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Unraveling the Source: Where does Cerebrolysin come from?

4 min read

Every year, millions suffer from neurological damage due to stroke, dementia, or brain injuries. In the search for effective treatments, one question often arises: Where does Cerebrolysin come from? This compound is derived from purified porcine (pig) brain proteins through a highly controlled process.

Quick Summary

Cerebrolysin is a pharmaceutical preparation made of low-molecular-weight neuropeptides and free amino acids. It originates from purified pig brains through a standardized enzymatic breakdown process.

Key Points

  • Origin: Cerebrolysin is a biological product derived from purified porcine (pig) brains through a patented enzymatic process.

  • Composition: It consists of a mixture of low-molecular-weight neuropeptides and free amino acids that can cross the blood-brain barrier.

  • Mechanism: It works in multiple ways, offering neuroprotection, promoting neurogenesis, and enhancing neuroplasticity.

  • Clinical Use: It is primarily used to treat ischemic stroke, traumatic brain injury, and various forms of dementia.

  • Regulatory Status: Cerebrolysin is approved in over 45 countries in Europe and Asia but is notably not approved by the US FDA.

  • Administration: It is administered via intramuscular injection or intravenous infusion, not orally.

In This Article

The Biological Origins of a Neurotrophic Agent

Cerebrolysin is a well-known peptide-based drug used in dozens of countries to treat a range of neurological and neurodegenerative disorders, including ischemic stroke, traumatic brain injury (TBI), and dementia. The fundamental question for many potential users and medical professionals is: Where does Cerebrolysin come from?

The answer lies in a sophisticated biotechnological process. Cerebrolysin is not a synthetic chemical but a biological preparation derived from porcine (pig) brains. The Austrian pharmaceutical company, EVER Neuro Pharma, developed and patented a method to create this compound. The process involves taking carefully selected and controlled raw brain material and subjecting it to a standardized enzymatic digestion. This procedure breaks down the high-molecular-weight proteins into smaller, biologically active low-molecular-weight peptides and free amino acids. The resulting solution is then rigorously purified and filtered to ensure its safety and consistency, removing any unwanted larger proteins, prions, viruses, or other contaminants. The final product is a sterile, ready-to-inject solution containing peptides with molecular weights of less than 10 kilodaltons (kDa).

Composition: What's Inside Cerebrolysin?

Cerebrolysin's therapeutic effects are attributed to its unique composition, which mimics the action of natural neurotrophic factors found in the human body. Although it's a complex mixture, its main active components are:

  • Low-Molecular-Weight Neuropeptides: These make up approximately 25% of the compound. These short chains of amino acids are small enough to cross the blood-brain barrier, allowing them to exert their effects directly within the central nervous system. They are believed to be the primary drivers of Cerebrolysin's neuro-restorative properties.
  • Free Amino Acids: Comprising the other 75%, these amino acids serve as essential building blocks for protein synthesis and neurotransmitter production within the brain. They support the overall metabolic health of neuronal cells.

Research has shown that Cerebrolysin contains peptides that have similar effects to endogenous neurotrophic factors like Brain-Derived Neurotrophic Factor (BDNF), Glial Cell Line-Derived Neurotrophic Factor (GDNF), and Ciliary Neurotrophic Factor (CNTF). These factors are crucial for the survival, differentiation, and growth of neurons.

Mechanism of Action: How Does It Work?

Cerebrolysin's efficacy stems from its multimodal mechanism of action, which addresses several key aspects of neuronal damage and repair. It is often described as having pleiotropic effects, meaning it produces multiple effects from a single compound.

  1. Neurotrophic Regulation: It promotes neurogenesis (the creation of new neurons) and enhances the survival of existing ones. By mimicking natural growth factors, it supports the brain's innate ability to repair itself.
  2. Neuroprotection: It protects neurons from damaging processes. This includes shielding them from excitotoxicity (damage caused by overstimulation from neurotransmitters like glutamate), preventing apoptosis (programmed cell death), and reducing inflammation and oxidative stress that typically follow a brain injury.
  3. Neuroplasticity: It improves synaptic function and plasticity. This involves modulating the formation and strengthening of connections between neurons, which is the cellular basis for learning, memory, and functional recovery after an injury.

This combination of effects allows Cerebrolysin to not only protect the brain during acute injury but also to support long-term recovery and cognitive function.

Clinical Applications and Regulatory Status

Cerebrolysin is approved for clinical use in over 45 countries, primarily in Europe and Asia. Its main indications are:

  • Acute Ischemic Stroke: Used to limit brain damage and improve functional outcomes.
  • Traumatic Brain Injury (TBI): Administered to reduce secondary injury and support cognitive recovery.
  • Dementia: Prescribed for vascular dementia and Alzheimer's disease to slow cognitive decline and improve daily functioning.

It is crucial to note that Cerebrolysin is not approved by the U.S. Food and Drug Administration (FDA). In the United States, it cannot be marketed or sold as a medical treatment. However, it can often be purchased for personal use as a 'dietary supplement' or 'research compound', but its legal status can be complex. Patients considering its use in regions where it is not approved should proceed with caution and consult with a qualified healthcare professional.

Comparison of Neurotrophic Agents

To better understand Cerebrolysin, it's helpful to compare it to similar compounds.

Feature Cerebrolysin Cortexin Conventional Nootropics (e.g., Piracetam)
Origin Porcine (pig) brain Bovine (cattle) & porcine (pig) cerebral cortex Synthetic (lab-created)
Composition Peptides (<10 kDa) & free amino acids Polypeptides (<10 kDa) Single chemical compound
Mechanism Multimodal: Neurotrophic, Neuroprotective Multimodal: Neurotrophic, Neuroprotective Primarily modulates neurotransmitter systems
Administration Intramuscular or Intravenous injection/infusion Intramuscular injection Oral (pills or powder)
Regulatory Status Approved in many EU/Asian countries; Not FDA approved Approved in Russia & CIS countries; Not FDA approved Varies; some are prescription, others not

Conclusion

Cerebrolysin is a unique biopharmaceutical agent derived from purified porcine brain tissue through a sophisticated and highly controlled manufacturing process. Its composition of active neuropeptides and amino acids allows it to support the brain through neuroprotection, neuro-regeneration, and enhanced plasticity. While it is an established treatment for stroke, TBI, and dementia in many parts of the world, its lack of FDA approval in the United States makes it an unproven therapy in that context. Its origin story is a testament to the ongoing effort to harness biological processes for therapeutic benefit in neurology.

For more in-depth scientific information, you can review studies on the topic, such as those available through the National Center for Biotechnology Information (NCBI).

Frequently Asked Questions

Cerebrolysin is not an FDA-approved drug in the US and cannot be marketed as a medical treatment. It may be available for personal import or as a research compound, but its legal status for personal use can be ambiguous. It is not available by prescription.

Cerebrolysin is administered parenterally, meaning it bypasses the digestive system. The most common methods are intramuscular (IM) injection, intravenous (IV) injection, or IV infusion.

No, Cerebrolysin is not a steroid. It is a peptide preparation, consisting of naturally derived amino acids and neuropeptides, and does not have a steroidal chemical structure.

Both are peptide-based neurotrophic agents. The main differences are their origin and composition. Cerebrolysin is derived from whole pig brains, while Cortexin is derived from the cerebral cortex of young cattle and pigs. Their exact peptide profiles differ, though they are used for similar indications.

No, Cerebrolysin cannot be taken orally. The peptides would be broken down by digestive enzymes in the stomach and intestines, rendering them ineffective. It must be injected to enter the bloodstream directly.

Cerebrolysin is generally well-tolerated. The most common side effects are mild and transient, such as dizziness, headache, agitation, or a feeling of heat. Injection site reactions like pain or irritation can also occur.

Cerebrolysin is developed, manufactured, and distributed by EVER Neuro Pharma, an Austrian pharmaceutical company that specializes in neurology and critical care.

References

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Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.