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1.
Fitoterapia ; 172: 105744, 2024 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-37952762

RESUMEN

PURPOSE: Frankincense has been shown in studies to have healing benefits for people with ulcerative colitis (UC). However, its underlying mechanisms have not been fully investigated. The objective of this study was to explore the potential molecular mechanisms of Frankincense essential oil (FREO) in improving dextran sodium sulfate (DSS)-induced UC from multiple perspectives. METHODS: The FREO components were analyzed by GC-MS, and the interactions between the key active components and the mechanism of FREO were determined based on RNA-seq, "quantity-effect" weighting coefficient network pharmacology, WGCNA and pharmacodynamic experiments. The protection of FREO against DSS-induced UC mice was assessed by behavioral and pathological changes through mice. The expression of pro-inflammatory cytokines was measured using enzyme-linked immunosorbent assay. The expression of MAPK and NF-κB-related proteins by the Western Blotting and immunohistochemistry method. RESULTS: Treatment with FREO significantly improved the symptoms of weight loss, diarrhea, stool blood, and colon shortening in UC mice. Reduced intestinal mucosal damage and the degree of inflammatory cell infiltration in the colon. Decreased TNF-α and IL-6 levels in mice's serum and inhibited phosphorylation of ERK, p65 in MAPK and NF-κB signaling. CONCLUSION: FREO may decrease the inflammatory response to reduce the symptoms of UC by modulating the MAPK/ NF-κB pathway. This may be due to the synergistic interaction of the effective ingredient Hepten-2-yl tiglate, 6-methyl-5-, Isoneocembrene A and P-Cymene. This study provides a promising drug candidate and a new concept for the treatment of UC.


Asunto(s)
Colitis Ulcerosa , Colitis , Olíbano , Aceites Volátiles , Sulfatos , Humanos , Animales , Ratones , Colitis Ulcerosa/inducido químicamente , Colitis Ulcerosa/tratamiento farmacológico , Colitis Ulcerosa/patología , FN-kappa B/metabolismo , Dextranos/metabolismo , Dextranos/farmacología , Dextranos/uso terapéutico , Olíbano/metabolismo , Olíbano/farmacología , Olíbano/uso terapéutico , Aceites Volátiles/farmacología , RNA-Seq , Modelos Animales de Enfermedad , Estructura Molecular , Sulfato de Dextran/efectos adversos , Sulfato de Dextran/metabolismo , Colon/metabolismo , Colon/patología , Ratones Endogámicos C57BL , Colitis/tratamiento farmacológico
2.
Nutrients ; 15(12)2023 Jun 19.
Artículo en Inglés | MEDLINE | ID: mdl-37375702

RESUMEN

Ancientino, a complex dietary fiber supplement mimicking the ancient diet, has improved chronic heart failure, kidney function, and constipation. However, its effect on ulcerative colitis is unknown. This study explores the impact of Ancientino on colitis caused by dextran sulfate sodium (DSS) and its mechanisms. Data analyses showed that Ancientino alleviated bodyweight loss, colon shortening and injury, and disease activity index (DAI) score, regulated levels of inflammatory factors (tumor necrosis factor-alpha (TNF-α), interleukin-10 (IL-10), interleukin-1 beta (IL-1ß), and interleukin 6 (IL-6)), reduced intestinal permeability (d-lactate and endotoxin), fluorescein isothiocyanate-dextran (FITC-dextran), and diamine oxidase (DAO), repaired colonic function (ZO-1 and occludin), and suppressed oxidative stress (superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), and malondialdehyde (MDA)) in vivo and in vitro. In short, this study demonstrated that Ancientino alleviates colitis and exerts an anticolitis effect by reducing inflammatory response, suppressing oxidative stress, and repairing intestinal barrier function. Thus, Ancientino may be an effective therapeutic dietary resource for ulcerative colitis.


Asunto(s)
Colitis Ulcerosa , Colitis , Animales , Ratones , Colitis Ulcerosa/tratamiento farmacológico , Dextranos/uso terapéutico , Colitis/tratamiento farmacológico , Inflamación/metabolismo , Colon/metabolismo , Estrés Oxidativo , Interleucina-6/metabolismo , Suplementos Dietéticos , Sulfato de Dextran/efectos adversos , Modelos Animales de Enfermedad , Ratones Endogámicos C57BL
3.
Int J Surg ; 66: 37-47, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-31022519

RESUMEN

BACKGROUND: Although numerous treatments exist for fecal incontinence (FI), no consensus exists on the best treatment strategy. The aim was to review the literature and to compare the clinical outcomes and effectiveness of treatments available for FI. MATERIALS AND METHOD: A systematic literature review was performed, from inception to May 2018, of the following databases: MEDLINE, EMBASE, Science Citation Index Expanded, Cochrane Library. The search terms used were "faecal incontinence" and "treatment". Only randomized controlled trials (RCTs) comparing treatments for FI were considered. A Bayesian network meta-analysis was performed using the Markov chain Monte Carlo method. RESULT: Forty-seven RCTs were included comparing 37 treatments and reporting on 3748 participants. No treatment ranked best or worst with high probability for any outcome of interest. No significant difference was identified between treatments for frequency of FI per week, or in changing the resting pressure, maximum resting pressure, squeeze pressure, and maximum squeeze pressure. Radiofrequency resulted in more adverse events compared to placebo. Sacral nerve stimulation (SNS) and zinc-aluminium improved the fecal incontinence quality of life questionnaire (FIQL) lifestyle, coping, and embarrassment domains compared to placebo. Transcutaneous posterior tibial nerve stimulation (TPTNS) improved the FIQL embarrassment domain compared to placebo. Autologous myoblasts and zinc-aluminium improved the FIQL depression domain compared to placebo. SNS, artificial bowel sphincter (ABS), and zinc-aluminium significantly improved incontinence scores compared to placebo. Injection of non-animal stabilized hyaluronic acid/dextranomer (NASHA/Dx) resulted in more patients with ≥50% reduction in FI episodes compared to placebo. CONCLUSION: SNS, ABS, TPTNS, NASHA/Dx, zinc-aluminium, and autologous myoblasts resulted in isolated improvements in specific outcomes of interest. No difference was identified in incontinence episodes, no treatment ranked best persistently or persistently improved outcomes, and many included treatments did not significantly benefit patients compared to placebo. Large multicentre RCTs with long-term follow-up and standardized inclusion criteria and outcome measures are needed.


Asunto(s)
Incontinencia Fecal/terapia , Teorema de Bayes , Dextranos/uso terapéutico , Terapia por Estimulación Eléctrica/métodos , Incontinencia Fecal/fisiopatología , Humanos , Ácido Hialurónico/uso terapéutico , Metaanálisis en Red , Evaluación de Resultado en la Atención de Salud , Calidad de Vida , Ensayos Clínicos Controlados Aleatorios como Asunto/métodos , Nervio Tibial/fisiopatología
4.
Acta Ophthalmol ; 97(4): 415-421, 2019 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-30284383

RESUMEN

PURPOSE: To compare the effect of corneal collagen cross-linking (CXL) on progressive keratoconus using 0.1% riboflavin with either dextran or methylcellulose as the main supplement. METHODS: In a comparative case series, CXL was performed in 40 patients (40 eyes) using a riboflavin solution containing either dextran (dextran-riboflavin; n = 20) or methylcellulose (methylcellulose-riboflavin; n = 20). Changes in central corneal thickness (CCT), Scheimpflug tomography, maximal keratometry reading (Kmax ), visual acuity (VA) and endothelial cell density (ECD) were recorded. Stromal changes one month after surgery were analysed using optical coherence tomography (OCT) and in vivo confocal microscopy (IVCM). RESULTS: The CCT was significantly higher in the methylcellulose-riboflavin group during the CXL procedure. The IVCM demarcation line depth was 274 ± 80 (SD) µm in the dextran-riboflavin group and 442 ± 80 µm in the methylcellulose-riboflavin group (p < 0.001). Complete absence of keratocytes in the pre-endothelial stroma was found in none of the corneas treated with dextran-riboflavin and in 42% of the corneas treated with methylcellulose-riboflavin. Visibility of the OCT demarcation line was significantly lower in the methylcellulose-riboflavin group. Kmax and corrected distance visual acuity were improved in the methylcellulose-riboflavin group and stable in the dextran-riboflavin group after 2 years. Endothelial cell density (ECD) was stable in both groups. CONCLUSION: We found deeper structural changes in the methylcellulose-riboflavin group than in the dextran-riboflavin group. This may be explained by different riboflavin solution properties and raises safety concerns. The study also indicates improved effect using methylcellulose-riboflavin than dextran-riboflavin, possibly explained by deeper stromal CXL effect.


Asunto(s)
Colágeno/uso terapéutico , Reactivos de Enlaces Cruzados/uso terapéutico , Dextranos/uso terapéutico , Queratocono/tratamiento farmacológico , Metilcelulosa/uso terapéutico , Fotoquimioterapia/métodos , Riboflavina/uso terapéutico , Adolescente , Adulto , Córnea/diagnóstico por imagen , Paquimetría Corneal , Topografía de la Córnea , Quimioterapia Combinada , Femenino , Estudios de Seguimiento , Humanos , Queratocono/diagnóstico , Queratocono/fisiopatología , Masculino , Microscopía Confocal , Fármacos Fotosensibilizantes/uso terapéutico , Sustitutos del Plasma/uso terapéutico , Estudios Prospectivos , Tomografía de Coherencia Óptica , Resultado del Tratamiento , Rayos Ultravioleta , Agudeza Visual , Adulto Joven
5.
J Vis Exp ; (134)2018 04 12.
Artículo en Inglés | MEDLINE | ID: mdl-29708526

RESUMEN

High molecular weight biotinylated dextran amine (BDA) has been used as a highly sensitive neuroanatomical tracer for many decades. Since the quality of its labeling was affected by various factors, here, we provide a refined protocol for the application of high molecular weight BDA for studying optimal neural labeling in the central nervous system. After stereotactic injection of BDA into the ventral posteromedial nucleus (VPM) of the thalamus in the rat through a delicate glass pipette, BDA was stained with fluorescent streptavidin-Alexa (AF) 594 and counterstained with fluorescent Nissl stain AF500/525. On the background of green Nissl staining, the red BDA labeling, including neuronal cell bodies and axonal terminals, was more distinctly demonstrated in the somatosensory cortex. Furthermore, double fluorescent staining for BDA and the calcium-binding protein parvalbumin (PV) was carried out to observe the correlation of BDA labeling and PV-positive interneurons in the cortical target, providing the opportunity to study the local neural circuits and their chemical characteristics. Thus, this refined method is not only suitable for visualizing high quality neural labeling with the high molecular weight BDA through reciprocal neural pathways between the thalamus and cerebral cortex, but also will permit the simultaneous demonstration of other neural markers with fluorescent histochemistry or immunochemistry.


Asunto(s)
Biotina/análogos & derivados , Corteza Cerebral/diagnóstico por imagen , Dextranos/uso terapéutico , Colorantes Fluorescentes/uso terapéutico , Tálamo/diagnóstico por imagen , Animales , Biotina/farmacología , Biotina/uso terapéutico , Dextranos/farmacología , Colorantes Fluorescentes/farmacología , Masculino , Peso Molecular , Ratas
6.
J R Army Med Corps ; 164(2): 69-71, 2018 May.
Artículo en Inglés | MEDLINE | ID: mdl-29431146

RESUMEN

BACKGROUND: Idiopathic sudden sensorineural hearing loss (ISSNHL) is defined as a 30-decibel (dB) loss in hearing over three contiguous frequencies within 3 days. The cause remains unknown, and there is currently no consensus in the literature as to how it is best treated. Conventional treatment in our unit comprises steroids, pentoxyphiline and dextran, with the potential addition of hyperbaric oxygen therapy (HBOT). METHODS: A prospective randomised trial was performed on all soldiers diagnosed with ISSNHL in our institution from 1 January 2007 to 31 December 2016. Participants were randomly allocated to one of two groups. Group A was treated with conventional treatment plus HBOT. Group B was treated with conventional treatment only. Data collection included age, gender, clinical symptoms, pure-tone audiometry results and treatment outcome. RESULTS: 60 participants were enrolled (53 male, 7 female) with ages ranging from 18 to 65 years (mean age of 30.3). No significant differences were observed in the baseline characteristics between the two groups, including gender, age, site, associated symptoms, duration of symptoms and severity of hearing loss. Hearing recovery using Siegel's criteria on days 8 and 13 showed no significant differences between treatment groups. However, the hearing recovery on day 180 was significantly better in those who received the conventional treatment plus HBOT (P<0.05). Additionally, no significant side effects were observed in either group. CONCLUSIONS: HBOT plus existing conventional treatment was associated with a better outcome than conventional treatment alone. We would recommend the addition of HBOT is recommended as a first-line treatment modality for all soldiers presenting with ISSNHL.


Asunto(s)
Pérdida Auditiva Sensorineural/terapia , Oxigenoterapia Hiperbárica , Personal Militar , Enfermedad Aguda , Adolescente , Adulto , Anciano , Terapia Combinada , Dextranos/uso terapéutico , Quimioterapia Combinada , Femenino , Glucocorticoides/uso terapéutico , Audición , Pérdida Auditiva Sensorineural/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Pentoxifilina/uso terapéutico , Sustitutos del Plasma/uso terapéutico , Prednisolona/uso terapéutico , Estudios Prospectivos , Recuperación de la Función , Taiwán , Factores de Tiempo , Resultado del Tratamiento , Vasodilatadores/uso terapéutico , Adulto Joven
7.
Cochrane Database Syst Rev ; 11: CD011764, 2017 11 21.
Artículo en Inglés | MEDLINE | ID: mdl-29161465

RESUMEN

BACKGROUND: Venous thromboembolism (VTE) is a serious but preventable cause of morbidity and mortality. Neuromuscular electrical stimulation systems (NMES) for the prevention of VTE may be beneficial for patients in whom pharmacological or standard mechanical prophylaxis methods are contraindicated or are regarded as unsafe or impractical. Although findings of experimental studies suggest that NMES reduce venous stasis, the clinical utility and effectiveness of NMES in VTE prevention remain controversial. OBJECTIVES: To assess the effectiveness of neuromuscular electrical stimulation in the prevention of venous thromboembolism. SEARCH METHODS: The Cochrane Vascular Group Information Specialist (CIS) searched the Specialised Register (22 March 2017) and the Cochrane Central Register of Controlled Studies (CENTRAL (2017, Issue 2)). The CIS also searched trial registries for details of ongoing and unpublished studies. The review authors searched the bibliographic lists of relevant articles and reviews to look further for potentially eligible trials. SELECTION CRITERIA: We planned to include randomised controlled trials (RCTs) and quasi-randomised trials that compared any form of neuromuscular electrical stimulation as an intervention for VTE prophylaxis (alone or combined with pharmacological or other mechanical methods) versus no prophylaxis and other mechanical or pharmacological methods of VTE prophylaxis. DATA COLLECTION AND ANALYSIS: At least two independent review authors were involved in study selection, data extraction, methodological quality assessment of included studies, and data analysis. We resolved disagreements by discussion between the two review authors. If no agreement could be reached, a third review author acted as an adjudicator. The main outcomes of the review were total deep vein thrombosis (DVT), symptomatic and asymptomatic DVT, pulmonary embolism (PE), total VTE and bleeding (major and minor). The quality of evidence was assessed using the GRADE approach and is indicated in italics. MAIN RESULTS: We included in the review five randomised controlled trials and three quasi-randomised trials, enrolling a total of 904 participants. Among these, four studies included patients undergoing major surgical procedures; one study included patients undergoing surgery for hip fracture under spinal anaesthesia; one study included trauma patients with a contraindication for prophylactic heparin; one study included neurosurgical patients who were operated on under general anaesthesia; and one study included patients with non-functional spinal cord injuries. Overall, eight studies investigated 22 treatment arms. Four studies compared the NMES arm with a no prophylaxis arm, and five studies compared the NMES arm with alternative methods of prophylaxis arms. Alternative methods of prophylaxis included low-dose heparin (5000 IU subcutaneously) - two studies, Dextran 40 - one study, graduated compression stockings (GCS) and intermittent pneumatic compression devices (IPCD) - one study. One study compared combined NMES and low-dose heparin versus no prophylaxis or low-dose heparin alone.We found no clear difference in risks of total DVT (odds ratio (OR) 1.01, 95% confidence interval (CI) 0.60 to 1.70, P = 0.98; 6 studies, 415 participants; low-quality evidence), asymptomatic DVT (OR 1.61, 95% CI 0.40 to 6.43, P = 0.50; 1 study, 89 participants; low-quality evidence), symptomatic DVT (OR 0.40, 95% CI 0.02 to 10.07, P = 0.58; 1 study, 89 participants; low-quality evidence), PE (OR 1.31, 95% CI 0.38 to 4.48, P = 0.67; 2 studies, 126 participants;low-quality evidence), and total VTE (OR 0.92, 95% CI 0.34 to 2.52, P = 0.88; 1 study, 72 participants; low-quality evidence) between prophylaxis with NMES and alternative methods of prophylaxis. None of the studies in this comparison reported bleeding.Compared with no prophylaxis, NMES showed lower risks of total DVT (OR 0.40, 95% CI 0.23 to 0.70, P = 0.02; 4 studies, 576 participants; moderate-quality evidence) and total VTE (OR 0.23, 95% CI 0.09 to 0.59, P = 0.002; 1 study, 77 participants; low-quality evidence). Data show no clear differences in risk of asymptomatic DVT (OR 0.32, 95% CI 0.06 to 1.62, P = 0.17; 1 study, 200 participants; low-quality evidence), symptomatic DVT (OR 0.06, 95% CI 0.00 to 1.36, P = 0.08; 1 study, 160 participants;low-quality evidence), or PE (OR 0.36, 95% CI 0.12 to 1.07, P = 0.07; 1 study, 77 participants; low-quality evidence) between prophylaxis with NMES and no prophylaxis. None of the studies in this comparison reported bleeding.In comparison with low-dose heparin, NMES was associated with higher risk of total DVT (OR 2.78, 95% CI 1.19 to 6.48, P = 0.02; 2 studies, 194 participants; low-quality evidence), but data were inadequate for other comparisons (NMES vs Dextran 40, NMES vs GCS, or NMES vs IPCD) and for other clinical outcomes such as symptomatic or asymptomatic DVT, PE, total VTE, and bleeding in individual comparisons.Overall, we judged the quality of available evidence to be low owing to high or unclear risk of bias and imprecise effect estimates due to small numbers of studies and events. AUTHORS' CONCLUSIONS: Low-quality evidence shows no clear difference in the risk of DVT between NMES and alternative methods of prophylaxis but suggest that NMES may be associated with lower risk of DVT compared with no prophylaxis (moderate-quality evidence) and higher risk of DVT compared with low-dose heparin (low-quality evidence). The best available evidence about the effectiveness of NMES in the prevention of VTE is not adequately robust to allow definitive conclusions. Adequately powered high-quality randomised controlled trials are required to provide adequately robust evidence.


Asunto(s)
Terapia por Estimulación Eléctrica/métodos , Trombosis de la Vena/prevención & control , Anticoagulantes/uso terapéutico , Contraindicaciones de los Medicamentos , Dextranos/uso terapéutico , Heparina/uso terapéutico , Humanos , Aparatos de Compresión Neumática Intermitente , Unión Neuromuscular , Síndrome Postrombótico/prevención & control , Ensayos Clínicos Controlados Aleatorios como Asunto , Medias de Compresión , Tromboembolia Venosa/prevención & control
8.
Am Surg ; 83(2): 134-140, 2017 02 01.
Artículo en Inglés | MEDLINE | ID: mdl-28228199

RESUMEN

The incidence of venous thromboembolism (VTE) in peritoneal malignancies can approach 30 to 50 per cent without prophylaxis. Prophylaxis in cytoreductive surgeries (CRS) presents a challenge to preoperative heparin-based therapy because of an increased risk of coagulopathy and potential for bleeding. Herein, we report the large series of CRS and hyperthermic intraperitoneal chemotherapy receiving dextran-40 prophylaxis. Retrospective chart review of peritoneal malignancies patients undergoing CRS at University of Nebraska Medical Center identified 69 individuals who received dextran-40 between 2010 and 2013. The incidences of VTEs, perioperative bleeding, complications, morbidity, and mortality were determined in-hospital and at 90 days. Of the 69 patients treated, the 30-day VTE rate was 8.7 per cent, and no pulmonary embolisms, bleeding, anaphylactoid reaction, or mortality were observed with dextran usage. The specific VTE events included three upper extremity and three lower extremity VTEs. No additional VTE events were identified between 30 and 90 days. In conclusion, dextran-40 prophylaxis was not associated with any perioperative bleeding events, and the observed incidence of VTE was comparable to reported heparin-based prophylaxis in CRS/hyperthermic intraperitoneal chemotherapy patients. This data supports further exploration of dextran-40 as a VTE prophylactic agent in complex surgical oncology cases.


Asunto(s)
Anticoagulantes/uso terapéutico , Antineoplásicos/administración & dosificación , Procedimientos Quirúrgicos de Citorreducción , Dextranos/uso terapéutico , Hipertermia Inducida , Neoplasias Peritoneales/terapia , Tromboembolia Venosa/prevención & control , Anafilaxia , Anticoagulantes/efectos adversos , Pérdida de Sangre Quirúrgica , Dextranos/efectos adversos , Femenino , Hemorragia , Heparina/efectos adversos , Humanos , Infusiones Parenterales , Complicaciones Intraoperatorias/prevención & control , Masculino , Persona de Mediana Edad , Seudomixoma Peritoneal/terapia , Embolia Pulmonar/prevención & control , Estudios Retrospectivos
9.
Chem Commun (Camb) ; 53(8): 1385-1388, 2017 Jan 24.
Artículo en Inglés | MEDLINE | ID: mdl-28074970

RESUMEN

Partially dextran-coated gold nanoworms enabled the dual-strategic conjugation of peptides and genes. Combinational cancer therapy with photothermal conversion under near-infrared irradiation was shown to be a highly efficient cancer treatment.


Asunto(s)
Antineoplásicos/uso terapéutico , Dextranos/uso terapéutico , Oro/uso terapéutico , Nanopartículas del Metal/química , Neoplasias/tratamiento farmacológico , Anisotropía , Antineoplásicos/química , Terapia Combinada , Dextranos/química , Oro/química , Humanos , Fototerapia , Células Tumorales Cultivadas
10.
Gastroenterol Clin North Am ; 45(2): 217-37, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27261895

RESUMEN

Pelvic floor dysfunction and fecal incontinence is a common and debilitating condition in women, particularly as women age, and often goes under-reported to health care providers. It is important for providers to ask patients about possible symptoms. An algorithm for evaluation and treatment is presented. Current and future therapies are described and discussed.


Asunto(s)
Canal Anal/cirugía , Biorretroalimentación Psicológica , Incontinencia Fecal/terapia , Trastornos del Suelo Pélvico/terapia , Procedimientos de Cirugía Plástica/métodos , Tratamiento de Radiofrecuencia Pulsada , Colostomía , Dextranos/uso terapéutico , Dietoterapia , Terapia por Estimulación Eléctrica , Incontinencia Fecal/diagnóstico , Incontinencia Fecal/fisiopatología , Femenino , Humanos , Ácido Hialurónico/análogos & derivados , Ácido Hialurónico/uso terapéutico , Plexo Lumbosacro , Imanes , Manometría , Trastornos del Suelo Pélvico/diagnóstico , Trastornos del Suelo Pélvico/fisiopatología , Pesarios
11.
Expert Rev Gastroenterol Hepatol ; 9(12): 1577-89, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26414494

RESUMEN

Fecal incontinence is a devastating condition, vastly under-reported, and may affect up to 18% of the population. While conservative management may be efficacious in a large portion of patients, those who are refractory will likely benefit from appropriate surgical intervention. There are a wide variety of surgical approaches to fecal incontinence management, and knowledge and experience are crucial to choosing the appropriate procedure and maximizing functional outcome while minimizing risk. In this article, we provide a comprehensive description of surgical options for fecal incontinence to help the clinician identify an appropriate intervention.


Asunto(s)
Canal Anal/cirugía , Incontinencia Fecal/cirugía , Colostomía , Dextranos/uso terapéutico , Terapia por Estimulación Eléctrica , Incontinencia Fecal/etiología , Incontinencia Fecal/terapia , Humanos , Ácido Hialurónico/uso terapéutico , Ileostomía , Plexo Lumbosacro , Músculo Esquelético/trasplante , Prótesis e Implantes , Terapia por Radiofrecuencia , Nervio Tibial
12.
Pharmacology ; 96(3-4): 192-9, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26316149

RESUMEN

AIM: To evaluate the effect of iron chelators on iron-related pulmonary pathology and oxidative stress in an animal model of ß-thalassemia. METHODS: Pulmonary iron overload was induced in heterozygous ß-globin knockout mice (mußth-3/+, BKO). Over a period of 2 weeks, 180 mg of iron/mouse was loaded by intraperitoneal injection of iron dextran, and subsequently treated daily via intraperitoneal with either deferoxamine (DF) or deferiprone (L1) at an equimolar concentration of iron binding (0.2 and 0.6 µmol/g body weight, respectively) for 7 days. RESULTS: Iron loading resulted in iron deposition in peribronchial regions, septa and also in alveolar macrophages with a grading score of 3. This iron burden resulted in lung epithelial injuries, fibrosis and corresponded with increased lipid peroxidation and decreased tissue catalase activity. Treatment with DF or L1 resulted in a reduction of iron-laden alveolar macrophages and decreased oxidative stress and tissue damage, showing the iron mobilizing ability of both compounds. CONCLUSION: Iron chelation therapy, with DF and L1, may protect against pulmonary damage by sequestering catalytic iron and improving oxidative status. It may be beneficial in the prevention of pulmonary complications in thalassemia.


Asunto(s)
Quelantes del Hierro/uso terapéutico , Sobrecarga de Hierro/tratamiento farmacológico , Sobrecarga de Hierro/etiología , Estrés Oxidativo/efectos de los fármacos , Talasemia beta/complicaciones , Talasemia beta/tratamiento farmacológico , Animales , Antídotos/uso terapéutico , Deferiprona , Deferoxamina/uso terapéutico , Dextranos/uso terapéutico , Femenino , Fibrosis/patología , Sobrecarga de Hierro/patología , Pulmón/metabolismo , Pulmón/patología , Macrófagos Alveolares/efectos de los fármacos , Macrófagos Alveolares/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Ratones Noqueados , Piridonas/farmacología , Mucosa Respiratoria/patología , Globinas beta/genética , Talasemia beta/patología
13.
J Gastrointest Surg ; 19(10): 1910-21, 2015 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-26268955

RESUMEN

INTRODUCTION: Fecal incontinence is a debilitating condition affecting primarily the elderly. Many patients suffer in silence resulting in both underdiagnosis and undertreatment often culminating in an overall poor quality of life. METHODS: We sought to review the etiology, diagnosis, and treatment of fecal incontinence based on current literature. Additionally, newer treatment methods such as Solesta will be evaluated. RESULTS: There are many diagnostic modalities available to assess the degree and severity of the patient's incontinence; however, a thorough history and physical exam is critical. Initial attempts at treatment focus on medical management primarily through stool texture modification with the aid of bulking agents. Failure of medical therapy is often followed by a graded increase in the complexity and invasiveness of the available treatment options. The selection of the most appropriate surgical option, such as overlapping sphincteroplasty and neuromodulation, is multifactorial involving both surgeon and patient-related factors. Neuromodulation has received increased attention in the last decade due to its documented therapeutic success, and newer office-based procedures, such as the Solesta injection, are showing promising results in properly selected patients. Finally, diversion remains an option for select patients who have failed all other therapies. CONCLUSION: The etiology of fecal incontinence is multifactorial, involving a complex interplay between stool consistency and anatomic integrity. The diagnosis and treatment of fecal incontinence continue to evolve and are showing promising results.


Asunto(s)
Incontinencia Fecal/diagnóstico , Incontinencia Fecal/etiología , Incontinencia Fecal/terapia , Dextranos/uso terapéutico , Dieta , Procedimientos Quirúrgicos del Sistema Digestivo , Terapia por Estimulación Eléctrica , Incontinencia Fecal/fisiopatología , Humanos , Ácido Hialurónico/uso terapéutico , Examen Físico , Prótesis e Implantes , Calidad de Vida , Índice de Severidad de la Enfermedad
14.
Bull Exp Biol Med ; 158(1): 112-4, 2014 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-25403410

RESUMEN

Oxidized dextran is suggested for prevention of infection induced by influenza A/H5N1 viruses, methods of its use and doses are determined. Two intravenous injections of dextran 3 and 1 days before experimental infection of outbred mice by influenza A/H5N1 A/goose/Krasnoozerskoye/627/05 virus resulted in a high preventive dose-dependent effect: the mean lifespan was 25% prolonged, the mortality decreased 3-fold.


Asunto(s)
Antivirales/uso terapéutico , Dextranos/uso terapéutico , Subtipo H5N1 del Virus de la Influenza A/efectos de los fármacos , Infecciones por Orthomyxoviridae/prevención & control , Animales , Animales no Consanguíneos , Antivirales/farmacología , Dextranos/farmacología , Evaluación Preclínica de Medicamentos , Ratones , Infecciones por Orthomyxoviridae/virología , Oxidación-Reducción
15.
Surg Endosc ; 28(8): 2277-301, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-24609699

RESUMEN

Fecal incontinence is a frequent and debilitating condition that may result from a multitude of different causes. Treatment is often challenging and needs to be individualized. During the last several years, new technologies have been developed, and others are emerging from clinical trials to commercialization. Although their specific roles in the management of fecal incontinence have not yet been completely defined, surgeons have access to them and patients may request them. The purpose of this project is to put into perspective, for both the patient and the practitioner, the relative positions of new and emerging technologies in order to propose a treatment algorithm.


Asunto(s)
Incontinencia Fecal/terapia , Canal Anal/inervación , Canal Anal/cirugía , Órganos Artificiales , Ablación por Catéter , Descompresión Quirúrgica , Dextranos/uso terapéutico , Procedimientos Quirúrgicos del Sistema Digestivo/métodos , Terapia por Estimulación Eléctrica , Nervio Femoral/cirugía , Fármacos Gastrointestinales/uso terapéutico , Humanos , Ácido Hialurónico/uso terapéutico , Inyecciones , Plexo Lumbosacro , Imanes , Microesferas , Síndromes de Compresión Nerviosa/cirugía , Transferencia de Nervios , Nervio Pudendo/cirugía , Mecanismo de Reembolso , Mallas Quirúrgicas , Nervio Tibial
16.
Invest Radiol ; 48(12): 826-33, 2013 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-23835597

RESUMEN

PURPOSE: The purpose of this study was to evaluate the feasibility and the therapeutic efficacy of a novel drug-delivery system that uses superparamagnetic iron oxide (SPIO) and iodized oil (IO) to improve the selective intra-arterial (IA) drug delivery to an experimentally induced hepatic tumor. MATERIALS AND METHODS: This animal study was approved by our institutional animal care and use committee. Fifteen rabbits with hepatic VX2 carcinomas were treated with IA delivery of 4 different agents: doxorubicin alone (group A, n = 3), doxorubicin/IO (group B, n = 3), a doxorubicin/SPIO complex (group C, n = 4), and a doxorubicin/SPIO/IO complex (group D, n = 5). The infused doxorubicin dose was 1 mg for all groups. The serum doxorubicin concentration was measured at 0, 5, 30, 60, and 120 minutes after the delivery. To assess the distribution of the SPIO, magnetic resonance (MR) scans were performed at day 7 after the delivery, when computed tomographic scans were performed in addition to MR in group B and D to assess the distribution of IO. After the completion of follow-up imaging, all the animals were euthanized to measure the intratumoral doxorubicin concentration and to assess tumor viability through pathologic examination. RESULTS: Groups C and D demonstrated significantly lower MR signal intensities, which inversely corresponded to SPIO deposition, in the tumor areas than did groups A and B. Group D exhibited the lowest serum doxorubicin concentration at all time points up to 180 minutes after the delivery, suggesting minimal passage of doxorubicin into the systemic circulation. The intratumoral doxorubicin concentrations were 72.4 ng/g for group A, 142.0 ng/g for group B, 264.1 ng/g for group C, and 679.6 ng/g for group D. The proportion of viable tumor cells were 65.3% for group A, 1.3% for group B, 17.0% for group C, and 0.1% for group D. CONCLUSIONS: The drug-delivery system developed using SPIO and IO can result in better drug targeting when it is used for IA delivery to liver cancer. The results of this study warrant further investigation of this potential clinical treatment of advanced liver cancer.


Asunto(s)
Dextranos/química , Doxorrubicina/administración & dosificación , Doxorrubicina/farmacocinética , Aceite Yodado/química , Neoplasias Hepáticas/tratamiento farmacológico , Neoplasias Hepáticas/metabolismo , Nanopartículas de Magnetita/química , Nanocápsulas/química , Animales , Antibióticos Antineoplásicos/administración & dosificación , Antibióticos Antineoplásicos/farmacocinética , Línea Celular Tumoral , Dextranos/uso terapéutico , Relación Dosis-Respuesta a Droga , Evaluación Preclínica de Medicamentos , Inyecciones Intraarteriales , Aceite Yodado/uso terapéutico , Neoplasias Hepáticas/patología , Nanopartículas de Magnetita/uso terapéutico , Nanocápsulas/uso terapéutico , Conejos , Resultado del Tratamiento
17.
Int J Pharm ; 440(2): 188-94, 2013 Jan 20.
Artículo en Inglés | MEDLINE | ID: mdl-22917746

RESUMEN

In this work, the supercritical assisted atomisation (SAA) is proposed, for the first time, for the production of topical carrier microsystems based on alginate-pectin blend. Gentamicin sulphate (GS) was loaded as high soluble and hygroscopic antibiotic model with poor flowability. Particularly, different water solutions of GS/alginate/pectin were processed by SAA to produce spherical microparticles (GAP) of narrow size (about 2 µm). GS loading was varied between 20% and 33% (w/w) with an encapsulation efficiency reaching about 100%. The micronised powders also showed high flow properties, good stability and constant water content after 90 days in accelerated storage conditions. The release profiles of the encapsulated drug were monitored using vertical diffusion Franz cells to evaluate the application of GAP microsystems as self-consistent powder formulation or in specific fibres or gels for wound dressing. All formulations showed an initial burst effect in the first 6h of application (40-65% of GS loaded), and in particular GAP4 produced with a GS/alginate/pectin ratio of 1:3:1, exhibited the ability to release GS continuously over 6 days. Antimicrobial tests against Staphylococcus aureus indicated that GS antibiotic activity was preserved at 6 days and higher than pure GS at 12 and 24 days for all SAA formulations, especially for GAP1.


Asunto(s)
Antibacterianos/administración & dosificación , Cromatografía con Fluido Supercrítico/métodos , Dextranos/administración & dosificación , Diseño de Fármacos , Gentamicinas/administración & dosificación , Gentamicinas/farmacocinética , Infección de Heridas/tratamiento farmacológico , Administración Cutánea , Antibacterianos/farmacocinética , Antibacterianos/uso terapéutico , Disponibilidad Biológica , Cromatografía con Fluido Supercrítico/instrumentación , Dextranos/uso terapéutico , Portadores de Fármacos/administración & dosificación , Portadores de Fármacos/uso terapéutico , Estabilidad de Medicamentos , Gentamicinas/uso terapéutico , Pruebas de Sensibilidad Microbiana/métodos , Tamaño de la Partícula , Polvos/administración & dosificación , Polvos/uso terapéutico , Staphylococcus aureus/efectos de los fármacos
18.
J Emerg Med ; 43(3): 468-71, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22497894

RESUMEN

BACKGROUND: Meprobamate tablets contain microcrystalline cellulose, a potent embolic agent that has been shown to cause gangrene in animal studies. Microvascular embolization caused by microcrystalline cellulose can contribute to the ischemic process. OBJECTIVE: We report a case of acute hand ischemia after accidental intra-arterial injection of crushed meprobamate powder in a 23-year-old male drug abuser. CASE REPORT: The distal tips of the patient's right thumb, index finger, ring finger, and little finger continued to develop gangrene despite medical therapy with heparinization, low molecular-weight dextran infusion, corticosteroid administration, and hyperbaric oxygen therapy. CONCLUSION: We believe this is the first case of acute limb ischemia caused by intra-arterial injection of meprobamate powder documented in humans. Emergency physicians should be aware that accidental intra-arterial injection of crushed oral drug formulations is potentially limb threatening and prompt recognition of similar clinical scenarios is of vital importance.


Asunto(s)
Mano/irrigación sanguínea , Hipnóticos y Sedantes/efectos adversos , Isquemia/inducido químicamente , Meprobamato/efectos adversos , Enfermedad Aguda , Adulto , Amputación Quirúrgica , Antiinflamatorios/uso terapéutico , Anticoagulantes/uso terapéutico , Dexametasona/uso terapéutico , Dextranos/uso terapéutico , Consumidores de Drogas , Mano/cirugía , Humanos , Oxigenoterapia Hiperbárica , Hipnóticos y Sedantes/administración & dosificación , Inyecciones Intraarteriales/efectos adversos , Isquemia/terapia , Masculino , Meprobamato/administración & dosificación , Polvos , Abuso de Sustancias por Vía Intravenosa/complicaciones , Adulto Joven
19.
Am J Nephrol ; 35(1): 69-74, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22189072

RESUMEN

INTRODUCTION: The Renal NSF advocates correction of anaemia in chronic kidney disease patients. Oral iron is often insufficient, while intravenous supplementation replenishes and maintains iron stores. There is a need to administer high doses of iron in a single rapid infusion to enable efficient costs, effective utilisation of time for patients and staff and optimal use of resources. METHODS: We performed a prospective study of consecutive patients referred for iron dextran (Cosmofer) therapy. This was administered over 2 h 40 min compared with the normal regime of 4-6 h. Blood pressure was recorded throughout administration. Adverse drug reactions were recorded over 2 weeks. Serum ferritin, haemoglobin and estimated glomerular filtration rate were measured at baseline and 3 months. RESULTS: One hundred patients (59 male, mean age 69 years), received a median dose of 1,000 mg Cosmofer in a median time of 2 h 40 min. Mean serum ferritin rose from 178 at baseline to 413 µg/l (p < 0.001). Mean haemoglobin rose by 1.5 g/dl (p < 0.001). There was no decline in estimated glomerular filtration rate after 3 months. No adverse reactions were noted. CONCLUSION: We demonstrated that accelerated administration of iron dextran is safe and effective with no short-term effects on renal function. This resulted in a time saving of approximately 67 hours.


Asunto(s)
Dextranos/uso terapéutico , Fallo Renal Crónico/tratamiento farmacológico , Adolescente , Adulto , Anciano , Dextranos/administración & dosificación , Femenino , Humanos , Infusiones Intravenosas , Masculino , Persona de Mediana Edad , Modelos Estadísticos , Peso Molecular , Proyectos Piloto , Estudios Prospectivos , Factores de Tiempo
20.
Zhongguo Zhong Xi Yi Jie He Za Zhi ; 30(10): 1049-51, 2010 Oct.
Artículo en Chino | MEDLINE | ID: mdl-21066888

RESUMEN

OBJECTIVE: To investigate the effect of compound Danshen injection combined with prostaglandin E1 low molecular weight heparin calcium to dextran-40 preventing hepatic veno-occlusive disease (HVOD) after hematopoietic stem cell transplantation (HSCT). METHODS: A total of 520 patients who received HSCT in the authors' hospital from May 1998 and December 2009 were subjected, among whom 231 patients received autologous peripheral blood stem cell transplantation, 125 received HLA-identical sibling HSCT, 49 received HLA-identical/mismatched unrelated HSCT and 115 received HLA-haplotype HSCT. All patients were treated by intravenous dripping of CSI 40-60 mL, dextran-40 250-500 mL, prostaglandin-E1 40-60 microg, and subcutaneous injection of low molecular weight heparin calcium 3 000-5 000 IU every day, the preventive effect on HVOD after HSCT was observed. RESULTS: HVOD occurred and caused death only in 1 case of the 520 patients observed, the incidence was 0.19%. Neither obvious adverse reaction nor coagulation disorder was found. CONCLUSION: Compound Danshen Injection combined with prostaglandin E1, low molecular weight heparin calcium and dextran-40 is a safe and effective protocol for the prevention of HVOD after HSCT.


Asunto(s)
Alprostadil/uso terapéutico , Medicamentos Herbarios Chinos/uso terapéutico , Trasplante de Células Madre Hematopoyéticas/efectos adversos , Heparina de Bajo-Peso-Molecular/uso terapéutico , Enfermedad Veno-Oclusiva Hepática/prevención & control , Fenantrolinas/uso terapéutico , Adolescente , Adulto , Niño , Preescolar , Terapia Combinada , Dextranos/uso terapéutico , Femenino , Enfermedad Veno-Oclusiva Hepática/etiología , Humanos , Masculino , Persona de Mediana Edad , Salvia miltiorrhiza
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