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1.
Int J Mol Sci ; 24(23)2023 Nov 28.
Article in English | MEDLINE | ID: mdl-38069179

ABSTRACT

Brain remodeling after an ischemic stroke represents a promising avenue for exploring the cellular mechanisms of endogenous brain repair. A deeper understanding of these mechanisms is crucial for optimizing the safety and efficacy of neuroprotective treatments for stroke patients. Here, we interrogated the role of extracellular vesicles, particularly exosomes, as potential mediators of endogenous repair within the neurovascular unit (NVU). We hypothesized that these extracellular vesicles may play a role in achieving transient stroke neuroprotection. Using the established ischemic stroke model of middle cerebral artery occlusion in adult rats, we detected a surged in the extracellular vesicle marker CD63 in the peri-infarct area that either juxtaposed or co-localized with GFAP-positive glial cells, MAP2-labeled young neurons, and VEGF-marked angiogenic cells. This novel observation that CD63 exosomes spatially and temporally approximated glial activation, neurogenesis, and angiogenesis suggests that extracellular vesicles, especially exosomes, contribute to the endogenous repair of the NVU, warranting exploration of extracellular vesicle-based stroke therapeutics.


Subject(s)
Brain Ischemia , Extracellular Vesicles , Ischemic Stroke , Stroke , Humans , Rats , Animals , Brain , Infarction, Middle Cerebral Artery
2.
Int J Mol Sci ; 24(19)2023 Sep 27.
Article in English | MEDLINE | ID: mdl-37834059

ABSTRACT

Traumatic brain injury (TBI) results from direct penetrating and indirect non-penetrating forces that alters brain functions, affecting millions of individuals annually. Primary injury following TBI is exacerbated by secondary brain injury; foremost is the deleterious inflammatory response. One therapeutic intervention being increasingly explored for TBI is hyperbaric oxygen therapy (HBOT), which is already approved clinically for treating open wounds. HBOT consists of 100% oxygen administration, usually between 1.5 and 3 atm and has been found to increase brain oxygenation levels after hypoxia in addition to decreasing levels of inflammation, apoptosis, intracranial pressure, and edema, reducing subsequent secondary injury. The following review examines recent preclinical and clinical studies on HBOT in the context of TBI with a focus on contributing mechanisms and clinical potential. Several preclinical studies have identified pathways, such as TLR4/NF-kB, that are affected by HBOT and contribute to its therapeutic effect. Thus far, the mechanisms mediating HBOT treatment have yet to be fully elucidated and are of interest to researchers. Nonetheless, multiple clinical studies presented in this review have examined the safety of HBOT and demonstrated the improved neurological function of TBI patients after HBOT, deeming it a promising avenue for treatment.


Subject(s)
Brain Injuries, Traumatic , Brain Injuries , Hyperbaric Oxygenation , Humans , Hyperbaric Oxygenation/methods , Brain Injuries, Traumatic/therapy , Brain Injuries/therapy , Brain , Oxygen
3.
J Eat Disord ; 10(1): 13, 2022 Feb 05.
Article in English | MEDLINE | ID: mdl-35123579

ABSTRACT

BACKGROUND: Anorexia nervosa (AN) is a disorder characterized by an incapacitating fear of weight gain and by a disturbance in the way the body is experienced, facets that motivate dangerous weight loss behaviors. Multimodal neuroimaging studies highlight atypical neural activity in brain networks involved in interoceptive awareness and reward processing. METHODS: The current study used resting-state neuroimaging to model the architecture of large-scale functional brain networks and characterize network properties of individual brain regions to clinical measures. Resting-state neuroimaging was conducted in 62 adolescents, 22 (21 female) with a history of AN and 40 (39 female) healthy controls (HCs). Sensorimotor and basal ganglia regions, as part of a 165-region whole-brain network, were investigated. Subject-specific functional brain networks were computed to index centrality. A contrast analysis within the general linear model covarying for age was performed. Correlations between network properties and behavioral measures were conducted (significance q < .05). RESULTS: Compared to HCs, AN had lower connectivity from sensorimotor regions, and greater connectivity from the left caudate nucleus to the right postcentral gyrus. AN demonstrated lower sensorimotor centrality, but higher basal ganglia centrality. Sensorimotor connectivity dyads and centrality exhibited negative correlations with body dissatisfaction and drive for thinness, two essential features of AN. CONCLUSIONS: These findings suggest that AN is associated with greater communication from the basal ganglia, and lower information propagation in sensorimotor cortices. This is consistent with the clinical presentation of AN, where individuals exhibit patterns of rigid habitual behavior that is not responsive to bodily needs, and seem "disconnected" from their bodies.


Individuals with anorexia nervosa (AN) usually report a fear of gaining weight. They often develop a dislike and distrust of their bodies, feeling that their bodies had somehow let them down. These fears can in turn lead to dangerous weight loss behaviors. Magnetic resonance imaging of the brain is a tool that helps highlight the underlying biological processes associated with AN. In the current study we aim to investigate how the connections in key regions of the brain are related to clinical and behavioral factors associated with AN. We found regions of two main networks were associated with body dissatisfaction and drive for thinness, which are key features of AN. The brain regions involved help explain why patients with AN have characteristics of feeling disconnected from their bodies, having difficulty labeling and regulating emotions, responding to biological needs such as hunger and fatigue, and differentiating experiences that will be rewarding. These results can help guide interventions that will be directed towards helping individuals with AN to better sense, decipher, and act on the various signals being communicated by their body.

7.
J Reconstr Microsurg ; 27(7): 397-402, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21717398

ABSTRACT

The loss of a free flap is a feared complication for both the surgeon and the patient. Early recognition of vascular compromise has been shown to provide the best chance for flap salvage. The ideal monitoring technique for perioperative free flap ischemia would be noninvasive, continuous, and reliable. Visible light spectroscopy (VLS) was evaluated as a new method for predicting ischemia in microvascular cutaneous soft tissue free flaps. In an Institutional Review Board-approved prospective trial, 12 patients were monitored after free flap reconstructions. The tissue hemoglobin oxygen saturation (StO (2)) and total hemoglobin concentration (THB) of 12 flaps were continuously monitored using VLS for 72 hours postoperatively. Out of these 12 flaps 11 were transplanted successfully and 1 flap loss occurred. The StO (2 )was 48.99% and the THB was 46.74% for the 12 flaps. There was no significant difference in these values among the flaps. For the single flap loss, the device accurately reflected the ischemic drop in StO (2) indicating drastic tissue ischemia at 6 hours postoperatively before the disappearance of implantable Doppler signals or clinical signs of flap compromise. VLS, a continuous, noninvasive, and localized method to monitor oxygenation, appeared to predict early ischemic complications after free flap reconstruction.


Subject(s)
Free Tissue Flaps/blood supply , Ischemia/diagnosis , Oximetry/methods , Oxygen/metabolism , Spectrum Analysis/methods , Adult , Aged , Aged, 80 and over , Graft Survival , Hemoglobins/metabolism , Humans , Middle Aged , Prospective Studies
9.
J Am Acad Dermatol ; 59(1): 137-9, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18329131

ABSTRACT

BACKGROUND: The pathogenesis of alopecia areata (AA) is incompletely known. A positive family history in some points to a genetic predisposition, and discordance of the disease in identical twins suggests environmental triggers exist. OBJECTIVE: We sought to determine whether the Epstein-Barr virus (EBV) is a possible environmental trigger for AA. METHODS: We queried the National AA Registry for all patients who self-reported sudden onset of AA with concurrent EBV mononucleosis. RESULTS: Among the 6256 individuals registered between December 2001 and August 2007, 1586 patients reported an environmental trigger-including 12 individuals who had an EBV infection within 6 months before the onset of AA. LIMITATIONS: This study relies on self-reported data, and not all medical records confirming EBV infections were available for review. CONCLUSION: The association between EBV and AA is worthy of further investigation.


Subject(s)
Alopecia Areata/epidemiology , Epstein-Barr Virus Infections/epidemiology , Adolescent , Adult , Age of Onset , Alopecia Areata/virology , Causality , Child , Child, Preschool , Comorbidity , Environmental Monitoring/statistics & numerical data , Epidemiological Monitoring , Epstein-Barr Virus Infections/diagnosis , Female , Herpesvirus 4, Human/isolation & purification , Humans , Infectious Mononucleosis/epidemiology , Male , Registries , Retrospective Studies , United States/epidemiology
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