Flyer

Journal of Neurology and Neuroscience

  • ISSN: 2171-6625
  • Journal h-index: 18
  • Journal CiteScore: 4.35
  • Journal Impact Factor: 3.75
  • Average acceptance to publication time (5-7 days)
  • Average article processing time (30-45 days) Less than 5 volumes 30 days
    8 - 9 volumes 40 days
    10 and more volumes 45 days
Awards Nomination 20+ Million Readerbase
Indexed In
  • Open J Gate
  • Genamics JournalSeek
  • The Global Impact Factor (GIF)
  • China National Knowledge Infrastructure (CNKI)
  • Directory of Research Journal Indexing (DRJI)
  • OCLC- WorldCat
  • Proquest Summons
  • Scientific Journal Impact Factor (SJIF)
  • Euro Pub
  • Google Scholar
  • Secret Search Engine Labs
Share This Page

Commentary - (2024) Volume 15, Issue 5

The regenerative brain mechanisms and implications of neurogenesis

Giorgia Marino*
 
Department of Neurosurgery, ASST Ovest Milano Legnano Hospital, 20025 Legnano, Milan, Italy
 
*Correspondence: Giorgia Marino, Department of Neurosurgery, ASST Ovest Milano Legnano Hospital, 20025 Legnano, Milan, Italy, Email:

Received: 03-Oct-2024, Manuscript No. ipjnn-24-15393; Editor assigned: 05-Oct-2024, Pre QC No. P-15393; Reviewed: 18-Oct-2024, QC No. Q-15393; Revised: 24-Oct-2024, Manuscript No. R-15393; Published: 31-Oct-2024

Introduction

Neurogenesis, the process through which new neurons are formed in the brain, has emerged as a fascinating field of study, challenging the long-held belief that the adult brain is incapable of generating new cells. Traditionally, it was thought that neurogenesis only occurred during development and ceased shortly after birth. However, groundbreaking research over the past few decades has demonstrated that neurogenesis can persist into adulthood, particularly in specific regions of the brain, such as the hippocampus, which is associated with memory and learning. This article explores the mechanisms underlying neurogenesis, its implications for brain health, and its potential applications in treating neurological disorders [1].

Neurogenesis involves a series of complex processes, including the proliferation of Neural Stem Cells (NSCs), their differentiation into mature neurons, and the integration of these neurons into existing neural circuits. Neural stem cells are undifferentiated cells with the ability to self-renew and differentiate into various types of brain cells, including neurons, astrocytes, and oligodendrocytes. In adult mammals, these stem cells are primarily located in the subgranular zone of the dentate gyrus, part of the hippocampus. Under certain conditions, such as physical exercise, environmental enrichment, and learning, these NSCs can be stimulated to divide and differentiate. Under favorable conditions, NSCs enter the cell cycle, proliferating to form a population of progenitor cells [2].

These progenitor cells can then differentiate into neuroblasts, which will ultimately mature into functional neurons. Newly formed neurons extend their axons and dendrites, forming synapses and integrating into existing neural networks. The process of neurogenesis is regulated by various intrinsic and extrinsic factors, including growth factors, neurotransmitters, and environmental stimuli. Brain-Derived Neurotrophic Factor (BDNF) is one of the most studied neurotrophic factors, playing a critical role in promoting the survival, growth, and differentiation of neurons. Neurogenesis is influenced by a multitude of factors, both positive and negative. Understanding these factors is crucial for harnessing neurogenesis in therapeutic contexts. Regular aerobic exercise has been shown to significantly enhance neurogenesis. Exercise increases levels of BDNF and promotes blood flow to the brain, which provides essential nutrients and oxygen [3].

Description

Exposure to a stimulating environment with opportunities for exploration and social interaction can enhance neurogenesis. This includes exposure to novel experiences and challenges that promote cognitive engagement. Engaging in tasks that require learning can also promote neurogenesis. The acquisition of new skills and knowledge stimulates the production of neurotrophic factors and creates a demand for new neurons. Certain dietary components, such as omega-3 fatty acids found in fish, and polyphenols present in fruits and vegetables, have been linked to enhanced neurogenesis. Prolonged exposure to stress hormones, particularly cortisol, can inhibit neurogenesis. Stress reduces the proliferation of NSCs and can lead to the atrophy of the hippocampus. While neurogenesis occurs throughout life, its efficiency declines with age. Aging is associated with reduced neurogenic activity, which may contribute to cognitive decline and increased susceptibility to neurodegenerative diseases [4].

Alcohol and drugs can negatively affect neurogenesis. Chronic alcohol consumption has been shown to reduce the proliferation of NSCs and impair the integration of new neurons. Chronic inflammation, often seen in various neurological disorders, can inhibit neurogenesis. Pro-inflammatory cytokines can impair the survival and function of newly formed neurons. The ability of the brain to generate new neurons has significant implications for brain health, cognitive function, and the treatment of neurological disorders. Neurogenesis in the hippocampus is closely linked to learning and memory. Studies have shown that increased neurogenesis can enhance cognitive function, improve memory retention, and facilitate the ability to adapt to new information. Conversely, a decline in neurogenesis has been associated with cognitive impairments and memory deficits, particularly in aging populations [5].

Emerging evidence suggests that neurogenesis plays a role in mood regulation and mental health. For instance, individuals suffering from depression often exhibit reduced neurogenic activity. Antidepressant treatments, particularly those that increase levels of BDNF, have been shown to promote neurogenesis, highlighting a potential mechanism through which these treatments exert their effects. Moreover, neurogenesis may be implicated in the brain's ability to recover from traumatic experiences. Enhancing neurogenesis could provide a therapeutic avenue for individuals suffering from Post-Traumatic Stress Disorder (PTSD) and other trauma-related conditions.

The potential for neurogenesis to contribute to recovery from neurodegenerative diseases, such as Alzheimer’s and Parkinson’s, is an area of intense research. While neurogenesis alone may not be sufficient to replace the vast loss of neurons in these diseases, enhancing neurogenic pathways could help to improve cognitive function and delay the progression of symptoms. Strategies that promote neurogenesis, including physical activity, cognitive training, and dietary modifications, are being investigated as adjunctive therapies to conventional treatments for neurodegenerative diseases. Given the central role of neurogenesis in brain health, researchers are exploring various therapeutic applications aimed at enhancing this process. Several pharmacological agents are being investigated for their potential to promote neurogenesis. For example, certain antidepressants, such as Selective Serotonin Reuptake Inhibitors (SSRIs), have been shown to increase the proliferation of NSCs.

Lifestyle modifications can play a crucial role in promoting neurogenesis. Encouraging physical activity, cognitive engagement, and a balanced diet rich in nutrients that support brain health may provide non-invasive strategies for enhancing neurogenic activity. Developing community-based exercise programs tailored for older adults can encourage regular physical activity and improve cognitive function through enhanced neurogenesis. Programs that promote cognitive engagement through puzzles, learning new skills, or social interactions can stimulate neurogenesis and improve mental health. Dietary recommendations that emphasize the consumption of omega-3 fatty acids, antioxidants, and other neuroprotective nutrients could help maintain neurogenic activity throughout life. Innovative therapeutic approaches, such as stem cell therapy, are being explored as potential treatments for neurological disorders. By transplanting NSCs or inducing endogenous NSCs to proliferate and differentiate, researchers aim to repair damaged neural circuits and restore function in the brain. While still in experimental stages, these approaches hold promise for conditions characterized by significant neuronal loss, such as stroke, traumatic brain injury, and neurodegenerative diseases.

Conclusion

The discovery of neurogenesis in the adult brain has profound implications for our understanding of brain health and disease. By elucidating the mechanisms that regulate neurogenesis, we open the door to potential therapeutic strategies that can enhance cognitive function, improve mental health, and mitigate the effects of neurodegenerative diseases. As research continues to uncover the intricate relationship between neurogenesis and various factors influencing brain health, it is imperative to integrate this knowledge into public health initiatives, clinical practice, and lifestyle interventions. The regenerative potential of the brain underscores the importance of nurturing our neurological health throughout our lives, paving the way for a future where the brain’s capacity for renewal is harnessed to improve quality of life and cognitive resilience. Understanding and promoting neurogenesis not only enriches our grasp of the brain’s capabilities but also illuminates new pathways for therapeutic intervention in an era where mental health and cognitive vitality are of paramount importance.

Acknowledgement

None.

Conflict of Interest

None.

References

  1. Allyn MM, Luo RH, Hellwarth EB, et al. Considerations for polymers used in ocular drug delivery. Front Med 2022; 8:787644.
  2. Google Scholar, Crossref, Indexed at

  3. Xing Y, Zhu L, Zhang K, et al. Nanodelivery of triamcinolone acetonide with plga-chitosan nanoparticles for the treatment of ocular inflammation. Artif cells nanomed biotechnol. 2021; 49(1):308-316.
  4. Google Scholar, Crossref, Indexed at

  5. Wu KY, Tan K, Akbar D, et al. A new era in ocular therapeutics: Advanced drug delivery systems for uveitis and neuro-ophthalmologic conditions. Pharmaceutics. 2023; 15(7):1952.
  6. Google Scholar, Crossref, Indexed at

  7. Tettamanti M, Buccino G, Saccuman MC, et al. Listening to action-related sentences activates fronto-parietal motor circuits. J Cogn Neurosci. 2005; 17(2):273-281.
  8. Google Scholar, Crossref, Indexed at

  9. Pulvermüller F, Hauk O, Nikulin VV, Ilmoniemi RJ. Functional links between motor and language systems. Eur J Neurosci. 2005; 21(3):793-797.
  10. Google Scholar, Crossref, Indexed at