Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 67
Filter
1.
Pediatr Cardiol ; 44(3): 618-623, 2023 Mar.
Article in English | MEDLINE | ID: mdl-35902413

ABSTRACT

The Pediatric Heart Network (PHN) trial showed similar efficacy of ß-blockers (BB) and angiotensin receptor blockers (ARB) for aortic root dilation in Marfan syndrome, but the impact on prescription practices is unknown. We hypothesized BB and ARB prescriptions would increase after the trial results were published (2014). Prescription data (2007-2016) were obtained from outpatient encounters (IBM Marketscan) for Marfan syndrome patients (6 months-25 years old). Excluding 2014 as a washout period, we analyzed two intervals: 2007-2013 and 2015-2016. Medication categories included BB, ARB, angiotensin converting enzyme inhibitors (ACEI), combination (BB/ARB and/or BB/ACEI), and no drug. Interrupted time-series analysis assessed immediate level change after publication and change in slope for the trend pre- and post-publication. Odds ratios (OR) and 95% confidence intervals from logistic regressions and generalized estimating equation methods accounted for correlation of prescriptions within patients. In 1499 patients (age 14.1 ± 6.1 years, 59% female) seen 2007-2013, BB trended lower [OR 0.91 (0.89, 0.93), p < 0.001] and ARB trended higher [OR 1.12 (1.07, 1.18), p < 0.001], while combination, ACEI, and no drug remained stable. This trend persisted, but was not significant, for BB [OR 0.54 (0.27, 1.08), p = 0.37] and ARB [OR 1.91 (0.55, 6.69), p = 0.31] in 2015-2016. Combination, ACEI, and no drug remained similar. In short term follow-up, changes in prescription practices following publication of the PHN trial were not statistically significant. This may be due to a change seen prior to publication with early adoption of ARBs that was maintained after confirmation of their effectiveness.


Subject(s)
Losartan , Marfan Syndrome , Adolescent , Adult , Child , Female , Humans , Male , Young Adult , Adrenergic beta-Antagonists/therapeutic use , Angiotensin II Type 1 Receptor Blockers/therapeutic use , Angiotensin Receptor Antagonists/therapeutic use , Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Atenolol/therapeutic use , Losartan/therapeutic use , Marfan Syndrome/drug therapy , Prescriptions
2.
Am J Cardiol ; 177: 128-136, 2022 08 15.
Article in English | MEDLINE | ID: mdl-35691707

ABSTRACT

Transcatheter aortic valve implantation (TAVI) is common in adults but rare in children and adolescents. Since 2014, our institution has incorporated a transcatheter approach as an option for aortic valve replacement in this population. The purpose of this study was to compare short-term outcomes of TAVI with surgical aortic valve replacement (SAVR). This single-center, retrospective study included patients aged 10 to 21 years who had a native SAVR or TAVI between January 2010 to April 2020. Comparative analysis of baseline characteristics and a composite outcome (stroke within 6 months, readmission within 30 days, death) between SAVR and TAVI were made using chi-square test or Wilcoxon rank sum test, as appropriate. Of the 77 patients who underwent native aortic valve implantation during the study period (60 SAVR, 17 TAVI), 46 were aged 10 to 21 years (30 SAVR, 16 TAVI). Median follow-up was 3.8 years (interquartile range 1.5 to 4.9) for the SAVR group and 1.5 years (interquartile range 1.1 to 1.2) for the TAVI group. There was no difference in the composite outcome between groups. Patients in the SAVR group were more likely to have undergone concomitant surgical intervention and have longer intensive care unit and hospital stays. In conclusion, our study suggests similar short-term outcomes between SAVR and TAVI in children and young adults aged 10 to 21 years. Longer-term studies are essential to understand the utility of TAVI and to better consider the option of a transcatheter approach as an alternative to SAVR in the pediatric population.


Subject(s)
Aortic Valve Stenosis , Heart Defects, Congenital , Heart Valve Prosthesis Implantation , Transcatheter Aortic Valve Replacement , Adolescent , Aortic Valve/surgery , Aortic Valve Stenosis/etiology , Aortic Valve Stenosis/surgery , Child , Heart Defects, Congenital/etiology , Heart Defects, Congenital/surgery , Heart Valve Prosthesis Implantation/adverse effects , Humans , Retrospective Studies , Risk Factors , Transcatheter Aortic Valve Replacement/adverse effects , Treatment Outcome , Young Adult
3.
Neurology ; 2022 May 18.
Article in English | MEDLINE | ID: mdl-35584923

ABSTRACT

Lambl's excrescences are fibrinous connective tissue strands found on predominantly left-sided cardiac valves. These valvular strands are typically benign, but have been implicated as a potential etiology of embolic strokes in adult patients. The significance of Lambl's excrescences in pediatric stroke cases is unclear and not previously reported in the literature. Here, we describe a 10-year-old boy who presented with acute onset right-sided hemiplegia, found to have multifocal embolic strokes of various ages. Extensive stroke workup was unrevealing, aside from the presence of small, filamentous strand-like densities associated with the mitral and aortic valves noted on a transesophageal echocardiogram consistent with Lambl's excrescences. In this case report, we review Lambl's excrescences and their significance in acute stroke, as well as management options for prevention of future ischemia in these patients.

4.
Pediatrics ; 149(3)2022 03 01.
Article in English | MEDLINE | ID: mdl-35229125

ABSTRACT

OBJECTIVES: To characterize the outcomes of ABO incompatible direct antiglobulin test (DAT) positive newborns and determine the predictive ability of a sixth-hour transcutaneous bilirubin (TcB for needing phototherapy ≤24 hours of age. METHODS: Retrospective, cross-sectional study from May 2013 to March 2017. Of 10 942 consecutive newborns ≥35 weeks estimated gestational age, 829 were ABO incompatible and DAT positive. After excluding for antibodies other than ABO (51), missing data (4), miscategorization of blood type O (1), and duplicate record (1), 772 newborns remained. Of 772, a subsample of 346 newborns with both TcB and total serum bilirubin (TSB) tests within 1 hour of the sixth hour was analyzed to determine the predictive ability. RESULTS: Phototherapy was required in 281 of 772 (36.4%); 156 (20.2%) in the first 24 hours. There were 10 (1.3%) admissions for hyperbilirubinemia to the NICU for intravenous immunoglobin. Birth weight, infant blood type B, TSB, reticulocyte count, and TcB were all significantly associated with phototherapy ≤24 hours. On multivariate analysis, significant predictors of phototherapy ≤24 hours were TSB and reticulocyte count if no TcB was done and TcB alone if no blood tests were done. TcB was highly predictive (odds ratio 3.1, 95% confidence interval: 2.4-4.0) and nearly as accurate as the TSB and reticulocyte count (area under the curve, 0.90 and 0.96, respectively). Low (<3.0 mg/dL) and high (≥5.3 mg/dL) risk TcB cutoffs demonstrated a negative predictive value of 98% and positive predictive value of 85%, respectively. CONCLUSIONS: Among high-risk ABO incompatible DAT positive newborns, the sixth-hour TcB is highly predictive of the need for phototherapy ≤24 hours.


Subject(s)
Bilirubin , Jaundice, Neonatal , Cross-Sectional Studies , Humans , Infant , Infant, Newborn , Jaundice, Neonatal/therapy , Neonatal Screening , Phototherapy , Retrospective Studies
5.
Clin Nucl Med ; 45(4): e215-e216, 2020 Apr.
Article in English | MEDLINE | ID: mdl-32049726

ABSTRACT

Three-phase bone scan was performed for evaluation of possible sinus tarsi syndrome in a 52-year-old man with chronic left ankle pain. MRI was initially read as unremarkable, and there was little symptomatic improvement after intra-articular anesthetic injection. The primary finding that appreciated only delayed bone SPECT/CT images was focal increased uptake associated with a well-corticated 8-mm bony fragment adjacent to the left calcaneus, thought to represent an accessory ossicle within the left sinus tarsi. The increased uptake suggested fracture or severe degenerative change of the ossicle, likely contributing to the patient's chronic pain.


Subject(s)
Foot Diseases/diagnostic imaging , Single Photon Emission Computed Tomography Computed Tomography , Tarsal Bones/diagnostic imaging , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Tarsal Bones/pathology
6.
J Card Surg ; 34(10): 1127-1129, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31374579

ABSTRACT

Cardiac myxomas can be fatal and left ventricular (LV) myxomas with papillary muscle and mitral valve (MV) involvement are rare. The following case is that of a 55-year-old woman who developed signs and symptoms of pulmonary hypertension. Imaging revealed a contractile mass in the LV that was in continuum with the papillary muscles and affected MV function. Her clinical course, radiologic, and hemodynamic findings are discussed. Finally, her surgical extraction technique is described in addition to potential complications encountered.


Subject(s)
Heart Neoplasms/diagnosis , Hypertension, Pulmonary/etiology , Myxoma/diagnosis , Echocardiography , Female , Heart Neoplasms/complications , Heart Neoplasms/surgery , Heart Ventricles , Humans , Hypertension, Pulmonary/diagnosis , Hypertension, Pulmonary/surgery , Magnetic Resonance Imaging, Cine , Middle Aged , Mitral Valve , Myxoma/complications , Myxoma/surgery , Papillary Muscles , Positron-Emission Tomography , Severity of Illness Index , Tomography, X-Ray Computed
7.
J Clin Invest ; 129(7): 2745-2759, 2019 05 14.
Article in English | MEDLINE | ID: mdl-31085833

ABSTRACT

Mobilized peripheral blood has become the primary source of hematopoietic stem and progenitor cells (HSPCs) for stem cell transplantation, with a five-day course of granulocyte colony stimulating factor (G-CSF) as the most common regimen used for HSPC mobilization. The CXCR4 inhibitor, plerixafor, is a more rapid mobilizer, yet not potent enough when used as a single agent, thus emphasizing the need for faster acting agents with more predictable mobilization responses and fewer side effects. We sought to improve hematopoietic stem cell transplantation by developing a new mobilization strategy in mice through combined targeting of the chemokine receptor CXCR2 and the very late antigen 4 (VLA4) integrin. Rapid and synergistic mobilization of HSPCs along with an enhanced recruitment of true HSCs was achieved when a CXCR2 agonist was co-administered in conjunction with a VLA4 inhibitor. Mechanistic studies revealed involvement of CXCR2 expressed on BM stroma in addition to stimulation of the receptor on granulocytes in the regulation of HSPC localization and egress. Given the rapid kinetics and potency of HSPC mobilization provided by the VLA4 inhibitor and CXCR2 agonist combination in mice compared to currently approved HSPC mobilization methods, it represents an exciting potential strategy for clinical development in the future.


Subject(s)
Bone Marrow/metabolism , Hematopoietic Stem Cell Mobilization , Hematopoietic Stem Cell Transplantation , Hematopoietic Stem Cells/metabolism , Integrin alpha4beta1 , Receptors, Interleukin-8B , Allografts , Animals , Granulocytes/metabolism , Integrin alpha4beta1/antagonists & inhibitors , Integrin alpha4beta1/genetics , Integrin alpha4beta1/metabolism , Mice , Mice, Inbred BALB C , Mice, Knockout , Receptors, Interleukin-8B/antagonists & inhibitors , Receptors, Interleukin-8B/genetics , Receptors, Interleukin-8B/metabolism
8.
Matrix Biol ; 82: 86-104, 2019 09.
Article in English | MEDLINE | ID: mdl-31004743

ABSTRACT

The extracellular matrix (ECM) microenvironment is increasingly implicated in the instruction of pathologically relevant cell behaviors, from aberrant transdifferentation to invasion and beyond. Indeed, pathologic ECMs possess a panoply of alterations that provide deleterious instructions to resident cells. Here we demonstrate the precise manner in which the ECM protein fibronectin (FN) undergoes the posttranslational modification citrullination in response to peptidyl-arginine deiminase (PAD), an enzyme associated with innate immune cell activity and implicated in systemic ECM-centric diseases, like cancer, fibrosis and rheumatoid arthritis. FN can be citrullinated in at least 24 locations, 5 of which reside in FN's primary cell-binding domain. Citrullination of FN alters integrin clustering and focal adhesion stability with a concomitant enhancement in force-triggered integrin signaling along the FAK-Src and ILK-Parvin pathways within fibroblasts. In vitro migration and in vivo wound healing studies demonstrate the ability of citrullinated FN to support a more migratory/invasive phenotype that enables more rapid wound closure. These findings highlight the potential of ECM, particularly FN, to "record" inflammatory insults via post-translational modification by inflammation-associated enzymes that are subsequently "read" by resident tissue fibroblasts, establishing a direct link between inflammation and tissue homeostasis and pathogenesis through the matrix.


Subject(s)
Fibronectins/metabolism , Focal Adhesions/metabolism , Integrins/metabolism , Stromal Cells/cytology , Animals , Binding Sites , Cell Adhesion , Cell Movement , Cells, Cultured , Citrullination , Extracellular Matrix/metabolism , Female , Fibronectins/chemistry , Humans , Male , Mice , Protein-Arginine Deiminases/metabolism , Signal Transduction , Stromal Cells/metabolism
10.
Crit Care Explor ; 1(8): e0036, 2019 Aug.
Article in English | MEDLINE | ID: mdl-32166277

ABSTRACT

Severe sepsis and septic shock continue to be an important problem in children, with hospital mortality rates for pediatric severe sepsis as high as 25%. CASE SUMMARY: Two pediatric patients with septic shock requiring high dose vasopressors, who were treated with angiotensin II as part of an open-label study. Both patients had a significant increase in mean arterial pressure shortly after initiation of angiotensin II, with a reduction of the dose of catecholamines and vasopressin infusions. Serious adverse events reported were not attributable to angiotensin II by investigators. One patient survived, and one died related to progressive cerebral edema. CONCLUSIONS: Angiotensin II may represent another therapeutic option for pediatric patients who remain hypotensive despite receiving fluids and standard vasopressor therapy and deserves further study.

12.
J Biol Chem ; 293(41): 15867-15886, 2018 10 12.
Article in English | MEDLINE | ID: mdl-30108174

ABSTRACT

Transforming growth factor-ß (TGFß) signaling through SMAD2/3 is an important driver of pathological fibrosis in multiple organ systems. TGFß signaling and extracellular matrix (ECM) stiffness form an unvirtuous pathological circuit in which matrix stiffness drives activation of latent TGFß, and TGFß signaling then drives cellular stress and ECM synthesis. Moreover, ECM stiffness also appears to sensitize cells to exogenously activated TGFß through unknown mechanisms. Here, using human fibroblasts, we explored the effect of ECM stiffness on a putative inner nuclear membrane protein, LEM domain-containing protein 3 (LEMD3), which is physically connected to the cell's actin cytoskeleton and inhibits TGFß signaling. We showed that LEMD3-SMAD2/3 interactions are inversely correlated with ECM stiffness and TGFß-driven luciferase activity and that LEMD3 expression is correlated with the mechanical response of the TGFß-driven luciferase reporter. We found that actin polymerization but not cellular stress or LEMD3-nuclear-cytoplasmic couplings were necessary for LEMD3-SMAD2/3 interactions. Intriguingly, LEMD3 and SMAD2/3 frequently interacted in the cytosol, and we discovered LEMD3 was proteolytically cleaved into protein fragments. We confirmed that a consensus C-terminal LEMD3 fragment binds SMAD2/3 in a stiffness-dependent manner throughout the cell and is sufficient for antagonizing SMAD2/3 signaling. Using human lung biopsies, we observed that these nuclear and cytosolic interactions are also present in tissue and found that fibrotic tissues exhibit locally diminished and cytoplasmically shifted LEMD3-SMAD2/3 interactions, as noted in vitro Our work reveals novel LEMD3 biology and stiffness-dependent regulation of TGFß by LEMD3, providing a novel target to antagonize pathological TGFß signaling.


Subject(s)
Mechanotransduction, Cellular/drug effects , Membrane Proteins/metabolism , Nuclear Proteins/metabolism , Smad2 Protein/metabolism , Smad3 Protein/metabolism , Transforming Growth Factor beta/metabolism , Actins/metabolism , Cytosol/metabolism , DNA-Binding Proteins , Extracellular Matrix/metabolism , Fibroblasts/metabolism , Humans , Idiopathic Pulmonary Fibrosis/metabolism , Lung/metabolism , Membrane Proteins/antagonists & inhibitors , Membrane Proteins/chemistry , Nuclear Lamina/metabolism , Nuclear Proteins/antagonists & inhibitors , Nuclear Proteins/chemistry , Peptide Fragments/chemistry , Peptide Fragments/metabolism , Phosphorylation , Protein Phosphatase 2C/metabolism , Smad2 Protein/antagonists & inhibitors , Smad2 Protein/chemistry , Smad3 Protein/antagonists & inhibitors , Smad3 Protein/chemistry , Transforming Growth Factor beta/antagonists & inhibitors
13.
Clin Transl Sci ; 11(4): 412-419, 2018 07.
Article in English | MEDLINE | ID: mdl-29603633

ABSTRACT

Advances in therapies have led to prolonged survival from many previously lethal health threats in children, notably among prematurely born babies and those with congenital heart disease. Evidence for catch-up growth is common in these children, but in many cases the adult phenotype is never achieved. A translational animal model is required in which specific tissues can be studied over a reasonable time interval. We investigated the impact of postnatal hypoxia (HY) (12%O2 (HY12) or 10% O2 (HY10)) on growth in rats relative to animals raised in room air. Subgroups had access to running wheels following the HY period. Growth was fully compensated in adult HY12 rats but not HY10 rats. The results of this study indicate that neonatal hypoxia can be a useful model for the elucidation of mechanisms that mediate successful catch-up growth following neonatal insults and identify the critical factors that prevent successful catch-up growth.


Subject(s)
Disease Models, Animal , Growth/physiology , Hypoxia/physiopathology , Premature Birth/physiopathology , Animals , Animals, Newborn , Body Height/physiology , Body Weight/physiology , Female , Humans , Hypoxia/pathology , Infant , Infant, Newborn , Male , Pregnancy , Premature Birth/pathology , Random Allocation , Rats , Rats, Sprague-Dawley
14.
Cell ; 172(1-2): 191-204.e10, 2018 01 11.
Article in English | MEDLINE | ID: mdl-29224778

ABSTRACT

Hematopoietic stem cell transplantation is a potential curative therapy for malignant and nonmalignant diseases. Improving the efficiency of stem cell collection and the quality of the cells acquired can broaden the donor pool and improve patient outcomes. We developed a rapid stem cell mobilization regimen utilizing a unique CXCR2 agonist, GROß, and the CXCR4 antagonist AMD3100. A single injection of both agents resulted in stem cell mobilization peaking within 15 min that was equivalent in magnitude to a standard multi-day regimen of granulocyte colony-stimulating factor (G-CSF). Mechanistic studies determined that rapid mobilization results from synergistic signaling on neutrophils, resulting in enhanced MMP-9 release, and unexpectedly revealed genetic polymorphisms in MMP-9 that alter activity. This mobilization regimen results in preferential trafficking of stem cells that demonstrate a higher engraftment efficiency than those mobilized by G-CSF. Our studies suggest a potential new strategy for the rapid collection of an improved hematopoietic graft.


Subject(s)
Hematopoietic Stem Cell Mobilization/methods , Hematopoietic Stem Cell Transplantation/methods , Hematopoietic Stem Cells/immunology , Adult , Animals , Benzylamines , Chemokine CXCL2/pharmacology , Cyclams , Female , Hematopoietic Stem Cells/drug effects , Heterocyclic Compounds/pharmacology , Humans , Male , Matrix Metalloproteinase 9/genetics , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Inbred DBA , Mice, Inbred ICR , Polymorphism, Genetic
15.
Clin Nucl Med ; 43(1): e27-e28, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29189376

ABSTRACT

I-NaI thyroid uptake and scan in a 46-year-old woman with symptomatic hyperthyroidism demonstrated marked, diffusely increased uptake consistent with Graves disease, as well as a solitary hypofunctioning ("cold") nodule. Pathologic evaluation following total thyroidectomy and selective neck dissection revealed invasive multifocal papillary thyroid carcinoma in a background of Graves disease and 5 of 36 lymph nodes positive for metastatic disease. This case serves as a reminder that when present a cold nodule in the setting of Graves disease warrants further evaluation for underlying malignancy.


Subject(s)
Graves Disease/complications , Thyroid Nodule/complications , Female , Humans , Middle Aged , Neoplasm Metastasis , Radionuclide Imaging , Thyroid Nodule/diagnostic imaging , Thyroid Nodule/pathology , Thyroid Nodule/surgery
16.
Clin Nucl Med ; 42(1): 73-75, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27824318

ABSTRACT

A 45-year-old man underwent FDG PET/CT for initial imaging evaluation of recurrent Escherichia coli urinary tract infections, which demonstrated no significant FDG uptake in either kidney and subtle FDG uptake in the right prostate lobe. Subsequent Ga SPECT/CT demonstrated abnormal intense gallium uptake throughout the right kidney and entire prostate gland, clearly discordant with PET/CT findings and consistent with unexpected concurrent pyelonephritis and prostatitis. Although FDG has effectively replaced Ga in everyday clinical practice, the current case serves as a reminder that there is still a role for Ga in the evaluation of genitourinary infections.


Subject(s)
Escherichia coli Infections/diagnostic imaging , Prostatitis/diagnostic imaging , Pyelonephritis/diagnostic imaging , Urinary Tract Infections/diagnostic imaging , Escherichia coli Infections/complications , Fluorodeoxyglucose F18 , Gallium Radioisotopes , Humans , Male , Middle Aged , Positron Emission Tomography Computed Tomography , Prostatitis/complications , Pyelonephritis/complications , Radiopharmaceuticals , Single Photon Emission Computed Tomography Computed Tomography , Urinary Tract Infections/complications
17.
J Environ Sci Health B ; 51(9): 654, 2016 09.
Article in English | MEDLINE | ID: mdl-27337288
18.
J Environ Sci Health B ; 51(6): 366-73, 2016.
Article in English | MEDLINE | ID: mdl-26950528

ABSTRACT

We employed our inhalation methodology to examine whether biomarkers of inflammation and oxidative stress would be produced in mice following inhalation of aerosols containing carbonaceous particles or the vapor of pesticides prevalent during the first Gulf War. Exposure to two putative Gulf War Illness toxins, fine airborne particles and the pesticide malathion, increased biomarkers of inflammation and oxidative stress in Friend virus B (FVB) female mice. Mice inhaling particles 24 h before had increased lung lavage and plasma Leukotriene B4 (LTB4) (a biomarker of inflammation) and PGF2α (a biomarker of oxidative stress) levels, lung lavage protein and lung lavage lactic dehydrogenase (LDH) levels. These changes were a function of particle density and exposure time. Compared to particle inhalation, mice inhaling malathion 24 h before had small increase in plasma LTB4 and PGF2α levels but no increase in lung lavage LTB4, lung lavage protein, lung lavage LDH, and lung lavage alveolar macrophage (AM) levels compared to unexposed control mice. AM from particle-exposed mice contained phagocytosed particles, while AM from malathion-exposed mice showed no abnormalities. Our results indicate that inhaling particles or malathion can alter inflammatory and oxidative biomarkers in mice and raise the possibility that these toxins may have altered inflammation and oxidative stress biomarkers in Gulf War-exposed individuals.


Subject(s)
Aerosols/toxicity , Malathion/toxicity , Oxidative Stress/drug effects , Administration, Inhalation , Aerosols/administration & dosage , Animals , Biomarkers/analysis , Biomarkers/metabolism , Bronchoalveolar Lavage Fluid , Dinoprost/analysis , Dinoprost/metabolism , Environmental Exposure/adverse effects , Female , Gulf War , Inflammation/chemically induced , Inflammation/metabolism , Leukotriene B4/analysis , Leukotriene B4/metabolism , Macrophages, Alveolar/drug effects , Malathion/administration & dosage , Mice , Mice, Inbred Strains , Particle Size
19.
Clin Nucl Med ; 41(6): e301-3, 2016 Jun.
Article in English | MEDLINE | ID: mdl-26825200

ABSTRACT

Brain MRI in an 82-year-old man with presumed Bell's palsy revealed a clinically unsuspected right parotid gland mass but no other acute findings. Biopsy revealed poorly differentiated adenocarcinoma. Staging F-FDG PET/CT revealed an FDG-avid parotid mass, abnormal FDG uptake along the course of the facial nerve from mass to skull base, and multiple FDG-avid right level II neck lymph nodes and hepatic metastases. The PET/CT findings and prolonged clinical course suggest that diffuse perineural spread of tumor from a smoldering parotid neoplasm, and not idiopathic Bell's palsy, was responsible for the patient's facial paralysis.


Subject(s)
Adenocarcinoma/pathology , Facial Paralysis/complications , Facial Paralysis/diagnostic imaging , Nervous System Neoplasms/complications , Nervous System Neoplasms/secondary , Parotid Neoplasms/pathology , Positron Emission Tomography Computed Tomography , Aged, 80 and over , Humans , Male , Parotid Gland/innervation
20.
Bioorg Med Chem Lett ; 23(17): 4979-84, 2013 Sep 01.
Article in English | MEDLINE | ID: mdl-23886683

ABSTRACT

Lead optimization of piperidine amide HTS hits, based on an anilino-thiazole core, led to the identification of analogs which displayed low nanomolar blocking activity at the canonical transient receptor channels 3 and 6 (TRPC3 & 6) based on FLIPR (carbachol stimulated) and electrophysiology (OAG stimulated) assays. In addition, the anilino-thiazole amides displayed good selectivity over other TRP channels (TRPA1, TRPV1, and TRPV4), as well as against cardiac ion channels (CaV1.2, hERG, and NaV1.5). The high oxidation potential of the aliphatic piperidine and aniline groups, as well as the lability of the thiazole amide group contributed to the high clearance observed for this class of compounds. Conversion of an isoquinoline amide to a naphthyridine amide markedly reduced clearance for the bicyclic piperidines, and improved oral bioavailability for this compound series, however TRPC3 and TRPC6 blocking activity was reduced substantially. Although the most potent anilino-thiazole amides ultimately lacked oral exposure in rodents and were not suitable for chronic dosing, analogs such as 14-19, 22, and 23 are potentially valuable in vitro tool compounds for investigating the role of TRPC3 and TRPC6 in cardiovascular disease.


Subject(s)
Aniline Compounds/chemistry , Aniline Compounds/pharmacology , TRPC Cation Channels/antagonists & inhibitors , Thiazoles/chemistry , Thiazoles/pharmacology , Diglycerides/metabolism , Drug Discovery , HEK293 Cells , Humans , TRPC Cation Channels/metabolism , TRPC6 Cation Channel
SELECTION OF CITATIONS
SEARCH DETAIL
...