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Product Usage: This PRODUCT, exclusively offered by Qualitide, is for RESEARCH USE ONLY. It is intended for in vitro testing and laboratory experimentation. All information on this website serves educational purposes only. Introducing this product into humans or animals is illegal. It must be managed by licensed professionals only. This is not a drug, food, or cosmetic and should not be branded or misused as such.
Cerebrolysin is a nootropic drug, which means that it has the capacity to enhance a number of cognitive functions such as memory, concentration, and thinking skills. It is used in the treatment of memory disorders, concentration disorders, and degenerative dementia, including Alzheimer’s disease. Cerebrolysin is also used in the treatment of acute neurological disorders, such as cerebral stroke and craniocerebral trauma. The brain-boosting effects of cerebrolysin may be attributed to the neuropeptides it contains. These neuropeptides are active brain peptides (chains of amino acids) that are used by nerve cells (neurons) to enhance their communication with each other.
Cerebrolysin is a natural compound derived from the brains of pigs using a safe and standardized enzymatic process. In order to achieve its therapeutic effect, cerebrolysin needs to be administered in the form of injections.
Cerebrolysin works by increasing the levels of neurotrophic factors (NFT) and brain-derived neurotrophic factors (BDNF). This in turn stimulates the formation and repair of neurons (nerve cells) in the brain.
There is increasing evidence that cerebrolysin may help improve cognitive function and counter the effects of certain medical conditions that lead to cognitive impairment:
The brain-boosting effect of cerebrolysin also has a beneficial effect on mood, especially in depressive symptoms. Studies show that administration of cerebrolysin produces an antidepressant effect:
Autism, or autism spectrum disorder (ASD), refers to a wide range of medical conditions that affect social interaction, behavior, speech, and nonverbal communication. Since cerebrolysin has the capacity to enhance a number of cognitive functions, this nootropic drug has also been studied for its beneficial effect on autism:
ADHD is a mental disorder characterized by hyperactivity, impulsivity, and short attention span. This mental disorder affects children and teens and can transition into adulthood. Studies show that administration of cerebrolysin may help reduce symptoms of ADHD:
With nerve damage, there can be a broad range of symptoms depending on the location and types of nerves affected. In addition, chronic nerve damage may impair the sensation or function of the affected body part. Interestingly, numerous studies support the therapeutic benefits of cerebrolysin in different medical conditions associated with nerve damage:
Adverse environmental circumstances such as heat stress related to hot climates can lead to disturbed mental function. This condition is known as hyperthermia-induced neurotoxicity. Researchers suggest that one of the suitable therapeutic strategies to treat heat-induced mental anomalies related to this condition is cerebrolysin administration. Studies show that cerebrolysin exerts its therapeutic effect through the following important mechanisms:
Prolonged use of morphine changes the way nerve receptors in the brain work. As a result, sudden withdrawal from this drug can lead to debilitating symptoms such as sleep problems, restlessness, anxiety, digestive problems, high blood pressure, rapid heartbeat, and vision problems. Studies suggest that cerebrolysin can be considered a therapeutic option for morphine withdrawal symptoms:
There is mounting evidence that cerebrolysin may help heighten the immune response and prevent a wide array of diseases. Studies show that cerebrolysin positively affects the production of different cells of the immune system:
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Cerebrolysin has the capacity to stimulate the regeneration of various nerves and cells in the body. Studies show that this regenerative ability may help maintain visual health:
Cerebrolysin side effects are very uncommon, but adverse events have been reported. There is also a potential for serious adverse events with Cerebrolysin use, including an increase in non-fatal serious adverse events. There have been some side effects associated with the use of this drug wherein the patient had one of the issues listed below at some point while being on cerebrolysin. However, these side effects weren’t confirmed to be associated with the treatment and could have been a coincidence and not related to the use of cerebrolysin. Despite this, it was listed as a side effect associated with cerebrolysin even though these associated side effects are very uncommon.
Side effects associated with cerebrolysin may include the following:
Cerebrolysate, commonly known as Cerebrolysin, is a peptide-based, neurotrophic treatment derived from pig brain proteins. It contains a balanced composition of free amino acids and biologically active neuropeptides. The formulation is specifically designed to mimic the natural neurotrophic factors in the human brain that regulate the survival, development, and function of neurons. Cerebrolysin is used extensively in neurology and psychiatry to treat a variety of brain health issues and neurodegenerative disorders, including traumatic brain injury. Reviews in the database of systematic reviews have assessed its efficacy and safety for these applications, often finding little to no difference in outcomes compared to other treatments. Despite its use, some studies have reported little to no difference in clinical improvement between patients treated with Cerebrolysin and those receiving standard care. Continued research and systematic reviews are necessary to further evaluate its potential benefits and to understand why some findings indicate little to no difference in therapeutic efficacy.
The therapeutic action of Cerebrolysate centers on its neuroprotective and neurorestorative effects. It works by enhancing brain metabolism and plasticity, which leads to improved brain function and reduced symptoms in various neurological conditions, such as stroke, traumatic brain injury, Alzheimer’s disease, and other forms of dementia. Research and clinical applications suggest that Cerebrolysate helps improve symptoms in these disorders, offering hope for symptom management and quality of life improvement in patients with conditions like autism, ADHD, and cerebral palsy, as documented in the database of systematic reviews. The inclusion criteria for these studies ensure that only relevant and high-quality research is considered, providing robust evidence for Cerebrolysate’s efficacy. Inclusion criteria also play a crucial role in determining the applicability of findings to different patient populations. Additionally, the inclusion criteria help standardize the assessment of outcomes, facilitating a clearer understanding of the therapeutic benefits of Cerebrolysate across various neurological conditions.
Administration of Cerebrolysate is typically done through injections or infusions, considering it is a peptide that may be broken down if taken orally. The treatment regimen varies depending on the patient’s condition and the severity of symptoms, usually involving a series of doses over a period of time. Effective in managing symptoms of traumatic brain injury, Cerebrolysate’s wide usage and potential benefits are under continuous research to better understand its full scope and mechanism of action within neurotherapeutic applications, particularly for traumatic brain injury. The ability of Cerebrolysate to counteract pathologies associated with traumatic brain injury is a key area of investigation, with numerous entries in the database of systematic reviews supporting its clinical use. Further studies aim to elucidate how Cerebrolysate can counteract pathologies in other neurological conditions. Continued research is crucial to determine how effectively Cerebrolysate can counteract pathologies across various neurotherapeutic applications.
Cerebrolysin, available in 10ml vials among other dosages, is regarded positively in many clinical settings for its potential neuroprotective and neurotrophic effects. It is often administered to improve cognitive function, treat neurodegenerative disorders, and aid recovery in patients suffering from stroke or traumatic brain injuries. Moderate certainty evidence supports its use in these contexts, highlighting its benefits in enhancing cognitive recovery and overall neurological health. The 10ml dosage allows for controlled administration of the treatment, tailored to meet the specific needs and medical conditions of patients, ensuring both efficacy and safety, particularly in those with chronic neurological disorders. Additionally, moderate certainty evidence suggests that Cerebrolysin can be effective in managing symptoms of chronic neurological conditions, contributing to improved patient outcomes. This moderate certainty evidence underscores the importance of dosage control and personalized treatment plans in achieving optimal therapeutic effects with Cerebrolysin.
The effectiveness of the 10ml dosage of Cerebrolysin is supported by various studies, which suggest improvements in symptoms of Alzheimer’s disease, dementia, and other cognitive impairments when used as part of a comprehensive treatment plan for chronic neurological disorders. However, some studies indicate an unclear risk in terms of the consistency of these improvements. Patients often report improvements in memory, focus, and overall cognitive ability, as well as enhanced mood and functionality. Despite these positive reports, there remains an unclear risk regarding the long-term efficacy and safety of Cerebrolysin. Moreover, Cerebrolysin’s ability to promote neuronal growth and repair is a critical aspect of its therapeutic value, potentially slowing the progression of chronic neurological disorders and neurodegenerative diseases, though some findings suggest an unclear risk of bias in the reported outcomes.
However, the use of Cerebrolysin, including the 10ml dosage, is not without concerns, especially in the treatment of chronic neurological disorders. It requires careful handling and administration, typically via injection or infusion, which can be a limitation for some patients. Side effects, although generally mild, can include fatigue, headache, and dizziness. As with any medical treatment, the decision to use Cerebrolysin should be made in consultation with a healthcare provider, taking into account the individual’s medical history and specific health needs related to chronic neurological disorders. Overall, while Cerebrolysin 10ml has demonstrated beneficial effects for many, its suitability and effectiveness can vary depending on the patient and the condition being treated.
The price of Cerebrolysin can vary widely depending on several factors, including the country of purchase, the purchasing source (hospital, pharmacy, or online distributor), and the dosage form. Generally, Cerebrolysin is considered a premium medication, primarily due to its complex manufacturing process and the biological origin of its ingredients. It is typically more expensive in regions where it is not widely distributed or where medical treatments tend to have higher overall costs, particularly when used for conditions like acute ischemic stroke. However, the efficacy of Cerebrolysin in treating acute ischemic stroke is based on low certainty evidence, which impacts the overall perceived value of the treatment. The need for acute ischemic stroke treatments such as Cerebrolysin emphasizes its value despite higher costs, even though the supporting data is often of low certainty evidence. Further research and systematic reviews are necessary to strengthen the evidence base, as current findings are often characterized by low certainty evidence, influencing both clinical decisions and healthcare costs.
In terms of specific costs, the price of a 10ml vial of Cerebrolysin can range significantly. For example, in the United States and Western Europe, prices are typically higher due to regulatory practices and market conditions. In contrast, in Eastern European countries, where Cerebrolysin is more commonly used and locally produced, especially for treating acute ischemic stroke, the prices can be somewhat lower. Online pharmacies might offer competitive pricing, but buyers should be cautious of the source to ensure they are obtaining a legitimate and safe product for acute ischemic stroke treatment. The potential benefit for acute ischemic stroke recovery can justify the effort and expense of sourcing Cerebrolysin.
The price of Cerebrolysin can vary widely depending on several factors, including the country of purchase, the purchasing source (hospital, pharmacy, or online distributor), and the dosage form. Generally, Cerebrolysin is considered a premium medication, primarily due to its complex manufacturing process and the biological origin of its ingredients. It is typically more expensive in regions where it is not widely distributed or where medical treatments tend to have higher overall costs, particularly when used for conditions like acute ischemic stroke. However, the efficacy of Cerebrolysin in treating acute ischemic stroke is based on low certainty evidence, which impacts the overall perceived value of the treatment. The need for acute ischemic stroke treatments such as Cerebrolysin emphasizes its value despite higher costs, even though the supporting data is often of low certainty evidence. Further research and systematic reviews are necessary to strengthen the evidence base, as current findings are often characterized by low certainty evidence, influencing both clinical decisions and healthcare costs.
Cortexin® and Cerebrolysin® are both peptide-based drugs used primarily in neurology for their neuroprotective and neurotrophic effects, but they have distinct compositions and slightly different applications. Cortexin® is derived from the cerebral cortex of pigs and contains a complex of polypeptide fractions along with amino acids that influence the central nervous system. It is administered to improve brain function, protect against damage, and enhance recovery from various neurological conditions. Unlike Cerebrolysin, which is derived from pig brain proteins and contains a mixture of low-molecular-weight peptides and free amino acids, Cortexin’s active components are smaller and potentially more focused in their action.
In terms of clinical use, both Cortexin® and Cerebrolysin are utilized to treat similar conditions, including traumatic brain injuries, stroke recovery, and cognitive disorders such as Alzheimer’s disease. However, the specific indications and the perceived efficacy can vary. Cortexin is often noted for its neuroprotective properties and its ability to stabilize cell membranes and reduce oxidative stress. Cerebrolysin, on the other hand, is more explicitly recognized for its role in enhancing cognitive functions and supporting neuronal growth and repair, making it particularly useful in the treatment of dementia and similar degenerative conditions.
The choice between Cortexin® and Cerebrolysin often comes down to clinical objectives, patient response to treatment, and the preferences of the healthcare provider. Both medications are administered via injection, requiring similar protocols for use. Side effects for both drugs are generally mild but can include discomfort at the injection site, dizziness, and headaches. While both treatments are supported by a substantial amount of research, the body of evidence is more robust for Cerebrolysin, particularly in its effects on a broad range of neurodegenerative and cognitive disorders, as documented in the database of systematic reviews. Ultimately, the decision to use Cortexin or Cerebrolysin should be tailored to the individual patient’s condition and needs, often guided by the experience and observation of their healthcare team. Consulting the database of systematic reviews can provide valuable insights into the comparative efficacy and safety of these treatments. Additionally, continuous reference to the database of systematic reviews helps ensure that treatment decisions are based on the most comprehensive and up-to-date evidence available.
Cerebrolysin has garnered attention in the medical community for its potential therapeutic effects in treating stroke and vascular dementia. This peptide-based treatment is believed to confer neuroprotective and neurotrophic benefits, making it a viable option for promoting neural repair and functional recovery post-stroke. The neurotrophic factors present in Cerebrolysin are thought to enhance neurogenesis, reduce inflammation, and improve synaptic connectivity, which can be critical in the acute phase following a stroke. Clinical trials and studies have shown that when administered soon after a stroke, Cerebrolysin can help improve neurological function and reduce the extent of brain damage, with a low incidence of serious adverse events.
In the context of vascular dementia, Cerebrolysin’s ability to improve cognitive functions and protect neural structures offers a promising approach to managing this condition. Vascular dementia, which results from impaired blood flow to the brain leading to cognitive decline, can benefit from Cerebrolysin’s mechanisms that enhance cerebral blood flow and neuronal resilience. Patients treated with Cerebrolysin have reported improvements in memory, attention, and executive function. Continuous research and clinical trials suggest that Cerebrolysin not only helps in stabilizing the symptoms of vascular dementia but may also slow its progression, offering a better quality of life for patients, with minimal serious adverse events.
Despite the promising outcomes, the use of Cerebrolysin in stroke recovery and vascular dementia must be carefully considered by healthcare professionals. The treatment involves a series of injections or infusions, which require monitoring and management by medical personnel. Side effects, though generally mild, can include headache, nausea, and dizziness. The risk of serious adverse events, while low, requires careful monitoring. Reviews in the Cochrane Database of Systematic Reviews highlight the importance of such vigilance in clinical practice. The cost of treatment and the variability in patient responses also pose challenges. Therefore, while Cerebrolysin offers a potentially effective treatment modality for stroke and vascular dementia, it should be part of a comprehensive therapeutic plan that includes other medical interventions and lifestyle adjustments tailored to individual patient needs. Ongoing vigilance for any serious adverse events is critical, as emphasized by findings from the Cochrane Database of Systematic Reviews. Additionally, systematic reviews and meta-analyses, such as those found in the Cochrane Database of Systematic Reviews, provide valuable insights into the efficacy and safety of Cerebrolysin, guiding healthcare professionals in making informed decisions about its use in diverse patient populations.
Purchasing Cerebrolysin online is a convenient option for many, offering the ability to source this treatment from various global suppliers. However, potential buyers should proceed with caution. Cerebrolysin requires precise storage conditions to maintain its efficacy and safety, such as specific temperature ranges which might not be guaranteed during international shipping. Additionally, the authenticity of the product is crucial as counterfeit medications can pose significant health risks. Buyers should seek out reputable pharmacies or distributors that provide clear product sourcing information and have good reviews from other users, potentially verified through resources like the Cochrane Database of Systematic Reviews. It’s important to reference the Cochrane Database of Systematic Reviews for verified information on product efficacy and safety, as this resource is known for its rigorous assessment of clinical trials and treatments. Finally, consulting the Cochrane Database of Systematic Reviews can help ensure that the purchased Cerebrolysin meets high standards and has been evaluated in reliable studies.
Before buying Cerebrolysin online, it’s important to verify the legal implications of importing prescription drugs into your country. Regulations can vary widely; some countries strictly prohibit importing drugs without a local prescription, while others may allow it under certain conditions. Consulting with a healthcare professional is also recommended to ensure that Cerebrolysin is an appropriate treatment option for your condition. They can provide guidance on the correct dosage and administration, and monitor treatment progress and safety, with standards often reflected in the Cochrane database of systematic reviews.
Additionally, price comparisons can reveal significant differences in cost, which can be influenced by factors like origin of manufacture, shipping fees, and import taxes. Websites offering extremely low prices should be approached with suspicion as they may be selling counterfeit or expired products. Secure payment options and a clear return policy are also important to consider when purchasing medications online, with the Cochrane database of systematic reviews often providing data on efficacy and safety that can help guide purchasing decisions. Ultimately, while the convenience of buying Cerebrolysin online is appealing, ensuring the safety and legality of the purchase should be the top priority, supported by evidence from the Cochrane database of systematic reviews.
Xiao S, Xue H, Li G. Therapeutic effects of cerebrolysin added to risperidone in patients with schizophrenia dominated by negative symptoms. The Australian and New Zealand journal of psychiatry. 2012; 46(2):153-60. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22311531
Crook TH, Ferris SH, Alvarez XA, Laredo M, Moessler H. Effects of N-PEP-12 on memory among older adults. International clinical psychopharmacology. 2005; 20(2):97-100. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/15729085
Alvarez XA, Lombardi VR, Corzo L. Oral Cerebrolysin enhances brain alpha activity and improves cognitive performance in elderly control subjects. Journal of neural transmission. Supplementum. 2000; 59:315-28. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/10961443
Allegri RF, Guekht A. Cerebrolysin improves symptoms and delays progression in patients with Alzheimer’s disease and vascular dementia. Drugs of today (Barcelona, Spain: 1998). 2012; 48 Suppl A:25-41. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22514793
Rockenstein E, Torrance M, Mante M. Cerebrolysin decreases amyloid-beta production by regulating amyloid protein precursor maturation in a transgenic model of Alzheimer’s disease. Journal of neuroscience research. 2006; 83(7):1252-61. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/16511867
Rockenstein E, Mallory M, Mante M. Effects of Cerebrolysin on amyloid-beta deposition in a transgenic model of Alzheimer’s disease. Journal of neural transmission. Supplementum. 2002. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/12456076.
Rockenstein E, Adame A, Mante M, Moessler H, Windisch M, Masliah E. The neuroprotective effects of Cerebrolysin in a transgenic model of Alzheimer’s disease are associated with improved behavioral performance. Journal of neural transmission (Vienna, Austria : 1996). 2003; 110(11):1313-27. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/14628195
Ladurner G, Kalvach P, Moessler H, .Neuroprotective treatment with cerebrolysin in patients with acute stroke: a randomised controlled trial. Journal of neural transmission (Vienna, Austria : 1996). 2005; 112(3):415-28. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/15583955
Muresanu DF, Heiss W-D, Hoemberg V, et al. Cerebrolysin and Recovery After Stroke (CARS): A Randomized, Placebo-Controlled, Double-Blind, Multicenter Trial. Stroke; a Journal of Cerebral Circulation. 2016;47(1):151-159. doi:10.1161/STROKEAHA.115.009416. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4689177/.
Guekht A, Vester J, Heiss WD. Safety and efficacy of Cerebrolysin in motor function recovery after stroke: a meta-analysis of the CARS trials. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2017; 38(10):1761-1769. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28707130.
Chen CC, Wei ST, Tsaia SC, Chen XX, Cho DY. Cerebrolysin enhances cognitive recovery of mild traumatic brain injury patients: double-blind, placebo-controlled, randomized study. British journal of neurosurgery. 2013; 27(6):803-7. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/23656173.
Bornstein N, Poon WS. Accelerated recovery from acute brain injuries: clinical efficacy of neurotrophic treatment in stroke and traumatic brain injuries. Drugs of today (Barcelona, Spain : 1998). 2012; 48 Suppl A:43-61. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22514794
Wong GK, Zhu XL, Poon WS. Beneficial effect of cerebrolysin on moderate and severe head injury patients: result of a cohort study. Actaneurochirurgica. Supplement. 2005; 95:59-60. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/16463821.
Zhang D, Dong Y, Li Y, Chen J, Wang J, Hou L. Efficacy and Safety of Cerebrolysin for Acute Ischemic Stroke: A Meta-Analysis of Randomized Controlled Trials. BioMed Research International. 2017;2017:4191670. doi:10.1155/2017/4191670. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5474547/.
Hassanein SM, Deifalla SM, El-Houssinie M, Mokbel SA. Safety and Efficacy of Cerebrolysin in Infants with Communication Defects due to Severe Perinatal Brain Insult: A Randomized Controlled Clinical Trial. Journal of clinical neurology (Seoul, Korea). 2016; 12(1):79-84. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/26365023.
Ozkizilcik A, Sharma A, Muresanu DF. Timed Release of Cerebrolysin Using Drug-Loaded TitanateNanospheres Reduces Brain Pathology and Improves Behavioral Functions in Parkinson’s Disease. Molecular neurobiology. 2017. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28875428.
Ozkizilcik A, Sharma A, Muresanu DF. Timed Release of Cerebrolysin Using Drug-Loaded TitanateNanospheres Reduces Brain Pathology and Improves Behavioral Functions in Parkinson’s Disease. Molecular neurobiology. 2017. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28875428.
Requejo C, Ruiz-Ortega JA, Cepeda H. Nanodelivery of Cerebrolysin and Rearing in Enriched Environment Induce Neuroprotective Effects in a Preclinical Rat Model of Parkinson’s Disease. Molecular neurobiology. 2017. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28840482.
Noor NA, Mohammed HS, Mourad IM, Khadrawy YA, AboulEzz HS. A promising therapeutic potential of cerebrolysin in 6-OHDA rat model of Parkinson’s disease. Life sciences. 2016; 155:174-9. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/27210889
KalynIaB, Safarova TP, Sheshenin VC, Gavrilova SI. [Comparative efficacy and safety of antidepressant mono- and multimodal therapy in elderly patients with depression (a clinical experience in a psychogeriatric hospital)]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 2014; 114(6 Pt 2):20-9. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/25042499.
Gharagozli, K., Harandi, A. A., Houshmand, S., Akbari, N., Muresanu, D. F., Vester, J., Winter, S., & Moessler, H. (2017). Efficacy and safety of Cerebrolysin treatment in early recovery after acute ischemic stroke: a randomized, placebo-controlled, double-blinded, multicenter clinical trial. Journal of medicine and life, 10(3), 153–160.
Masliah, E., & Díez-Tejedor, E. (2012). The pharmacology of neurotrophic treatment with Cerebrolysin: brain protection and repair to counteract pathologies of acute and chronic neurological disorders. Drugs of today (Barcelona, Spain: 1998), 48 Suppl A, 3–24. https://doi.org/10.1358/dot.2012.48(Suppl.A).1739716
Fiani, B., Covarrubias, C., Wong, A., Doan, T., Reardon, T., Nikolaidis, D., & Sarno, E. (2021). Cerebrolysin for stroke, neurodegeneration, and traumatic brain injury: review of the literature and outcomes. Neurological sciences: official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 42(4), 1345–1353. https://doi.org/10.1007/s10072-021-05089-2
Zhang, C., Chopp, M., Cui, Y., Wang, L., Zhang, R., Zhang, L., Lu, M., Szalad, A., Doppler, E., Hitzl, M., & Zhang, Z. G. (2010). Cerebrolysin enhances neurogenesis in the ischemic brain and improves functional outcome after stroke. Journal of neuroscience research, 88(15), 3275-3281. https://doi.org/10.1002/jnr.22495.
Bornstein, N. M., Guekht, A., Vester, J., Heiss, W. D., Gusev, E., Hömberg, V., Rahlfs, V. W., Bajenaru, O., Popescu, B. O., & Muresanu, D. (2018). Safety and efficacy of Cerebrolysin in early post-stroke recovery: a meta-analysis of nine randomized clinical trials. Neurological sciences: official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 39(4), 629–640. https://doi.org/10.1007/s10072-017-3214-0.
Heiss, W. D., Brainin, M., Bornstein, N. M., Tuomilehto, J., Hong, Z., & Cerebrolysin Acute Stroke Treatment in Asia (CASTA) Investigators (2012). Cerebrolysin in patients with acute ischemic stroke in Asia: results of a double-blind, placebo-controlled randomized trial. Stroke, 43(3), 630–636. https://doi.org/10.1161/STROKEAHA.111.628537.
Chang, W. H., Lee, J., Shin, Y. I., Ko, M. H., Kim, D. Y., Sohn, M. K., Kim, J., & Kim, Y. H. (2021). Cerebrolysin Combined with Rehabilitation Enhances Motor Recovery and Prevents Neural Network Degeneration in Ischemic Stroke Patients with Severe Motor Deficits. Journal of personalized medicine, 11(6), 545. https://doi.org/10.3390/jpm11060545
Tran, L., Alvarez, X. A., Le, H. A., Nguyen, D. A., Le, T., Nguyen, N., Nguyen, T., Nguyen, T., Vo, T., Tran, T., Duong, C., Nguyen, H., Nguyen, S., Nguyen, H., Le, T., Nguyen, M., & Nguyen, T. (2022). Clinical Efficacy of Cerebrolysin and Cerebrolysin plus Nootropics in the Treatment of Patients with Acute Ischemic Stroke in Vietnam. CNS & neurological disorders drug targets, 21(7), 621–630. https://doi.org/10.2174/1871527320666210820091655
Stan, A., Birle, C., Blesneag, A., & Iancu, M. (2017). Cerebrolysin and early neurorehabilitation in patients with acute ischemic stroke: a prospective, randomized, placebo-controlled clinical study. Journal of medicine and life, 10(4), 216–222.
Chen, N., Yang, M., Guo, J., Zhou, M., Zhu, C., & He, L. (2013). Cerebrolysin for vascular dementia. The Cochrane database of systematic reviews, (1), CD008900. https://doi.org/10.1002/14651858.CD008900.pub2.
Lang, W., Stadler, C. H., Poljakovic, Z., Fleet, D., & Lyse Study Group (2013). A prospective, randomized, placebo-controlled, double-blind trial about safety and efficacy of combined treatment with alteplase (rt-PA) and Cerebrolysin in acute ischaemic hemispheric stroke. International journal of stroke: official journal of the International Stroke Society, 8(2), 95–104. https://doi.org/10.1111/j.1747-4949.2012.00901.x.
Panisset M, Gauthier S, Moessler H, Windisch M, .Cerebrolysin in Alzheimer’s disease: a randomized, double-blind, placebo-controlled trial with a neurotrophic agent. Journal of neural transmission (Vienna, Austria: 1996). 2002; 109(7-8):1089-104. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/12111446.
Retrieved from http://www.wfsbp.org/doi/wfsbp2011-abstractscd/en/abstracts/10025.html.
Shabanov PD, Lebedev AA, Pavlenko VP, Ganapol’skiĭ VP. [Comparative study of behavioral effects of cortexin and cerebrolysine upon intraventricular and intraperitoneal administration in rats]. Eksperimental’naia i klinicheskaiafarmakologiia. ; 70(3):13-9. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/17650626
Krasnoperova MG, Bashina VM, Skvortsov IA, Simashkova NV. [The effect of cerebrolysin on cognitive functions in childhood autism and in Asperger syndrome]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 2003; 103(6):15-8. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/12872620.
Chutko LS, Yakovenko EA, Surushkina SY, Kryukova EM, Palaieva SV. [The efficacy of cerebrolysin in the treatment of autism spectrum disorders]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 2017; 117(9):71-75. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/29053124.
Cuevas-Olguin R, Roychowdhury S, Banerjee A. Cerebrolysin prevents deficits in social behavior, repetitive conduct, and synaptic inhibition in a rat model of autism. Journal of neuroscience research. 2017; 95(12):2456-2468. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28609577.
Sotnikova NY, Gromova OA, Novicova EA. Dual effect of cerebrolysin in children with attention deficit syndrome with hyperactivity: neuroprotection and immunomodulation. Russian journal of immunology: RJI : official journal of Russian Society of Immunology. 2002; 7(4):357-64. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/12687248
Chutko LS, Yakovenko EA, Surushkina SY, Anisimova TI, Kropotov YD. [Clinical and neurophysiological heterogeneity of attention deficit hyperactivity disorder]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova.; 116(10):117-121. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/27845323.
Nasiri J, Safavifar F. Effect of cerebrolysin on gross motor function of children with cerebral palsy: a clinical trial. ActaneurologicaBelgica. 2017; 117(2):501-505. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/28074392.
Gershman RN, Vasilenko MA. [Use of cerebrolysin and ATP in treating infantile cerebral paralysis]. Pediatriiaakusherstvo i ginekologiia.. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/1228606.
Retrieved from https://cerebralpalsynewstoday.com/2017/06/07/cerebrolysin-can-help-improve-motor-skills-in-cerebral-palsy-patients/.
Retrieved from https://clinicaltrials.gov/ct2/show/NCT02116348
Biesenbach G, Grafinger P, Eichbauer-Sturm G, Zazgornik J. [Cerebrolysin in treatment of painful diabetic neuropathy]. Wiener medizinischeWochenschrift (1946). 1997; 147(3):63-6. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9173675.
Dong H, Jiang X, Niu C, Du L, Feng J, Jia F. Cerebrolysin improves sciatic nerve dysfunction in a mouse model of diabetic peripheral neuropathy. Neural Regeneration Research. 2016;11(1):156-162. doi:10.4103/1673-5374.175063. Retrieved from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774211/
Masliah E, Armasolo F, Veinbergs I, Mallory M, Samuel W. Cerebrolysin ameliorates performance deficits, and neuronal damage in apolipoprotein E-deficient mice. Pharmacology, biochemistry, and behavior. 1999; 62(2):239-45. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9972690.
Keilhoff G, Lucas B, Pinkernelle J, Steiner M, Fansa H. Effects of cerebrolysin on motor-neuron-like NSC-34 cells. Experimental cell research. 2014; 327(2):234-55. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/24997385.
Shchudlo NA, Shchudlo MM, Borisova IV. [The effect of cerebrolysin on the regeneration of the peripheral nerve depending on the scheme of paraneural administration]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 2013; 113(12):76-80. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/24430040.
Available from https://journals.lww.com/nrronline/Abstract/2011/06180/Cerebrolysin_as_a_nerve_growth_factor_for.10.aspx.
Sharma HS, Sharma A, Mössler H, Muresanu DF. Neuroprotective effects of cerebrolysin, a combination of different active fragments of neurotrophic factors and peptides on the whole body hyperthermia-induced neurotoxicity: modulatory roles of co-morbidity factors and nanoparticle intoxication. International review of neurobiology. 2012; 102:249-76. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22748833.
Sharma A, Muresanu DF, Mössler H, Sharma HS. Superior neuroprotective effects of cerebrolysin in nanoparticle-induced exacerbation of hyperthermia-induced brain pathology. CNS & neurological disorders drug targets. 2012; 11(1):7-25. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22229316.
Martínez-Laorden E, Hurle MA, Milanés MV, Laorden ML, Almela P. Morphine withdrawal activates hypothalamic-pituitary-adrenal axis and heat shock protein 27 in the left ventricle: the role of extracellular signal-regulated kinase. The Journal of pharmacology and experimental therapeutics. 2012; 342(3):665-75. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/22647273.
Sharma HS, Ali SF, Patnaik R, Zimmermann-Meinzingen S, Sharma A, Muresanu DF. Cerebrolysin Attenuates Heat Shock Protein (HSP 72 KD) Expression in the Rat Spinal Cord Following Morphine Dependence and Withdrawal: Possible New Therapy for Pain Management. Current neuropharmacology. 2011; 9(1):223-35. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/21886595.
Belokrylov GA, Malchanova IV. [Levamin and cerebrolysin as immunostimulants]. Biulleten’ eksperimental’noibiologii i meditsiny. 1992; 113(2):165-6. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/1611065.
Govorin NV, Zlova TP, Akhmetova VV, Tarasova OA. [The pathophysiological analysis of cerebrolysin therapy of children with mental developmental delay caused by ecological factors]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 2008; 108(5):51-5. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/18577958.
Sotnikova NY, Gromova OA, Novikova EA, Burtsev EM. Immunoactive Properties of Cerebrolysin. Russian journal of immunology: RJI : official journal of Russian Society of Immunology. 2000; 5(1):63-70. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/12687163.
Garmanchuk LV, Perepelitsyna EM, SidorenkoMv, Makarenko AN, Kul’chikov AE. [Cytoprotective effect of neuropeptides on immunocompetent cells (in vitro study)]. Eksperimental’naia i klinicheskaiafarmakologiia.; 72(4):28-32. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/19803367
González ME, Francis L, Castellano O. Antioxidant systemic effect of short-term Cerebrolysin administration. Journal of neural transmission. Supplementum. 1998; 53:333-41. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9700669.
Gromova OA, Avdeenko TV, Burtsev EM, Skal’nyĭ AV, Solov’ev OI. [Effects of cerebrolysin on the oxidant homeostasis, the content of microelements and electrolytes in children with minimal brain dysfunction]. Zhurnalnevrologii i psikhiatriiimeni S.S. Korsakova. 1998; 98(1):27-30. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9505400.
González ME, Francis L, Castellano O. Antioxidant systemic effect of short-term Cerebrolysin administration. Journal of neural transmission. Supplementum. 1998; 53:333-41. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/9700669.
Retrieved from http://europepmc.org/abstract/med/9505400.
Huang TL, Huang SP, Chang CH, Lin KH, Sheu MM, Tsai RK. Protective effects of cerebrolysin in a rat model of optic nerve crush. The Kaohsiung journal of medical sciences. 2014; 30(7):331-6. Retrieved from https://www.ncbi.nlm.nih.gov/pubmed/24924838.
Retrieved from http://www.roneurosurgery.eu/atdoc/16CostinDCombined.pdf.
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