Nissl stain

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Nissl Stain

The Nissl stain is a popular neurohistological staining method that was named after its developer, German psychiatrist and neuropathologist Franz Nissl. The stain is used primarily in the study of neurons and glial cells, the two main types of cells found in the nervous system.

History[edit | edit source]

The Nissl stain was developed in the late 19th century by Franz Nissl, who was seeking a method to visualize the internal structure of neurons. Nissl discovered that certain dyes, particularly thionin and cresyl violet, could selectively stain components within the neuron, allowing for detailed study of its structure.

Method[edit | edit source]

The Nissl stain works by binding to RNA, which is abundant in neurons. The stain is applied to a thin section of tissue, which is then examined under a microscope. The stained RNA appears dark blue or purple, allowing the observer to distinguish neurons and their components.

Applications[edit | edit source]

The Nissl stain is used in a variety of neurohistological studies. It is particularly useful in identifying changes in neuronal structure and function that occur in response to injury or disease. The stain can also be used to study the distribution and density of neurons in different regions of the brain.

Limitations[edit | edit source]

While the Nissl stain is a powerful tool for studying neurons, it has some limitations. It does not stain all components of the neuron equally, making it difficult to study certain structures. Additionally, the stain does not differentiate between different types of RNA, which can limit its usefulness in certain types of research.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD