Acetylcholinesterase inhibitors (AChE inhibitors) are a class of drugs commonly used in the treatment of Alzheimer's disease. AChE inhibitors work by blocking the enzyme acetylcholinesterase, which is responsible for breaking down the neurotransmitter acetylcholine. By blocking this enzyme, AChE inhibitors result in an increase in the amount of acetylcholine available in the brain, which may improve communication between nerve cells and reduce cognitive decline. AChE inhibitors have been used in the treatment of Alzheimer's for the past few decades. While they can improve some of the symptoms of the disease, their effectiveness is limited. For instance, improvements in memory and thinking often come with side effects such as nausea, vomiting, and diarrhea. Additionally, AChE inhibitors do not slow the progression of Alzheimer's, and their effects may diminish over time. There are several types of AChE inhibitors currently approved for use in the U.S., including donepezil, galantamine, and rivastigmine. These medications are usually prescribed in pill form and taken daily. AChE inhibitors, however, are not recommended for everyone; for instance, they should not be taken if a person has an allergy to any of the ingredients in the drug. Additionally, the drug manufacturer’s instructions should always be followed carefully, as AChE inhibitors are known to interact with other medications. Despite their limitations, AChE inhibitors are generally considered safe and effective medications for the treatment of Alzheimer's disease. They can improve symptoms associated with the disease, and their effects may be long-lasting. As such, AChE inhibitors are important tools in managing this progressive disorder.
Title : Perception and individuality in patient cases identifying the ongoing evolution of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)
Ken Ware, NeuroPhysics Therapy Institute, Australia
Title : Narrative medicine: A communication therapy for the communication disorder of Functional Seizures (FS) [also known as Psychogenic Non-Epileptic Seizures (PNES)]
Robert B Slocum, University of Kentucky HealthCare, United States
Title : Personalized and Precision Medicine (PPM), as a unique healthcare model through biodesign-driven biotech and biopharma, translational applications, and neurology-related biomarketing to secure human healthcare and biosafety
Sergey Victorovich Suchkov, N. D. Zelinskii Institute for Organic Chemistry of the Russian Academy of Sciences, Russian Federation
Title : Neuro sensorium
Luiz Moutinho, University of Suffolk, United Kingdom
Title : GBF1 inhibition reduces amyloid-beta levels in viable human postmortem Alzheimer's disease cortical explant and cortical organoid models
Sean J Miller, Yale School of Medicine, United States
Title : Traumatic Spinal Cord Injuries (tSCI) - Are the radiologically based “advances” in the management of the injured spine evidence-based?
W S El Masri, Keele University, United Kingdom