keyword
https://read.qxmd.com/read/38695646/ionic-liquid-gating-induces-anomalous-permeation-through-membrane-channel-proteins
#1
JOURNAL ARTICLE
Ju Liu, Yanlei Wang, Bo Gao, Kun Zhang, Hui Li, Jing Ren, Feng Huo, Baofeng Zhao, Lihua Zhang, Suojiang Zhang, Hongyan He
Membrane channel proteins (MCPs) play key roles in matter transport through cell membranes and act as major targets for vaccines and drugs. For emerging ionic liquid (IL) drugs, a rational understanding of how ILs affect the structure and transport function of MCP is crucial to their design. In this work, GPU-accelerated microsecond-long molecular dynamics simulations were employed to investigate the modulating mechanism of ILs on MCP. Interestingly, ILs prefer to insert into the lipid bilayer and channel of aquaporin-2 (AQP2 ) but adsorb on the entrance of voltage-gated sodium channels (Nav)...
May 2, 2024: Journal of the American Chemical Society
https://read.qxmd.com/read/38695074/kidney-collecting-duct-derived-vasopressin-is-not-essential-for-appropriate-concentration-or-dilution-of-urine
#2
JOURNAL ARTICLE
Yvonne Zuchowski, Joshua Carty, Jonathan B Trapani, Jason Watts, Fabian Bock, Mingzhi Zhang, Andrew Terker, Roy Zent, Eric Delpire, Raymond C Harris, Juan Pablo Arroyo
We previously showed that kidney collecting ducts make vasopressin. However, the physiologic role of collecting-duct-derived vasopressin is uncertain. We hypothesized that collecting-duct-derived vasopressin was required for appropriate concentration of urine. We developed a vasopressin conditional knockout mouse model wherein Cre recombinase expression induces deletion of Avp exon 1 in the distal nephron. We then used age-matched 8 - 12 week old Avp fl/fl; Ksp -Cre(-) (WT) and Avp fl/fl; Ksp -Cre(+) mice for all experiments...
May 2, 2024: American Journal of Physiology. Renal Physiology
https://read.qxmd.com/read/38693608/concurrent-retinal-vasculitis-and-optic-neuritis-in-aquaporin-4-positive-neuromyelitis-optica-spectrum-disorder-a-case-report
#3
JOURNAL ARTICLE
Wenjun Song, Graham E Holder, Rupesh Agrawal, Melissa C H Tien
No abstract text is available yet for this article.
May 2, 2024: Journal of Neuro-ophthalmology: the Official Journal of the North American Neuro-Ophthalmology Society
https://read.qxmd.com/read/38692159/the-relation-between-autophagy-modulation-by-intermittent-fasting-and-aquaporin-2-expression-in-experimentally-induced-diabetic-nephropathy-in-albino-rat
#4
JOURNAL ARTICLE
Nora Hisham Hassan, Dalia Saleh, Salwa M Abo El-Khair, Shaima M Almasry, Amira Ibrahim
Polyuria is an early sign of diabetic nephropathy (DN) that produces dehydration in diabetic patients. This could be caused by alteration of renal aquaporin 2 (AQP2) expression. This study aimed to describe the relation between autophagy modulation via intermittent fasting (IF) and renal AQP2 expression and polyuria in case of DN. We divided the rats into control, DN and IF groups. After 2 and 4 weeks of diabetes induction, blood glucose (BG), serum creatinine (Scr), urine volume, and 24 hours urine protein (UP) were examined...
April 22, 2024: Tissue & Cell
https://read.qxmd.com/read/38689876/case-report-transition-from-anti-cd20-therapy-to-inebilizumab-for-14-cases-of-neuromyelitis-optica-spectrum-disorder
#5
Benjamin Osborne, Gabriela Romanow, J Michael Hemphill, Myassar Zarif, Tracy DeAngelis, Tyler Kaplan, Unsong Oh, Johnathan Pinkhasov, Kristina Patterson, Michael Levy
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disorder of the central nervous system characterized by recurrent, disabling attacks that affect the optic nerve, spinal cord, and brain/brainstem. While rituximab, targeting CD20-positive B-cells, is used as an off-label therapy for NMOSD, some patients continue to exhibit breakthrough attacks and/or adverse reactions. Inebilizumab, a humanized and glycoengineered monoclonal antibody targeting CD19-positive B-cells, has been FDA approved for the treatment of NMOSD in adult patients who are anti-aquaporin-4 (AQP4) antibody positive...
2024: Frontiers in Neurology
https://read.qxmd.com/read/38688829/impacts-of-age-and-gender-on-brain-edema-in-a-mouse-water-intoxication-model
#6
JOURNAL ARTICLE
Emi Nakamura-Maruyama, Keiichiro Irie, Kazuhiko Narita, Naoyuki Himi, Osamu Miyamoto, Takehiro Nakamura
Brain edema causes abnormal fluid retention and can be fatal in severe cases. Although it develops in various diseases, most treatments for brain edema are classical. We analyzed the impacts of age and gender on the characteristics of a water intoxication model that induces pure brain edema in mice and examined the model's usefulness for research regarding new treatments for brain edema. C57BL/6J mice received an intraperitoneal administration of 10% body weight distilled water, and we calculated the brain water content by measuring the brain-tissue weight immediately after dissection and after drying...
April 2024: Acta Medica Okayama
https://read.qxmd.com/read/38688399/transcranial-direct-current-stimulation-alters-cerebrospinal-fluid-interstitial-fluid-exchange-in-mouse-brain
#7
JOURNAL ARTICLE
Yan Wan, Hiromu Monai
BACKGROUND: Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that has gained prominence recently. Clinical studies have explored tDCS as an adjunct to neurologic disease rehabilitation, with evidence suggesting its potential in modulating brain clearance mechanisms. The glymphatic system, a proposed brain waste clearance system, posits that cerebrospinal fluid-interstitial fluid (CSF-ISF) exchange aids in efficient metabolic waste removal. While some studies have linked tDCS to astrocytes inositol trisphosphate (IP3 )/Ca2+ signaling, the impact of tDCS on CSF-ISF exchange dynamics remains unclear...
April 28, 2024: Brain Stimulation
https://read.qxmd.com/read/38687723/identification-of-core-genes-involved-in-the-response-of-apocynum-venetum-to-salt-stress-based-on-transcriptome-sequencing-and-wgcna
#8
JOURNAL ARTICLE
Xi Zhen, Xuyang Liu, Xiaoming Zhang, Shujie Luo, Wencheng Wang, Tao Wan
Apocynum venetum L. belongs to the Apocynaceae family and is a plant that is highly resistant to stress. It is important in the fields of ecology, feeding, industry and medicine. The molecular mechanism underlying salt tolerance has not been elucidated. In this study, RNA-seq based transcriptome sequencing of A. venetum leaves after 0, 2, 6, 12, 24 and 48 h of treatment with 300 mM NaCl was performed. We conducted a comprehensive analysis of the transcriptome expression profiles of A. venetum under salt stress using the WGCNA method and identified red, black, and brown as the core modules regulating the salt tolerance of A...
2024: PloS One
https://read.qxmd.com/read/38687396/correction-to-connexin-43-promotes-neurogenesis-via-regulating-aquaporin-4-after-cerebral-ischemia
#9
Heling Chu, Jing Dong, Yuping Tang, Chuyi Huang, Qihao Guo
No abstract text is available yet for this article.
April 30, 2024: Neurotoxicity Research
https://read.qxmd.com/read/38683409/from-swamp-to-field-how-genes-from-mangroves-and-its-associates-can-enhance-crop-salinity-tolerance
#10
REVIEW
Ganesan Govindan, Prakash Harini, Vinoth Alphonse, Madasamy Parani
Salinity stress is a critical challenge in crop production and requires innovative strategies to enhance the salt tolerance of plants. Insights from mangrove species, which are renowned for their adaptability to high-salinity environments, provides valuable genetic targets and resources for improving crops. A significant hurdle in salinity stress is the excessive uptake of sodium ions (Na+ ) by plant roots, causing disruptions in cellular balance, nutrient deficiencies, and hampered growth. Specific ion transporters and channels play crucial roles in maintaining a low Na+ /K+ ratio in root cells which is pivotal for salt tolerance...
April 29, 2024: Molecular Biology Reports
https://read.qxmd.com/read/38683074/-in-silico-analysis-of-molecular-mimicry-between-human-aquaporin-3-aspergillus-fumigatus-aquaporin-and-aquaporins-from-allergic-sources
#11
JOURNAL ARTICLE
Andrés Sánchez, Yaquelin Padilla, Adriana Lorduy, Jorge Sánchez, Marlon Múnera, Claudia Baena, Carlos Bernal, Juan Urrego
OBJECTIVE: Conduct an in-silico assessment of potential molecular mimicry between human aquaporins, A. fumigatus , and diverse allergenic sources. METHODS: Amino acid sequences of human AQP3 and A. fumigatus aquaporin were compared through multiple alignments with 25 aquaporins from diverse allergenic sources. Phylogenetic analysis and homology-based modeling were executed, and the ElliPro server predicted conserved antigenic regions on 3D structures. RESULTS: Global identity among studied aquaporins was 32...
February 1, 2024: Revista Alergia Mexico: Organo Oficial de la Sociedad Mexicana de Alergia e Inmunología, A.C
https://read.qxmd.com/read/38682293/single-molecule-imaging-of-aquaporin-4-array-dynamics-in-astrocytes
#12
JOURNAL ARTICLE
Anna-Lena Zepernick, Vanya Metodieva, Noelia Pelegrina-Hidalgo, Anna H Lippert, Mathew H Horrocks, Juan A Varela
Aquaporin-4 (AQP4) facilitates water transport across astrocytic membranes in the brain, forming highly structured nanometric arrays. AQP4 has a central role in regulating cerebrospinal fluid (CSF) circulation and facilitating the clearance of solutes from the extracellular space of the brain. Adrenergic signaling has been shown to modulate the volume of the extracellular space of the brain via AQP4 localized at the end-feet of astrocytes, but the mechanisms by which AQP4 regulates CSF inflow and outflow in the brain remain elusive...
April 29, 2024: Nanoscale
https://read.qxmd.com/read/38682226/neuromyelitis-optica-spectrum-disorder-in-latin-america-state-of-the-art-and-current-challenges
#13
REVIEW
Edgar Carnero Contentti, Bárbara Eizaguirre, Pablo A López, Berenice Silva, Verónica A Tkachuk, Santiago Tizio, Ricardo Alonso
Neuromyelitis optica spectrum disorder (NMOSD) is a rare autoimmune disease of the central nervous system characterized by severe attacks of optic neuritis, myelitis, and/or area postrema. Advances in understanding the pathophysiology of NMOSD have led to improved diagnostic and therapeutic approaches. There has been a notable increase in research efforts worldwide, including in Latin America (LATAM). In recent years, LATAM has witnessed a surge in research on NMOSD, resulting in a growing body of evidence on various aspects such as epidemiology, clinical manifestations, paraclinical features (including AQP4-IgG [Aquaporin-4-immunoglobulin G] and imaging), acute and long-term treatment strategies, as well as accessibility to diagnostic tests...
April 7, 2024: Journal of Integrative Neuroscience
https://read.qxmd.com/read/38681400/double-seronegative-neuromyelitis-optica-spectrum-disorder-with-longitudinally-extensive-transverse-myelitis-and-optic-neuritis-a-challenging-case-report
#14
Goh Chon Han, Tajunisah Iqbal, Gowri Supramaniam
Neuromyelitis optica spectrum disorder (NMOSD) is a rare antibody-mediated neuroinflammatory disease of the central nervous system, typically manifesting in the optic nerves, spinal cord, and other regions of the central nervous system. We hereby report a case of a 16-year-old girl who presented with a six-month history of transverse myelitis with an acute episode of bilateral retrobulbar optic neuritis. MRI revealed patchy contrast enhancements over bilateral retrobulbar intraorbital optic nerves together with long-segment spinal cord hyperintensities (C2 to T2 level)...
March 2024: Curēus
https://read.qxmd.com/read/38677537/lung-fibroblast-derived-extracellular-vesicles-and-soluble-factors-alleviate-elastase-induced-lung-injury
#15
JOURNAL ARTICLE
Luke van der Koog, Myrthe J Boerrigter, Iris C Gorter, Reinoud Gosens, Anika Nagelkerke
One of the main pathological features of chronic obstructive pulmonary disease (COPD) is the loss of functional alveolar tissue as a consequence of impaired regenerative capacities (emphysema). Recent research suggests that the secretome from mesenchymal cells, particularly extracellular vesicles (EVs), may possess regenerative properties beneficial for lung repair. However, the regenerative potential of the soluble factors (SFs) within the secretome remains largely unexplored in COPD. To this extent, we purified EVs and SFs secreted by lung fibroblasts to generate EV-enriched and SF-enriched fractions, and evaluated their effects on elastase-induced lung injury in both precision-cut lung slices (PCLS) and a mouse model...
April 25, 2024: European Journal of Pharmacology
https://read.qxmd.com/read/38673792/aquaporin-zmtip2-3-promotes-drought-resistance-of-maize-through-symbiosis-with-arbuscular-mycorrhizal-fungi
#16
JOURNAL ARTICLE
Deyin Wang, Ying Ni, Kailing Xie, Yuanhao Li, Wenxiang Wu, Hanchen Shan, Beijiu Cheng, Xiaoyu Li
Arbuscular mycorrhizal fungi symbiosis plays important roles in enhancing plant tolerance to biotic and abiotic stresses. Aquaporins have also been linked to improved drought tolerance in plants and the regulation of water transport. However, the mechanisms that underlie this association remain to be further explored. In this study, we found that arbuscular mycorrhiza fungi symbiosis could induce the gene expression of the aquaporin ZmTIP2;3 in maize roots. Moreover, compared with the wild-type plants, the maize zmtip2;3 mutant also showed a lower total biomass, colonization rate, relative water content, and POD and SOD activities after arbuscular mycorrhiza fungi symbiosis under drought stress...
April 10, 2024: International Journal of Molecular Sciences
https://read.qxmd.com/read/38671467/blood-brain-barrier-permeability-and-astrocyte-derived-extracellular-vesicles-in-children-with-juvenile-idiopathic-arthritis-a-cross-sectional-study
#17
JOURNAL ARTICLE
Lillemor Berntson, Andreas Elfving, Alice Gabrielsson Samuelsson, Anders Öman, Fariborz Mobarrez
BACKGROUND: Juvenile idiopathic arthritis (JIA) is the most prevalent rheumatic disease in children, and the inflammatory process is widely studied, primarily characterized by its impact on joint health. Emerging evidence suggests that JIA may also affect the central nervous system (CNS). This study investigates the potential CNS involvement in JIA by analyzing the presence of astrocyte-derived extracellular vesicles (EVs) and the S100B protein in plasma, both of which are indicative of astrocyte activity and blood-brain barrier (BBB) integrity...
April 26, 2024: Pediatric Rheumatology Online Journal
https://read.qxmd.com/read/38668786/mechanistic-complement-of-autosomal-dominant-polycystic-kidney-disease-the-role-of-aquaporins
#18
REVIEW
Qiumei Lan, Jie Li, Hanqing Zhang, Zijun Zhou, Yaxuan Fang, Bo Yang
Autosomal dominant polycystic kidney disease is a genetic kidney disease caused by mutations in the genes PKD1 or PKD2. Its course is characterized by the formation of progressively enlarged cysts in the renal tubules bilaterally. The basic genetic explanation for autosomal dominant polycystic kidney disease is the double-hit theory, and many of its mechanistic issues can be explained by the cilia doctrine. However, the precise molecular mechanisms underpinning this condition's occurrence are still not completely understood...
April 26, 2024: Journal of Molecular Medicine: Official Organ of the "Gesellschaft Deutscher Naturforscher und Ärzte"
https://read.qxmd.com/read/38667332/aav-mediated-restoration-of-dystrophin-dp71-in-the-brain-of-dp71-null-mice-molecular-cellular-and-behavioral-outcomes
#19
JOURNAL ARTICLE
Ophélie Vacca, Faouzi Zarrouki, Charlotte Izabelle, Mehdi Belmaati Cherkaoui, Alvaro Rendon, Deniz Dalkara, Cyrille Vaillend
A deficiency in the shortest dystrophin-gene product, Dp71, is a pivotal aggravating factor for intellectual disabilities in Duchenne muscular dystrophy (DMD). Recent advances in preclinical research have achieved some success in compensating both muscle and brain dysfunctions associated with DMD, notably using exon skipping strategies. However, this has not been studied for distal mutations in the DMD gene leading to Dp71 loss. In this study, we aimed to restore brain Dp71 expression in the Dp71-null transgenic mouse using an adeno-associated virus (AAV) administrated either by intracardiac injections at P4 (ICP4) or by bilateral intracerebroventricular (ICV) injections in adults...
April 20, 2024: Cells
https://read.qxmd.com/read/38666289/neuromyelitis-optica-spectrum-disorder-resembling-wernicke-s-encephalopathy-a-case-report-and-review-of-the-literature
#20
Sloan Lynch, Nil Saez Calveras, Anik Amin
We describe a case of Neuromyelitis Optica Spectrum Disorder (NMOSD) mimicking Wernicke's Encephalopathy (WE) to highlight an atypical presentation of NMOSD. A 39-year-old female presented with subacute encephalopathy and progressive ophthalmoplegia. Her MRI revealed T2 hyperintensities involving the mammillary bodies, periaqueductal grey matter, medial thalami, third ventricle, and area postrema. Whole blood thiamine levels were elevated and she did not improve with IV thiamine. CSF was notable for lymphocytic pleocytosis and elevated protein...
April 2024: Neurohospitalist
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