Flyer

Journal of Neurology and Neuroscience

  • ISSN: 2171-6625
  • Journal h-index: 17
  • Journal CiteScore: 4.12
  • Journal Impact Factor: 3.20
  • 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

Mini Review - (2023) Volume 14, Issue 1

Blood-brain barrier: Challenges and opportunities for the treatment of neurological disorders

Liangfang Schwartz*
 
Department of Pharmacology, University of California, San Diego, USA
 
*Correspondence: Liangfang Schwartz, Department of Pharmacology, University of California, San Diego, USA, Email:

Received: 31-Dec-2022, Manuscript No. ipjnn-23-13635; Editor assigned: 03-Jan-2023, Pre QC No. P-13635; Reviewed: 17-Jan-2023, QC No. Q-13635; Revised: 23-Jan-2023, Manuscript No. R-13635; Published: 31-Jan-2023

Abstract

The blood-brain barrier (BBB) is a specialized system of blood vessels that controls the exchange of substances between the blood and the brain. It is composed of tightly packed endothelial cells, surrounded by astrocytes and pericytes, which create a selective barrier that restricts the passage of molecules based on their size, polarity, and charge. The BBB serves as a protective barrier, preventing the entry of harmful substances while allowing essential nutrients to pass through. However, it can also limit the delivery of therapeutic drugs to the brain, posing a challenge for the treatment of neurological disorders. The BBB is a complex and fascinating system that continues to be the subject of ongoing research in neuroscience and pharmacology.

Keywords

Blood-brain barrier; Endothelial cells; Astrocytes; Selective barrier; Protective barrier

Keywords

Blood-brain barrier; Endothelial cells; Astrocytes; Selective barrier; Protective barrier

Introduction

The blood-brain barrier (BBB) is a highly specialized system of blood vessels that regulates the exchange of substances between the circulating blood and the brain. It is a complex and intricate structure that plays a crucial role in maintaining the brain's homeostasis by preventing the entry of harmful substances, while allowing essential nutrients and gases to pass through. The BBB is composed of tightly packed endothelial cells that line the walls of brain capillaries, which are surrounded by astrocytes and pericytes. Together, these cells create a selective barrier that restricts the passage of molecules based on their size, polarity, and charge. While the BBB serves as an important protective barrier, it can also limit the delivery of therapeutic drugs to the brain, posing a challenge for the treatment of neurological disorders. In this context, understanding the function and regulation of the BBB is a critical area of research in the fields of neuroscience and pharmacology [1].

Literature Review

The blood-brain barrier (BBB) is a highly specialized system of blood vessels that protects the brain from harmful substances and regulates the exchange of essential nutrients and gases. The BBB is composed of tightly packed endothelial cells, surrounded by astrocytes and pericytes, which create a selective barrier that restricts the passage of molecules based on their size, polarity, and charge [2]. Understanding the function and regulation of the BBB is critical for the treatment of neurological disorders, as it can limit the delivery of therapeutic drugs to the brain. Recent studies have shed light on the molecular mechanisms underlying BBB transport and regulation. Transporters, such as P-glycoprotein (P-gp), play a critical role in controlling the entry of drugs into the brain. Various physiological and pathological factors, such as inflammation and hypoxia, can alter BBB permeability and disrupt its function [3].

In addition to its protective function, the BBB also plays a crucial role in maintaining the brain's homeostasis by regulating the exchange of essential nutrients and gases. For example, glucose transport across the BBB is mediated by specific transporters, such as GLUT1 and SGLT1, which are critical for brain metabolism. Furthermore, advances in imaging technologies, such as magnetic resonance imaging (MRI) and positron emission tomography (PET), have allowed for non-invasive visualization and quantification of BBB function in vivo. These techniques have enabled researchers to study BBB dysfunction in various neurological disorders, such as Alzheimer's disease and stroke. Overall, the BBB is a complex and fascinating system that continues to be the subject of ongoing research and investigation in the fields of neuroscience and pharmacology. Further understanding of the BBB's function and regulation could lead to the development of novel treatments for neurological disorders [4].

Discussion

The blood-brain barrier (BBB) is a critical component of the central nervous system that regulates the exchange of substances between the blood and the brain. The BBB serves as a protective barrier, preventing the entry of harmful substances into the brain while allowing essential nutrients to pass through. However, it can also limit the delivery of therapeutic drugs to the brain, posing a challenge for the treatment of neurological disorders. Recent research has shed light on the molecular mechanisms underlying BBB transport and regulation. Understanding these mechanisms is crucial for the development of novel treatments for neurological disorders. Transporters, such as P-glycoprotein (P-gp), play a critical role in controlling the entry of drugs into the brain. Targeting these transporters could enhance the delivery of therapeutic drugs to the brain, improving their efficacy [5].

Furthermore, advances in imaging technologies have enabled researchers to study BBB dysfunction in various neurological disorders. For example, studies have shown that BBB dysfunction plays a role in the pathogenesis of Alzheimer's disease and stroke. Understanding the role of BBB dysfunction in these diseases could lead to the development of new diagnostic tools and therapies. In addition, recent studies have highlighted the potential of the BBB as a target for drug development. By selectively targeting the BBB, drugs could be delivered specifically to the brain, minimizing off-target effects and improving therapeutic outcomes.However, challenges remain in developing effective therapies that can cross the BBB. The selective barrier properties of the BBB limit the entry of large molecules, such as therapeutic proteins, into the brain. Strategies such as nanoparticle-based drug delivery systems and the use of cell-penetrating peptides are being explored to overcome these challenges [6].

Conclusion

The BBB is a critical component of the central nervous system that regulates the exchange of substances between the blood and the brain. Advances in our understanding of BBB function and regulation have the potential to lead to the development of novel treatments for neurological disorders. However, challenges remain in developing effective therapies that can cross the BBB, and further research is needed to overcome these challenges.

Acknowledgement

None.

Conflict of Interest

None.

References

  1. Abbott NJ, Patabendige AA, Dolman DE, et al. Structure and function of the blood–brain barrier. Neurobiol Dis. 2010; 37(1):13-25.
  2. Google Scholar, Crossref, Indexed at

  3. Daneman R, Prat A. The blood–brain barrier. Cold Spring Harb Perspect Biol. 2015; 7(1):a020412.
  4. Google Scholar, Crossref, Indexed at

  5. Chen X, Ghribi O, Geiger JD. Caffeine protects against disruptions of the blood-brain barrier in animal models of Alzheimer's and Parkinson's diseases. Am J Alzheimer's Dis. 2010; 20(s1):127-141.
  6. Google Scholar, Crossref, Indexed at

  7. Lajoie JM, Shusta EV. Targeting receptor-mediated transport for delivery of biologics across the blood-brain barrier. Annu Rev Pharmacol Toxicol. 2015; 55:613-631.
  8. Google Scholar, Crossref, Indexed at

  9. Obermeier B, Daneman R, Ransohoff RM. Development, maintenance and disruption of the blood-brain barrier. Nat med. 2013; 19(12):1584-1596.
  10. Google Scholar, Crossref, Indexed at

  11. Pardridge WM. Blood–brain barrier drug delivery of IgG fusion proteins with a transferrin receptor monoclonal antibody. Expert Opin Drug Deliv. 2015; 12(2):207-222.
  12. Google Scholar, Crossref, Indexed at