In an electrical synapse communication is possible in both directions as ions and signals flow through the gap junctions
Electrical synapses allow for extremely fast, almost instantaneous transmission of charge, and so are able to be very interconnected and move all at once once specific signals are given
Electrical synapses are common in animals where instantaneous reflexes are needed for survival
presynaptic cells give signals to the postsynaptic cells
20 nm - 40 nm
length of a chemical synapse
Some chemical signals are excitatory and cause depolarization, others are inhibitory and cause hyperpolarization
Small vesicles
40 nm diameter, 30 micron volume, capable of transporting most of the smaller neurotransmitters we think about, tens of thousands at a time
Large dense-core vesicles
Diameters of 100 - 250 nm, transports peptides that are much larger than the other neurotransmitters
Vesicle
Tiny spheres of membrane lipids made for transporting things
Vesicular transports work because they use the outgoing H+ ions from their highly acidic inside environment to drag in the necessary neurotransmitters
Voltage-gated calcium channels
Large protein complexes that usually remain closed but open up and let Ca2+ flood in with its electrochemical gradient as soon as depolarization occurs
Full fusion
Vesicular membrane becomes fully exocytosed into the membrane and releases its contents
Kiss-and-run fusion
Incomplete fusion of the vesicle and the cell membrane where only some of the neurotransmitters are let free due to diffusion, then the vesicle detaches itself
Receptors
Proteins capable of sending a signal to change the function or activity of a neuron
Ionotropic receptors can be very selective because the amino acid residues on their active sites can repel certain ions (e.g. negative residue repels negative ions)
G proteins can break down GTP into GDP through catalysis, which powers the metabotropic receptor to open
Usually the alpha g-protein subunit becomes soluble while the beta and gamma subunits remain bound to the membrane
Dopamine receptor classes:
D1 and D5 are excitatory
D2 through D4 are inhibitory
Dopamine is also needed for motor control. When dopamine producing regions in the substantia nigra pars compacta (SNpc) are damaged, Parkinson's disease results, and it currently treated with exogenous dopamine
L-DOPA induced dyskinesia (LID)
Hyperkinesias caused by L-DOPA treatment of Parkinson's disease
Deep brain stimulation
Implanting a device that stimulates the brain to give back motor control to Parkinson's patients