Research, Articles & Case Studies

In the latest research published in the journal Neuron, scientists led by John Gabrieli, a professor of brain and cognitive sciences at Massachusetts Institute of Technology, found that dyslexia may be due to a much broader difference in brain function. 

But in the latest research published in the journal Neuron, scientists led by John Gabrieli, a professor of brain and cognitive sciences at Massachusetts Institute of Technology, found that dyslexia may be due to a much broader difference in brain function. 

Background: Apolipoprotein E (apoE) is a major carrier of cholesterol and essential for synaptic plasticity. In brain, it’s expressed by many cells but highly expressed by the choroid plexus and the predominant apolipoprotein in cerebrospinal fluid (CSF). The role of apoE in the CSF is unclear. Recently, the glymphatic system was described as a clearance system whereby CSF and ISF (interstitial fluid) is exchanged via the peri-arterial space and convective flow of ISF clearance is mediated by aquaporin 4 (AQP4), a water channel. We reasoned that this system also serves to distribute essential molecules in CSF into brain. The aim was to establish whether apoE in CSF, secreted by the choroid plexus, is distributed into brain, and whether this distribution pattern was altered by sleep deprivation. Methods: We used fluorescently labeled lipidated apoE isoforms, lenti-apoE3 delivered to the choroid plexus, immunohistochemistry to map apoE brain distribution, immunolabeled cells and proteins in brain, Western blot analysis and ELISA to determine apoE levels and radiolabeled molecules to quantify CSF inflow into brain and brain clearance in mice. Data were statistically analyzed using ANOVA or Student’s t- test. Results: We show that the glymphatic fluid transporting system contributes to the delivery of choroid plexus/ CSF-derived human apoE to neurons. CSF-delivered human apoE entered brain via the perivascular space of penetrating arteries and flows radially around arteries, but not veins, in an isoform specific manner (apoE2 > apoE3 > apoE4). Flow of apoE around arteries was facilitated by AQP4, a characteristic feature of the glymphatic system. ApoE3, delivered by lentivirus to the choroid plexus and ependymal layer but not to the parenchymal cells, was present in the CSF, penetrating arteries and neurons. The inflow of CSF, which contains apoE, into brain and its clearance from the interstitium were severely suppressed by sleep deprivation compared to the sleep state. Conclusions: Thus, choroid plexus/CSF provides an additional source of apoE and the glymphatic fluid transporting system delivers it to brain via the periarterial space. By implication, failure in this essential physiological role of the glymphatic fluid flow and ISF clearance may also contribute to apoE isoform-specific disorders in the long term.

This article talks about positive body talk for healing.

Ehlers-Danlos Syndrome is a genetic, connective tissue disorder affecting collagen production. One of the primary and most debilitating symptoms of EDS is a widespread, unrelenting and varying pain, with episodes of acute, excruciating pain when there is a direct joint injury, subluxation, or dislocation.   Many people with EDS do not realize they have it. 

Ken Koles talks about what Craniosacral Therapy is and the benefits of this work. 

This article is about how unexpected cells have been found in the protective membranes that enclose the brain, the so called meninges. These 'neural progenitors' -- or stem cells that differentiate into different kinds of neurons-- are produced during embryonic development. These findings show that the neural progenitors found in the meninges produce new neurons after birth-- highlighting the importance of meningeal tissue as well as these cells' potential in the development of new therapies for brain damage and neurodegeneration. A paper highlighting the results was published in the leading scientific journal Cell Stem Cell.

Abstract 

Introduction: Trigeminal Neuralgia {TN) can be an extremely debilitating condition effecting quality of life, emotional well-being, and engagement in daily occupation. Surgical and medication treatments are cited extensively through the literature but can have undesired side effects, can lose effectiveness over time, or are quite invasive. Little is reported about craniosacral therapy, lymphatic drainage, or other gentle manual techniques as treatment options. 

Objective: This paper introduces and summarizes the experiential process and outcomes of three adults receiving manual therapies to treat TN. This review investigates low-risk, conservation clinical options and explores for treatment guidelines for TN. 

Method: Chart review and client interviews in multiple follow-up contacts of a convenience sample to explore immediate and long term outcomes. All treatment techniques utilized per clients are summarized, and include: Upledger's CranioSacral Therapy (U-CST); Chikly's brain curriculum for lymphatic enhancement and nerve down-regulation techniques; and Wanveer's glia structure and glymphatic mobilization techniques. One occurrence of a spontaneous Somato-Emotional Release technique was also called for. Measurement of baseline and outcomes was conducted using: Verbal descriptor scale; Verbal numeric rating scale; Visual analog scale (VAS); and Self-report of quality of life and pain's impact upon performing daily activities. Data were analyzed using qualitative content analysis 

Conclusion: Three adults reported individual positive changes or resolution of TN pain. All three reported restoration of quality of life and emotional well-being. One made use of techniques for self-help Comparison to other methods, or variations of these methods utilizing the same names or terminologies, should be avoided. This report is an attempt to aid in the needed clarification between different approaches used in clinical practices. Positive responses suggest that these methods hold value for further study as a viable treatment option to address the agony of neuralgia.