Adult Brain Repair of Neural Damage

Azhar Noor^*
*Correspondence: Azhar Noor, Department of Neurorehabiliation, University of Greifswald Greifswald, Germany, Email:

Keywords

Brain damage • Chronic brain injury • Cell damage

Introduction

Acute or chronic brain damage in adults frequently results in significant loss of neuronal tissue and persistent functional disability. A number of treatments have been developed over the last two decades to harness the regenerative potential of neural stem cells and the current destiny flexibility of neural cells in the nervous system to avoid tissue loss or improve structural and functional regeneration following damage. We examine current obstacles and limitations in stem cell-associated neural healing in the adult brain, as well as potential approaches for advancing experimental stem cell therapies into the clinic [1,2].

Following extensive training and rehabilitation, a significant number of patients regain their ability to talk and communicate:

• Similarly, the brain can compensate effectively before the consequences of significant loss of neuronal tissue become apparent

• Before Parkinson's symptoms appear, more than 80% of dopaminergic neurons in the substantia nigra are thought to be damaged

• As a result, the adult mammalian brain's ability to repair itself—at least functionally—is obvious.

• These endogenous repair processes have obvious limitations, leaving a significant percentage of adult brain damage patients with lasting functional abnormalities. As a result, fresh ways for treating degenerative or traumatic brain illnesses must be devised. Exogenous cells have been used in the illness context to either recruit or augment endogenous healing processes or to improve brain function by supplying exogenous cells via transplantation.

• We concentrate solely on existing methodologies and concepts for enhancing brain healing using endogenous neural stem cells (NSCs) or other neural cells.

NSCs make new neurons in specific locations of the adult brain15, which can be used to target endogenous neurogenesis for brain repair [3-5].

Neurogenesis

One of these is the SVZ, which lines the lateral ventricles and is where NSCs give birth to newborn cells that migrate along the rostral migratory stream into the olfactory bulb (OB), where they differentiate into several types of olfactory neurons. In the rodent brain, SVZ/OB neurogenesis is relatively active, whereas in the human brain, the neurogenic activity of the SVZ appears to be very low or non-existent. In contrast, the hippocampus DG, where NSCs give rise to DG granule cells throughout life, is the second major neurogenic region.

Glial repair with neural stem cells

The destiny potential of endogenous NSCs also allows for targeting NSCs to assist glial cell replacement and eventual brain repair, in addition to techniques aimed at enhancing endogenous neurogenesis for neuronal repair in the context of acute or chronic illness. Demyelination in the mouse SVZ [6], for example, has been shown to result in increased NSC-derived oligodendrocyte production, which may aid in the remyelination of the wounded brain following a lesion76,77. Induced production of oligodendrocytes (which are not produced by DG NSCs under normal conditions) could be used to induce remyelination of the DG circuitry in a variety of demyelinating disorders, including multiple sclerosis and epilepsy78–81. However, possible therapeutic techniques aimed at using endogenous NSCs for glial repair are still being developed, and more research is needed. [7-9]

Acknowledgement

Not applicable.

Conflict of Interest

There is no conflict of interest by author.

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