Golgi's method
Image:GolgiStainedPyramidalCell.jpg|thumb|A human neocortical pyramidal neuron stained via Golgi technique. Notice the apical dendrite extending vertically above the soma and the numerous basal dendrites radiating laterally from the base of the cell body. Photo by Bob Jacobs, Colorado College.
Image:Golgi Hippocampus.jpg|right|thumb|Drawing by Camillo Golgi of a hippocampus stained with the silver nitrate method
Image:Purkinje cell by Cajal.png|thumb|Drawing of a Purkinje cell in the cerebellum cortex done by Santiago Ramón y Cajal, clearly demonstrating the power of Golgi's staining method to reveal fine detail
Golgi's method is a silver staining technique that is used to visualize nervous tissue under light microscopy. The method was discovered by Camillo Golgi, an Italian physician and scientist, who published the first picture made with the technique in 1873. It was initially named the black reaction by Golgi, but it became better known as the Golgi stain or later, Golgi method. Golgi discovered this by introducing potassium and sodium into a chicken embryo.
Golgi staining was used by Spanish neuroanatomist Santiago Ramón y Cajal to discover a number of novel facts about the organization of the nervous system, inspiring the birth of the neuron doctrine. Ultimately, Ramón y Cajal improved the technique by using a method he termed "double impregnation". "Ramón y Cajal's "staining technique, still in use, is called Cajal's stain.
Mechanism
The cells in nervous tissue are densely packed, and little information on their structures and interconnections can be obtained if all the cells are stained. Furthermore, the thin filamentary extensions of neural cells, including the axon and the dendrites of neurons, are too slender and transparent to be seen with normal staining techniques. Golgi's method stains a limited number of cells at random in their entirety. The mechanism by which this happens is still largely unknown. Dendrites, as well as the cell soma, are clearly stained in brown and black and can be followed in their entire length, which allowed neuroanatomists to track connections between neurons and to make visible the complex networking structure of many parts of the brain and spinal cord.Golgi's staining is achieved by impregnating aldehyde-fixed nervous tissue with potassium dichromate and silver nitrate. Cells thus stained are filled by microcrystallization of silver chromate.
Technique
According to SynapseWeb, this is the recipe for Golgi's staining technique:- Immerse a block of formaldehyde-fixed brain tissue into a 2% aqueous solution of potassium dichromate for 2 days
- Dry the block shortly with filter paper.
- Immerse the block into a 2% aqueous solution of silver nitrate for another 2 days.
- Cut sections approx. 20–100 μm thick.
- Dehydrate quickly in ethanol, clear and mount.