing suits is kinda rare experience.
Only thing I regret to death was that I forgot to credit Drs. Russell Wyeth and Owen Woodward for their beautiful Tritonia swimming movie I used in my talk. Russel has many good Tritonia movies.
http://people.stfx.ca/rwyeth/vidsimages.html
Friday, February 13, 2009
Giving a talk
I gave a talk yesterday. I think it went very well. Paul seemed happy with it. I received many good comments.
I am usually not good at giving a speech. I often get choked even when I present my data in our weekly lab meeting. This is not because of English. I am not good at giving a speech even in Japanese.
However, sometimes I feel very comfortable standing on a big stage. This happened yesterday. I didn't want to finish my talk. I felt like to talk about my stuff forever. I don't know why. I even remember that a mosquito was flying in front of the screen. I kinda enjoyed watching it while talking about heterosynaptic plasticity. I wish this happens every time I give a talk.
I am usually not good at giving a speech. I often get choked even when I present my data in our weekly lab meeting. This is not because of English. I am not good at giving a speech even in Japanese.
However, sometimes I feel very comfortable standing on a big stage. This happened yesterday. I didn't want to finish my talk. I felt like to talk about my stuff forever. I don't know why. I even remember that a mosquito was flying in front of the screen. I kinda enjoyed watching it while talking about heterosynaptic plasticity. I wish this happens every time I give a talk.
Wednesday, January 14, 2009
What so good about being a researcher is...
Saturday, January 10, 2009
My latest paper published
My paper, "State-, Timing-, and Pattern-Dependent Neuromodulation of Synaptic Strength by a Serotonergic Interneuron" with Paul Katz is out in the Journal of Neuroscience.
By studying sea slug's brain, we described that the strength of synaptic transmission is controled by its own activity level and by a neuromodulatory input. These two types of synaptic plasticity interact with each other to produce complex and dynamic changes in the strength of the synapse. Such changes may play important roles in configuration of neural circuit to produce specific motor outputs.
Although the development of techniques using brain slice preparations had made a great advance in our knowledge of synaptic plasticity, I am hoping that this paper shows that researches in invertebrate neuroscience are still front runners in the field of synaptic plasticity in motor control and behavior.
By studying sea slug's brain, we described that the strength of synaptic transmission is controled by its own activity level and by a neuromodulatory input. These two types of synaptic plasticity interact with each other to produce complex and dynamic changes in the strength of the synapse. Such changes may play important roles in configuration of neural circuit to produce specific motor outputs.
Although the development of techniques using brain slice preparations had made a great advance in our knowledge of synaptic plasticity, I am hoping that this paper shows that researches in invertebrate neuroscience are still front runners in the field of synaptic plasticity in motor control and behavior.
Tuesday, December 9, 2008
Homeostatic Control of Neural Function: From Phenomenology to Molecular Design
Grae Davis gave a Brains and Behavior talk entitled, "Homeostatic Control of Neural Function: From Phenomenology to Molecular Design".
He talked about homeostasis of the transmitter release that compensates reduced sensitivity or motoneuronal innervation of the postsynaptic muscle. If postsynaptic GluR was blocked by a toxin, the frequency of mEPSC increases and the size of EPSP recovers in 10 min. This was shown also by some mutants.
This recovery of EPSP amplitude is activity-independent. It seems like that the muscle is sensing the tonic release of transmitter from the presynaptic terminals, and release some retrograde messenger that regulates the transmitter release.
One candidate was called ephrins and Eph receptor.
He talked about homeostasis of the transmitter release that compensates reduced sensitivity or motoneuronal innervation of the postsynaptic muscle. If postsynaptic GluR was blocked by a toxin, the frequency of mEPSC increases and the size of EPSP recovers in 10 min. This was shown also by some mutants.
This recovery of EPSP amplitude is activity-independent. It seems like that the muscle is sensing the tonic release of transmitter from the presynaptic terminals, and release some retrograde messenger that regulates the transmitter release.
One candidate was called ephrins and Eph receptor.
Thursday, December 4, 2008
Thompson and Watson (2005) Melibe swim paper
Sint1 cell bodies are located on the medial dorsal surface just caudal to the prominent tentacular lobe that rises from the center of the pleural ganglion. 30-50 micron.
Sint1 branches in the pleural ganglion neuropil near the base of the optic lobe and projects to the ipsilateral pedal ganglion via the dorsal pleuralpedal connective, where it forms a series of arborizations.
A single sint2 is found near the dorsal midline of each pedal ganglion.
LY staining shows that sint2 branches in the pedal ganglion neuropil and sends a major process to the opposite pedal
ganglion via the circumesophageal, pedal-pedal connective.
sint1 can cause phase advance/delay.
There is reciprocal inhibition between left and right sint1 neurons, via direct IPSP.
sint1 innervates motoneurons.
sint1 and sint2 are electrically coupled.
Mutual inhibition between sint2 neurons.
Mutual inhibition between sint2 and the contralateral sint1
Activity in Sint1 and Sint2 dissociates during other locomotor behaviors.
the CPG for swimming is formed dynamically, when activity in the sint1 and sint2 cell pairs becomes bound together. When this does not occur, the same interneurons appear to function independently during the performance of other behaviors that involve the same or similar musculature, such as turning.
Sint1 branches in the pleural ganglion neuropil near the base of the optic lobe and projects to the ipsilateral pedal ganglion via the dorsal pleuralpedal connective, where it forms a series of arborizations.
A single sint2 is found near the dorsal midline of each pedal ganglion.
LY staining shows that sint2 branches in the pedal ganglion neuropil and sends a major process to the opposite pedal
ganglion via the circumesophageal, pedal-pedal connective.
sint1 can cause phase advance/delay.
There is reciprocal inhibition between left and right sint1 neurons, via direct IPSP.
sint1 innervates motoneurons.
sint1 and sint2 are electrically coupled.
Mutual inhibition between sint2 neurons.
Mutual inhibition between sint2 and the contralateral sint1
Activity in Sint1 and Sint2 dissociates during other locomotor behaviors.
the CPG for swimming is formed dynamically, when activity in the sint1 and sint2 cell pairs becomes bound together. When this does not occur, the same interneurons appear to function independently during the performance of other behaviors that involve the same or similar musculature, such as turning.
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