Neurodegenerative diseases are a group of devastating disorders that result in a gradual decline of cognitive function, movement control, and various other important neurological processes. Millions of people across the world suffer from these diseases, placing a significant burden on healthcare systems, caregivers, and economies. As populations and life expectancies increase, the prevalence of these conditions continues to rise.
Alzheimer’s disease (AD), Parkinson’s disease (PD), multiple sclerosis (MS), and amyotrophic lateral sclerosis (ALS) are among the most common of the diseases that fall under this umbrella and, despite their difference in disease etiology and treatment, the degenerative nature and some downstream effects of each disease are relatively similar. (2)
While understanding the specific genetic and/or biological mechanisms that cause each disease is essential, understanding the common consequences (such as tissue damage and immune response) and how they contribute to disease progression can be equally important. This article is meant to discuss one of the consequences that neurodegenerative diseases share: dysfunction of the blood-brain barrier (BBB).
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What is the BBB?
The BBB is a physical weapon designed by your body specifically to protect your most important and irreplaceable organ – your brain! Just as a guard monitors and filters people entering a restricted area, the BBB is highly selective about which molecules, ions, and cells are allowed to enter the brain from the bloodstream.
While most organs in the body have barriers to protect against potentially harmful things in the bloodstream, the barrier in the brain is superior. The BBB consists of 3 different cell types (endothelial cells, pericytes, and astrocytes) along with membranes (a matrix), which work as a team to line the blood vessels in the brain and create the most selective barrier in your body. (3, 4)
What is its purpose?
The BBB is working to protect your brain 24/7, but it is especially important in times of illness. For example, viruses and bacteria can circulate in the bloodstream. Without the BBB, these pathogens can enter the brain and wreak havoc on the brain’s well-maintained homeostasis, causing encephalitis (inflammation of the brain), meningitis (inflammation of the membranes surrounding the brain and spinal cord), or interrupting other neurological systems.
This selective permeability of the BBB is vital in maintaining the overall health and function of the central nervous system (CNS).
BBB Damage
Similar to a security breach, which compromises the safety of a protected area, damage to the BBB allows for increased permeability into the brain, leaving the brain vulnerable to harmful substances circulating in the bloodstream. The BBB can become damaged for various reasons. In neurodegenerative diseases, though, the most common reasons include:
Inflammation:
Immune cells in the brain produce various signals called cytokines and chemokines in response to the disease pathology. These signals trigger inflammation and can induce changes in the cells that make up the BBB. (6)
Oxidative Stress:
This type of stress occurs when there is an imbalance in reactive oxygen species (ROS) and the body’s ability to detoxify them. (7)
ROS are highly reactive molecules that directly damage important cellular components, including cell membranes, proteins, and DNA.
Disease Pathology:
The specific mechanisms of each neurological disease can play a large role in the dysfunction of the BBB. Amyloid-β (Aβ), one of the major proteins involved in AD, can directly interact with and damage the endothelial cells that make up the BBB.
Aging:
As with neurodegenerative diseases, BBB damage can also occur naturally with aging in the absence of underlying conditions. (9)
Consequences of BBB Damage
Once the BBB is damaged, the following consequences only exacerbate the disease pathology. What was once a protective barrier can then allow harmful agents to infiltrate the brain, leading to various downstream effects.
Immune Cell Infiltration
Chronic neuroinflammation is a major consequence of BBB damage. The brain is often referred to as an “immune privileged” site. This means that the brain has its own immune cells, which are separate from the peripheral body, enabling the brain to have high control over immunity and inflammation. (10)
When the BBB is compromised, immune cells from the body can infiltrate the brain in response to the various signals produced from the disease (i.e., signals released from cell death or damage), where they contribute to inflammation and cause further damage. (11)
Toxin Accumulation
With increased permeability, toxic substances that are normally kept out of the brain can accumulate. These toxins can include heavy metals, environmental pollutants, and metabolic waste products. Their presence can contribute to neuronal injury and cell death. (9)
Impaired Nutrient Delivery
The BBB plays a crucial role in regulating the transport of essential nutrients, such as glucose, amino acids, vitamins, and minerals, from the bloodstream into the brain.
When the BBB is compromised, either due to dysfunction or damage, the delivery of nutrients to the brain can be impaired in several ways at the endothelial cell receptor and transporter level, the major players in biomolecules and nutrient transportation. (12)
Neuronal Damage
While neurodegenerative diseases cause neuronal damage and cell death through their own pathology, damage to the BBB elevates this. As a result of the above consequences, inflammation and toxin accumulation directly impact neuronal cell health.
How to Protect Your BBB
Because BBB dysfunction can happen naturally with age, maintaining a healthy lifestyle is the best course of action to strengthen your BBB. Eating healthy meals, exercising regularly, managing stress, achieving adequate amounts of sleep, and limiting drug and alcohol consumption can all help to protect your BBB from damage. (13, 14)
Eating foods that are rich in omega-3 fatty acids can also aid in BBB protection. Studies have shown significant correlations between omega-3-fatty acid foods and BBB integrity likely attributed to their potent anti-inflammatory effects and support of vascular health by maintaining endothelial cell function, the cells that line the BBB.
Identifying BBB Damage
While BBB dysfunction is presumed and treated in neurodegenerative disorders, there are ways to test BBB permeability. These technologies are particularly useful for disease monitoring.
Advanced Imaging Studies
Advanced brain imaging techniques, such as magnetic resonance imaging (MRI) can detect structural changes in the brain associated with BBB damage. (16)
When used in combination with dyes that are injected into the bloodstream, commonly called dynamic contrast-enhanced MRI (DCE-MRI), BBB permeability can be visualized and measured. When these dyes cannot pass a healthy BBB, leakage of these dyes into the brain indicates BBB damage.
A similar technique with computer tomography (CT) has also been shown to be successful. These techniques can be challenging, though, since BBB leakage tends to be subtle despite its disastrous effects.
Lab Testing
Examination of cerebrospinal fluid (CSF) can provide insights into BBB function and integrity. Elevated levels of proteins, such as albumin or immunoglobulins, in the CSF compared to blood can indicate BBB dysfunction. (19)
Albumin concentration is typically high in the blood and low in CSF; however, during BBB damage, albumin can enter the brain during BBB damage, increasing the concentration of albumin in the CSF. (20)
Similarly, immunoglobulins, which are typically found in the blood, can have various effects once crossing into the CNS. (21)
Blood biomarkers can also indicate BBB disruption or neuroinflammation. For example, elevated levels of matrix metalloproteinases (MMPs) or cytokines in the blood may suggest BBB damage. (22, 23)
In some cases, a brain biopsy may be performed to directly assess BBB integrity and identify pathological changes associated with BBB dysfunction. This method is invasive and is typically reserved for cases where other diagnostic methods are inconclusive.
Treatment and Challenges
Treating BBB damage will depend on the underlying causes (e.g. disease etiology), reducing inflammation, and promoting repair of the barrier. This can be achieved through therapeutic intervention as well as lifestyle modifications.
Anti-Inflammatory Therapy
Because inflammation plays a major role in BBB damage, the use of anti-inflammatory drugs is often a first line of defense when choosing a treatment route. Targeting the neuroinflammatory aspect of BBB damage can promote tissue repair and help restore the barrier. Non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and immunosuppressive drugs are the most common. (25)
Neuroprotective Agents
Certain medications or supplements with neuroprotective properties may help to support BBB repair and prevent further damage. This includes omega-3 fatty acids and polyphenols. (26)
Blood Pressure Management
High blood pressure can contribute to BBB damage through vascular stress and promoting inflammation. Monitoring and treating blood pressure accordingly can help to slow or prevent further damage. (27)
Managing Underlying Conditions
Treating the neurological disorder itself helps to alleviate BBB dysfunction by targeting the damage at its source. Medical interventions vary for each disease.
Ongoing Research
Because of the impact that BBB damage has on brain inflammation and neurodegeneration, research is underway to develop therapies that can promote BBB repair. Emerging studies have demonstrated success in therapeutics that target frizzled (FZD) receptors and the Wnt pathway. (29)
While repairing the BBB may not cure neurodegenerative diseases, it may be possible to help slow disease progression and improve side effects.
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Key Takeaways
Overall, BBB dysfunction is increasingly recognized as a significant factor in the pathogenesis of neurodegenerative diseases.
Understanding the mechanisms underlying BBB dysfunction and developing strategies to preserve or restore BBB integrity may hold promise for the prevention and treatment of these devastating conditions.
Neurodegenerative diseases are a group of challenging disorders that may lead to a gradual decline in cognitive function, movement control, and various other important neurological processes. Many people across the world experience these diseases, which can place a significant burden on healthcare systems, caregivers, and economies. As populations and life expectancies increase, the prevalence of these conditions continues to rise.
Alzheimer’s disease (AD), Parkinson’s disease (PD), multiple sclerosis (MS), and amyotrophic lateral sclerosis (ALS) are among the most common of the diseases that fall under this umbrella. Despite their differences in disease origins and management, the degenerative nature and some downstream effects of each disease are relatively similar. (2)
While understanding the specific genetic and/or biological mechanisms that may contribute to each disease is essential, understanding the common consequences (such as tissue damage and immune response) and how they may contribute to disease progression can be equally important. This article is meant to discuss one of the consequences that neurodegenerative diseases may share: dysfunction of the blood-brain barrier (BBB).
[signup]
What is the BBB?
The BBB is a protective feature designed by your body specifically to safeguard your most important and irreplaceable organ – your brain! Just as a guard monitors and filters people entering a restricted area, the BBB is highly selective about which molecules, ions, and cells are allowed to enter the brain from the bloodstream.
While most organs in the body have barriers to protect against potentially harmful things in the bloodstream, the barrier in the brain is particularly selective. The BBB consists of 3 different cell types (endothelial cells, pericytes, and astrocytes) along with membranes (a matrix), which work as a team to line the blood vessels in the brain and create a highly selective barrier in your body. (3, 4)
What is its purpose?
The BBB works to protect your brain continuously, but it is especially important in times of illness. For example, viruses and bacteria can circulate in the bloodstream. Without the BBB, these pathogens could enter the brain and disrupt the brain’s well-maintained balance, potentially leading to conditions like encephalitis (inflammation of the brain), meningitis (inflammation of the membranes surrounding the brain and spinal cord), or affecting other neurological systems.
This selective permeability of the BBB is vital in maintaining the overall health and function of the central nervous system (CNS).
BBB Damage
Similar to a security breach, which compromises the safety of a protected area, damage to the BBB may allow for increased permeability into the brain, leaving the brain vulnerable to potentially harmful substances circulating in the bloodstream. The BBB can become damaged for various reasons. In neurodegenerative diseases, though, the most common reasons may include:
Inflammation:
Immune cells in the brain produce various signals called cytokines and chemokines in response to the disease pathology. These signals may trigger inflammation and induce changes in the cells that make up the BBB. (6)
Oxidative Stress:
This type of stress occurs when there is an imbalance in reactive oxygen species (ROS) and the body’s ability to manage them. (7)
ROS are highly reactive molecules that may directly affect important cellular components, including cell membranes, proteins, and DNA.
Disease Pathology:
The specific mechanisms of each neurological disease can play a large role in the dysfunction of the BBB. Amyloid-β (Aβ), one of the major proteins involved in AD, may directly interact with and affect the endothelial cells that make up the BBB.
Aging:
As with neurodegenerative diseases, BBB changes can also occur naturally with aging in the absence of underlying conditions. (9)
Consequences of BBB Damage
Once the BBB is affected, the following consequences may exacerbate the disease pathology. What was once a protective barrier can then allow potentially harmful agents to infiltrate the brain, leading to various downstream effects.
Immune Cell Infiltration
Chronic neuroinflammation is a major consequence of BBB damage. The brain is often referred to as an “immune privileged” site. This means that the brain has its own immune cells, which are separate from the peripheral body, enabling the brain to have high control over immunity and inflammation. (10)
When the BBB is compromised, immune cells from the body can infiltrate the brain in response to the various signals produced from the disease (i.e., signals released from cell death or damage), where they may contribute to inflammation and cause further changes. (11)
Toxin Accumulation
With increased permeability, substances that are normally kept out of the brain can accumulate. These substances can include heavy metals, environmental pollutants, and metabolic waste products. Their presence may contribute to neuronal injury and cell changes. (9)
Impaired Nutrient Delivery
The BBB plays a crucial role in regulating the transport of essential nutrients, such as glucose, amino acids, vitamins, and minerals, from the bloodstream into the brain.
When the BBB is compromised, either due to dysfunction or damage, the delivery of nutrients to the brain can be impaired in several ways at the endothelial cell receptor and transporter level, the major players in biomolecules and nutrient transportation. (12)
Neuronal Damage
While neurodegenerative diseases may cause neuronal changes and cell death through their own pathology, damage to the BBB can elevate this. As a result of the above consequences, inflammation and toxin accumulation may directly impact neuronal cell health.
How to Protect Your BBB
Because BBB dysfunction can happen naturally with age, maintaining a healthy lifestyle is a potential way to support your BBB. Eating balanced meals, exercising regularly, managing stress, achieving adequate amounts of sleep, and limiting drug and alcohol consumption may all help to support your BBB. (13, 14)
Including foods that are rich in omega-3 fatty acids may also aid in BBB support. Studies have shown significant correlations between omega-3-fatty acid foods and BBB integrity, likely attributed to their potential anti-inflammatory effects and support of vascular health by maintaining endothelial cell function, the cells that line the BBB.
Identifying BBB Damage
While BBB dysfunction is presumed and managed in neurodegenerative disorders, there are ways to test BBB permeability. These technologies are particularly useful for disease monitoring.
Advanced Imaging Studies
Advanced brain imaging techniques, such as magnetic resonance imaging (MRI), can detect structural changes in the brain associated with BBB damage. (16)
When used in combination with dyes that are injected into the bloodstream, commonly called dynamic contrast-enhanced MRI (DCE-MRI), BBB permeability can be visualized and measured. When these dyes cannot pass a healthy BBB, leakage of these dyes into the brain may indicate BBB changes.
A similar technique with computer tomography (CT) has also been shown to be successful. These techniques can be challenging, though, since BBB leakage tends to be subtle despite its potential effects.
Lab Testing
Examination of cerebrospinal fluid (CSF) can provide insights into BBB function and integrity. Elevated levels of proteins, such as albumin or immunoglobulins, in the CSF compared to blood can indicate BBB dysfunction. (19)
Albumin concentration is typically high in the blood and low in CSF; however, during BBB changes, albumin can enter the brain, increasing the concentration of albumin in the CSF. (20)
Similarly, immunoglobulins, which are typically found in the blood, can have various effects once crossing into the CNS. (21)
Blood biomarkers can also indicate BBB disruption or neuroinflammation. For example, elevated levels of matrix metalloproteinases (MMPs) or cytokines in the blood may suggest BBB changes. (22, 23)
In some cases, a brain biopsy may be performed to directly assess BBB integrity and identify pathological changes associated with BBB dysfunction. This method is invasive and is typically reserved for cases where other diagnostic methods are inconclusive.
Treatment and Challenges
Addressing BBB changes will depend on the underlying causes (e.g., disease origins), reducing inflammation, and promoting repair of the barrier. This can be achieved through therapeutic intervention as well as lifestyle modifications.
Anti-Inflammatory Therapy
Because inflammation plays a major role in BBB changes, the use of anti-inflammatory drugs is often a first line of defense when choosing a management route. Targeting the neuroinflammatory aspect of BBB changes can promote tissue repair and help support the barrier. Non-steroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and immunosuppressive drugs are the most common. (25)
Neuroprotective Agents
Certain medications or supplements with neuroprotective properties may help to support BBB repair and prevent further changes. This includes omega-3 fatty acids and polyphenols. (26)
Blood Pressure Management
High blood pressure can contribute to BBB changes through vascular stress and promoting inflammation. Monitoring and managing blood pressure accordingly may help to slow or prevent further changes. (27)
Managing Underlying Conditions
Addressing the neurological disorder itself may help to alleviate BBB dysfunction by targeting the changes at their source. Medical interventions vary for each disease.
Ongoing Research
Because of the impact that BBB changes have on brain inflammation and neurodegeneration, research is underway to develop therapies that can promote BBB repair. Emerging studies have demonstrated success in therapeutics that target frizzled (FZD) receptors and the Wnt pathway. (29)
While supporting the BBB may not address neurodegenerative diseases entirely, it may be possible to help slow disease progression and improve side effects.
[signup]
Key Takeaways
Overall, BBB dysfunction is increasingly recognized as a significant factor in the pathogenesis of neurodegenerative diseases.
Understanding the mechanisms underlying BBB dysfunction and developing strategies to preserve or restore BBB integrity may hold promise for the prevention and management of these challenging conditions.
1. Dugger BN, Dickson DW. Pathology of Neurodegenerative Diseases. Cold Spring Harb Perspect Biol. Jul 5 2017;9(7)doi:10.1101/cshperspect.a028035
2. Sweeney MD, Sagare AP, Zlokovic BV. Blood-brain barrier breakdown in Alzheimer disease and other neurodegenerative disorders. Nat Rev Neurol. Mar 2018;14(3):133-150. doi:10.1038/nrneurol.2017.188
3. Sweeney MD, Zhao Z, Montagne A, Nelson AR, Zlokovic BV. Blood-Brain Barrier: From Physiology to Disease and Back. Physiol Rev. Jan 1 2019;99(1):21-78. doi:10.1152/physrev.00050.2017
4. Kadry H, Noorani B, Cucullo L. A blood-brain barrier overview on structure, function, impairment, and biomarkers of integrity. Fluids Barriers CNS. Nov 18 2020;17(1):69. doi:10.1186/s12987-020-00230-3
5. Zhao N, Chung TD, Guo Z, et al. The influence of physiological and pathological perturbations on blood-brain barrier function. Front Neurosci. 2023;17:1289894. doi:10.3389/fnins.2023.1289894
6. Stephenson J, Nutma E, van der Valk P, Amor S. Inflammation in CNS neurodegenerative diseases. Immunology. Jun 2018;154(2):204-219. doi:10.1111/imm.12922
7. Enciu AM, Gherghiceanu M, Popescu BO. Triggers and effectors of oxidative stress at blood-brain barrier level: relevance for brain ageing and neurodegeneration. Oxid Med Cell Longev. 2013;2013:297512. doi:10.1155/2013/297512
8. Wan W, Cao L, Liu L, et al. Abeta(1-42) oligomer-induced leakage in an in vitro blood-brain barrier model is associated with up-regulation of RAGE and metalloproteinases, and down-regulation of tight junction scaffold proteins. J Neurochem. Jul 2015;134(2):382-93. doi:10.1111/jnc.13122
9. Knox EG, Aburto MR, Clarke G, Cryan JF, O'Driscoll CM. The blood-brain barrier in aging and neurodegeneration. Mol Psychiatry. Jun 2022;27(6):2659-2673. doi:10.1038/s41380-022-01511-z
10. Proulx ST, Engelhardt B. Central nervous system zoning: How brain barriers establish subdivisions for CNS immune privilege and immune surveillance. J Intern Med. Jul 2022;292(1):47-67. doi:10.1111/joim.13469
11. Berriat F, Lobsiger CS, Boillee S. The contribution of the peripheral immune system to neurodegeneration. Nat Neurosci. Jun 2023;26(6):942-954. doi:10.1038/s41593-023-01323-6
12. Campos-Bedolla P, Walter FR, Veszelka S, Deli MA. Role of the blood-brain barrier in the nutrition of the central nervous system. Arch Med Res. Nov 2014;45(8):610-38. doi:10.1016/j.arcmed.2014.11.018
13. Santiago JA, Potashkin JA. Physical activity and lifestyle modifications in the treatment of neurodegenerative diseases. Front Aging Neurosci. 2023;15:1185671. doi:10.3389/fnagi.2023.1185671
14. Kip E, Parr-Brownlie LC. Healthy lifestyles and wellbeing reduce neuroinflammation and prevent neurodegenerative and psychiatric disorders. Front Neurosci. 2023;17:1092537. doi:10.3389/fnins.2023.1092537
15. Barnes S, Chowdhury S, Gatto NM, Fraser GE, Lee GJ. Omega-3 fatty acids are associated with blood-brain barrier integrity in a healthy aging population. Brain Behav. Aug 2021;11(8):e2273. doi:10.1002/brb3.2273
16. Varatharaj A, Liljeroth M, Darekar A, Larsson HBW, Galea I, Cramer SP. Blood-brain barrier permeability measured using dynamic contrast-enhanced magnetic resonance imaging: a validation study. J Physiol. Feb 2019;597(3):699-709. doi:10.1113/JP276887
17. Sage MR, Wilson AJ, Scroop R. Contrast media and the brain. The basis of computed tomography and magnetic resonance imaging enhancement: A review. Australasian Radiology. 2001;44(2):133-142. doi:10.1046/j.1440-1673.2000.00797.x
18. Avsenik J, Bisdas S, Popovic KS. Blood-brain barrier permeability imaging using perfusion computed tomography. Radiol Oncol. Jun 2015;49(2):107-14. doi:10.2478/raon-2014-0029
19. Akaishi T, Narikawa K, Suzuki Y, et al. Importance of the quotient of albumin, quotient of immunoglobulin G and Reibergram in inflammatory neurological disorders with disease‐specific patterns of blood–brain barrier permeability. Neurology and Clinical Neuroscience. 2015;3(3):94-100. doi:10.1111/ncn3.158
20. Shojai S, Haeri Rohani SA, Moosavi-Movahedi AA, Habibi-Rezaei M. Human serum albumin in neurodegeneration. Rev Neurosci. Oct 26 2022;33(7):803-817. doi:10.1515/revneuro-2021-0165
21. Sim KY, Im KC, Park SG. The Functional Roles and Applications of Immunoglobulins in Neurodegenerative Disease. Int J Mol Sci. Jul 26 2020;21(15) doi:10.3390/ijms21155295
22. Janigro D, Bailey DM, Lehmann S, et al. Peripheral Blood and Salivary Biomarkers of Blood-Brain Barrier Permeability and Neuronal Damage: Clinical and Applied Concepts. Front Neurol. 2020;11:577312. doi:10.3389/fneur.2020.577312
23. Barr TL, Latour LL, Lee KY, et al. Blood-brain barrier disruption in humans is independently associated with increased matrix metalloproteinase-9. Stroke. Mar 2010;41(3):e123-8. doi:10.1161/STROKEAHA.109.570515
24. Claudio L. Ultrastructural features of the blood-brain barrier in biopsy tissue from Alzheimer’s disease patients. Acta Neuropathol. 1996;91:6-14.
25. Benito-Leon J, Contador I, Vega S, Villarejo-Galende A, Bermejo-Pareja F. Non-steroidal anti-inflammatory drugs use in older adults decreases risk of Alzheimer's disease mortality. PLoS One. 2019;14(9):e0222505. doi:10.1371/journal.pone.0222505
26. Yan L, Guo MS, Zhang Y, et al. Dietary Plant Polyphenols as the Potential Drugs in Neurodegenerative Diseases: Current Evidence, Advances, and Opportunities. Oxid Med Cell Longev. 2022;2022:5288698. doi:10.1155/2022/5288698
27. Katsi V, Marketou M, Maragkoudakis S, et al. Blood-brain barrier dysfunction: the undervalued frontier of hypertension. J Hum Hypertens. Oct 2020;34(10):682-691. doi:10.1038/s41371-020-0352-2
28. Martin M, Vermeiren S, Bostaille N, et al. Engineered Wnt ligands enable blood-brain barrier repair in neurological disorders. Science. Feb 18 2022;375(6582):eabm4459. doi:10.1126/science.abm4459
29. Wang Q, Huang X, Su Y, et al. Activation of Wnt/beta-catenin pathway mitigates blood-brain barrier dysfunction in Alzheimer's disease. Brain. Dec 19 2022;145(12):4474-4488. doi:10.1093/brain/awac236
30. Bats ML, Peghaire C, Delobel V, Dufourcq P, Couffinhal T, Duplaa C. Wnt/frizzled Signaling in Endothelium: A Major Player in Blood-Retinal- and Blood-Brain-Barrier Integrity. Cold Spring Harb Perspect Med. May 17 2022;12(4)doi:10.1101/cshperspect.a041219