Steroid

类固醇
  • 文章类型: Case Reports
    一名86岁的女性腿部水肿,运动时呼吸困难,入院。胸部计算机断层扫描(CT)显示前纵隔肿块伴心包浸润。支气管内超声引导下经支气管针吸活检(EBUS-TBNA)的组织学检查可诊断为Masaoka期IVaB2型胸腺瘤。为了减轻痛苦,放疗(32Gy/16次)和泼尼松龙(30mg/天)并逐渐减少。治疗后,心包积液和肿瘤大小均减小。类固醇和放射疗法的联合治疗可能对治疗胸腺瘤有效。
    An 86-year-old woman with leg edema and dyspnea on exertion was admitted to our hospital. Chest computed tomography (CT) revealed a mass in the anterior mediastinum with pericardial invasion. Histological examination with endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) led to the diagnosis of Masaoka stage IVa type B2 thymoma. For palliation, radiotherapy (32 Gy/16 fractions) and prednisolone (30 mg/day) were administered and tapered. After treatment, both the pericardial effusion and tumour size decreased. Combination therapy with steroids and radiotherapy may be effective for treating thymomas.
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  • 文章类型: Journal Article
    目的:小儿白内障手术后使用糖皮质激素治疗对预防炎症至关重要,但可能会导致继发性青光眼,和下丘脑-垂体-肾上腺轴抑制。我们希望比较小儿白内障手术后高剂量和低剂量糖皮质激素治疗后的青光眼结局。
    方法:这项队列研究包括在10岁之前接受白内障手术的丹麦儿童,接受低剂量或高剂量的术后糖皮质激素治疗。病例识别和标准化数据集的收集是回顾性的,从2010年1月1日至2016年12月31日,以及此后的预期,直到2021年12月31日。高剂量治疗包括0.5-1.0mg结膜下储库地塞米松或甲基强的松龙,随后6-8滴地塞米松1周,每周减少一滴。低剂量治疗包括6滴3天,随后是3滴18天。比较两组持续(>3个月)高眼压或青光眼。
    结果:总体而言,267名儿童(388只眼)被纳入研究。95名儿童(133只眼)接受了大剂量治疗,中位随访时间为89个月(IQR:57.2-107.4)。而173名儿童(255只眼)接受了低剂量治疗,中位随访时间为40.5个月(IQR:22.9-60.4).生存曲线显示,对于轴长≥18mm的儿童,低剂量组的青光眼风险较低。
    结论:低剂量糖皮质激素治疗与眼轴长度≥18mm的儿童青光眼风险降低相关。在眼睛较短的儿童中未观察到相同的效果。大剂量糖皮质激素应限制在接受白内障手术的儿童中。
    OBJECTIVE: Treatment with glucocorticoids following paediatric cataract surgery is crucial to prevent inflammation, but may lead to secondary glaucoma, and hypothalamic-pituitary-adrenal axis suppression. We wish to compare glaucoma outcomes following high-dose and low-dose glucocorticoid treatment after paediatric cataract surgery.
    METHODS: This cohort study included Danish children undergoing cataract surgery before 10 years of age, receiving either a low-dose or high-dose postoperative glucocorticoid treatment. Case identification and collection of a standardized dataset were retrospective, from 1 January 2010 to 31 December 2016, and prospective thereafter, until 31 December 2021. High-dose treatment included 0.5-1.0 mg subconjunctival depot dexamethasone or methylprednisolone, followed by 6-8 drops of dexamethasone for 1 week, tapered by one drop weekly. Low-dose treatment included 6 drops for 3 days, followed by 3 drops for 18 days. Sustained (>3 months) ocular hypertension or glaucoma was compared between the two groups.
    RESULTS: Overall, 267 children (388 eyes) were included in the study. Ninety-five children (133 eyes) had received high-dose treatment and had a median follow-up time of 89 months (IQR: 57.2-107.4), while 173 children (255 eyes) had received the low-dose treatment and had a median follow-up time of 40.5 months (IQR: 22.9-60.4). Survival curves showed a lower risk of glaucoma in the low-dose group for children with axial lengths ≥18 mm.
    CONCLUSIONS: Low-dose glucocorticoid treatment was associated with a lower risk of glaucoma in children with axial lengths ≥18 mm. The same effect was not observed in children with shorter eyes. High-dose glucocorticoid should be limited in children undergoing cataract surgery.
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  • 文章类型: Journal Article
    背景:由于担心心肌损伤,目前的成人心脏手术指南建议不要在体外循环(CPB)期间常规使用预防性静脉注射皮质类固醇,尽管它们有可能减少术后心房颤动。传统上,1,000mg甲基强的松龙的高剂量用于减轻与CPB相关的炎症反应.我们的机构与指南建议保持一致,并逐渐减少甲基强的松龙的剂量;因此,我们重新评估了对术后临床结局的影响.
    方法:我们的研究回顾了在2019年6月至2022年5月期间进行的1680例成人心脏手术中的1341例病例,这些病例排除了非体外循环手术的病例。心室辅助装置植入,心脏移植,需要全身循环停止的主动脉手术。该研究及时排序,包括2018年的基线数据,以及2019年以来的其他三个时期,以分析三种不同剂量的甲基强的松龙的影响:0mg,500毫克,和1000毫克。我们评估了甲基强的松龙给药的年度趋势,并比较了各组的发病率和死亡率。
    结果:我们观察到类固醇使用显着下降,到第3期,无类固醇手术从23%增加到66.5%。尽管减少了类固醇的使用,我们的研究显示死亡率没有增加,新发心房颤动,急性肾损伤,与基线数据相比,脑血管事件和通气时间延长。值得注意的是,无类固醇组手术部位感染率较低.
    结论:数据表明,在CPB期间减少或停用类固醇可以在不影响患者预后的情况下进行。这可以支持在成人心脏手术中更保守地使用类固醇的过渡,符合当前的指导方针,并有可能减少某些术后并发症。
    BACKGROUND: Current adult cardiac surgery guidelines recommend against the routine use of prophylactic intravenous corticosteroids during cardiopulmonary bypass (CPB) due to concerns about myocardial injury, despite their potential to reduce postoperative atrial fibrillation. Traditionally, a high dose of 1,000 mg of methylprednisolone was used to attenuate the inflammatory response associated with CPB. Our institution aligned with guideline recommendations and gradually reduced methylprednisolone dosages; thus, we reevaluated the impact on postoperative clinical outcomes.
    METHODS: Our study reviewed 1341 cases from a total of 1680 adult cardiac surgeries performed between June 2019 and May 2022 after excluding cases with off-pump procedures, ventricular assist device implantations, heart transplants, and aortic surgeries requiring systemic circulatory arrest. The study timely sorted periods including a baseline data from 2018, and other three periods since 2019 to analyze the effects of three different methylprednisolone dosage: 0 mg, 500 mg, and 1000 mg. We assessed the annual trends in methylprednisolone administration and compared morbidity and mortality rates across the groups.
    RESULTS: We observed a significant decline in steroid use, with no-steroid surgeries increasing from 23% to 66.5% by period 3. Despite the decreased use of steroids, our study showed no increase in mortality, new-onset atrial fibrillation, acute kidney injury, cerebrovascular event and prolonged ventilation when compared to baseline data. Notably, less surgical site infection rate was observed in the no-steroid group.
    CONCLUSIONS: The data indicates that a reduction or discontinuation of steroids during CPB can be performed without compromising patient outcomes. This could support a transition towards a more conservative use of steroids in adult cardiac surgery, aligning with current guidelines, and potentially reducing certain postoperative complications.
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  • 文章类型: Journal Article
    本研究中患者的纳入标准不一致,特别是在区分Fuchs葡萄膜炎和疱疹性葡萄膜炎与Posner-Schlossman综合征时,需要明确的纳入标准.CMV前葡萄膜炎和Posner-Schlossman综合征可能不是同一种疾病,CMV可能只作为波斯纳-施洛斯曼综合征的触发因素,轻度眼前节炎症的临床表现主要由自身免疫因子介导的炎症反应引起。尽管抗病毒药物在Posner-Schlossman综合征的治疗中很重要,其他治疗方法,特别是局部类固醇的作用不容忽视。
    The inclusion criteria of patients in this study were inconsistent especially in distinguishing Fuchs\' uveitis and herpetic uveitis from Posner-Schlossman syndrome, indicating well-defined inclusion criteria were needed. CMV anterior uveitis and Posner-Schlossman syndrome may not be the same disease, CMV may only act as a triggering factor for Posner-Schlossman syndrome, and the clinical manifestations of mild anterior segment inflammation were mainly caused by inflammatory reactions mediated by autoimmune factors. Although the antiviral medication was important in the treatment of Posner-Schlossman syndrome, the role of other treatment methods especially topical steroids should not be ignored.
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  • 文章类型: Journal Article
    这项研究分析了甲基强的松龙改善黄疸的有效性,胆红素水平,肝功能检查,和婴儿胆汁淤积的炎症生物标志物。
    随机化,主动控制,平行组试验(ISRCTN45080388注册)于2022年11月至2023年5月在Soetomo综合学术医院进行,泗水,印度尼西亚,婴儿胆汁淤积。Soetomo博士综合学术医院伦理委员会,泗水批准了研究方案。14天至3个月大的婴儿,胆汁淤积,其次是大便,深色尿液,和肝肿大纳入试验.参与者被随机分配给甲基强的松龙2mg/kg/天,每天两次,或安慰剂,每天两次,持续两周。所有患者每日三次服用熊去氧胆酸(10mg/kg)。临床检查和实验室测量(直接和总胆红素,天冬氨酸转氨酶(AST),丙氨酸转氨酶(ALT),γ-谷氨酰转移酶(GGT),和炎症生物标志物)在基线和治疗2周后进行。炎症生物标志物的测量(IL-2,IL-4,IL-6,IL-10,IFN-γ,TGF-β,和ANCA)使用酶联免疫测定法进行。检查数据分布是否正常。使用SPSSver进行分析。21,p显著<0.05。
    总共,40名参与者被随机分为甲基强的松龙(n=20;平均年龄8.39±3.11周)和安慰剂(n=18;2退出;平均年龄8.98±2.80周)组。在基线,甲基强的松龙治疗组和安慰剂组在性别上有显著差异(p=0.02),但在临床上没有显著差异,实验室检查,或炎性生物标志物水平。甲基强的松龙组直接胆红素8.36±4.84mg/dL;总胆红素10.40(2.70-33.25)mg/dL;AST187.05(42.00-911.00)U/L;ALT170.43±134.43U/L;IL-2171.29(73.70-378.57)ng/L;IL-4119.57±59.69L/IFN0.66ng/L;经过两周的治疗,直接胆红素,总胆红素,AST,甲基强的松龙组的IL-10和IFN-γ水平显著低于安慰剂组(p<0.05)。未报告严重不良事件。
    甲基强的松龙可有效降低2周胆红素水平。这些结果支持免疫过程参与胆汁淤积的假设。需要更大样本量的进一步研究来确认甲基强的松龙在胆汁淤积中的胆管抗炎作用,这是新疗法预防胆汁淤积到胆道闭锁的免疫病理学过程的机会。
    UNASSIGNED: This study analyzed the effectiveness of methylprednisolone in improving jaundice, bilirubin levels, liver function tests, and inflammatory biomarkers in infants with cholestasis.
    UNASSIGNED: The randomized, actively controlled, parallel-group trial (ISRCTN45080388 registry) was conducted from November 2022 to May 2023 in Dr. Soetomo General Academic Hospital, Surabaya, Indonesia, on infants with cholestasis. The ethics committee of Dr. Soetomo General Academic Hospital, Surabaya approved the study protocol. Infants 14 days to 3 months old, with cholestasis followed by acholic stool, dark urine, and hepatomegaly were included in the trial. Participants were randomly assigned to methylprednisolone 2 mg/kg/day twice daily or to placebo twice daily for two weeks. Ursodeoxycholic acid (10 mg/kg) was administered to all patients thrice daily. Clinical examination and laboratory measurements (direct and total bilirubin, Aspartate aminotransferase (AST), Alanine transaminase (ALT), Gamma-glutamyl transferase (GGT), and inflammatory biomarker) were performed at baseline and after 2-week treatment. Measurement of inflammatory biomarkers (IL-2, IL-4, IL-6, IL-10, IFN-γ, TGF-β, and ANCA) was performed using enzyme-linked immunoassays. Data distribution was checked for normality. Analysis was carried out using SPSS ver. 21 with p significant <0.05.
    UNASSIGNED: In total, 40 participants were randomized to methylprednisolone (n = 20; mean age 8.39 ± 3.11 weeks) and placebo (n = 18; 2 drop out; mean age 8.98 ± 2.80 weeks) groups. At baseline, the methylprednisolone treatment and placebo groups significantly differed in gender (p = 0.02) but not in clinical, laboratory examination, or inflammatory biomarker levels. The methylprednisolone group had direct bilirubin 8.36 ± 4.84 mg/dL; total bilirubin 10.40 (2.70-33.25) mg/dL; AST 187.05 (42.00-911.00) U/L; ALT 170.43 ± 134.43 U/L; IL-2 171.29 (73.70-378.57) ng/L; IL-4 119.57 ± 59.69 ng/L; IL-6 71.74 ± 29.83 ng/L; IL-10 138.15 ± 70.62 ng/L; IFN-γ 42.54 ± 12.17 ng/L; TGF-β 316.58 (163.68-606.16) ng/L; ANCA 1.70 (0.66-3.25) ng/L. After two weeks of treatment, direct bilirubin, total bilirubin, AST, IL-10, and IFN-γ levels were significantly lower in the methylprednisolone group (p < 0.05) than those in the placebo group. No serious adverse events were reported.
    UNASSIGNED: Methylprednisolone was efficacious in reducing 2-week bilirubin levels. These results support the hypothesis that the immunological process is involved in cholestasis. Further studies with larger sample sizes are needed to confirm the bile duct anti-inflammatory effect of methylprednisolone in cholestasis as an opportunity for new therapies to prevent the immunopathological process of cholestasis to biliary atresia.
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  • 文章类型: Journal Article
    目的:我们进行了动物和类器官研究,以评估类固醇对胆道闭锁(BA)的抗纤维化作用及其潜在的病理机制。
    方法:通过在出生后第1天用恒河猴轮状病毒(RRV)接种小鼠来创建BA动物模型。从第21天到第34天,他们接受20μl磷酸盐缓冲盐水(PBS)或类固醇。在第34天,收集其血清样品的激素标记物。坏死,评估肝纤维化和CK19表达。开发肝类器官,并分析其形态以及大量RNA测序数据。
    结果:24只小鼠在注射RRV后出现BA特征,并平均分为类固醇和PBS组。在第34天,类固醇组的体重增加显著高于PBS组(p<0.0001)。PBS组中的所有小鼠发生肝纤维化,但类固醇组中只有一只小鼠发生肝纤维化。类固醇组血清胆红素和肝实质酶显著降低。两组肝类器官的形态存在差异。在类固醇组和PBS组之间共发现6359个差异表达基因。
    结论:根据我们从RRV诱导的BA动物和类器官模型获得的发现,类固醇具有减轻BA肝纤维化的潜力。
    OBJECTIVE: We performed animal and organoid study to evaluate the anti-fibrotic effect of steroid on biliary atresia (BA) and the underlying patho-mechanism.
    METHODS: BA animal models were created by inoculation of mice on post-natal day 1 with rhesus rotavirus (RRV). They received either 20 µl phosphate-buffered saline (PBS) or steroid from day 21 to day 34. On day 34, their serum samples were collected for hormonal markers. Necrosis, fibrosis and CK 19 expression in the liver were evaluated. Liver organoids were developed and their morphology as well as bulk RNA sequencing data were analyzed.
    RESULTS: Twenty-four mice developed BA features after RRV injection and were equally divided into steroid and PBS groups. On day 34, the weight gain of steroid group increased significantly than PBS group (p < 0.0001). All mice in the PBS group developed liver fibrosis but only one mouse in the steroid group did. Serum bilirubin and liver parenchymal enzymes were significantly lower in steroid group. The morphology of liver organoids were different between the two groups. A total of 6359 differentially expressed genes were found between steroid group and PBS group.
    CONCLUSIONS: Based on our findings obtained from RRV-induced BA animal and organoid models, steroid has the potential to mitigate liver fibrosis in BA.
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  • 文章类型: Journal Article
    背景:免疫性血小板减少性紫癜,复发性自身免疫性疾病,以血小板减少为特征,紫癜和出血性发作,该疾病发病机理的主要因素是抗血小板的自身抗体。自1950年代以来,一线治疗一直是对血小板减少有间接和直接作用的糖皮质激素.尽管在先前的研究中已经研究了与诊断时免疫性血小板减少性紫癜的慢性化相关的特征,在文献中没有发现研究一线类固醇治疗的反应与病程之间的关系,本研究的目的。
    方法:本回顾性研究,单中心研究回顾了2012年9月至9月在临床血液科诊断为免疫性血小板减少性紫癜患者的电子档案,Selcuk大学医学院2022。血小板计数≤30×109/L的患者的外周血涂片证实了血小板计数。根据免疫性血小板减少性紫癜出血评分评估患者在诊断时的出血状况。患者对治疗的反应分为三组:血小板计数≤30×109/L定义为无反应,血小板计数30-100×109/L被定义为部分反应,血小板计数>100×109/L定义为完全缓解。随后,部分缓解或完全缓解组的患者分为两个亚组:缓解时间少于或超过6个月的患者.
    结果:共有100名患者被纳入研究;73%为年轻(19-65岁),27%为老年(>65岁)。大多数患者为女性(69%)。41例患者住院,无出血。一线治疗的完全缓解率为61%。在反应和缓解时间方面,一线治疗中给予的药物之间没有显着差异。
    结论:免疫性血小板减少性紫癜治疗的主要目的是防止严重出血,而不是使血小板计数达到正常值。糖皮质激素,治疗的第一步,提供高响应率。在对治疗的反应和长期缓解方面,糖皮质激素药物之间没有显着差异。在选择糖皮质激素药物时要考虑的要点是副作用,易于管理和个体化治疗。
    BACKGROUND: Immune thrombocytopenic purpura, a recurrent autoimmune disease, is characterized by thrombocytopenia, purpura and hemorrhagic episodes with the main factor in the pathogenesis of this disease being autoantibodies against platelets. Since the 1950s, first-line treatment has been glucocorticoids that have indirect and direct effects on thrombocytopenia. Although the characteristics associated with the chronicization of immune thrombocytopenic purpura at the time of diagnosis have been investigated in previous studies, no study was found in the literature investigating the relationship between the response to first-line steroid treatment and the course of the disease, the aim of this study.
    METHODS: This retrospective, single center study revisited electronic files of patients with a diagnosis of immune thrombocytopenic purpura between September 2012 and September at the Department of Clinical Hematology, Selcuk University Faculty of Medicine 2022. The platelet count had been confirmed by peripheral blood smears of patients with a platelet count ≤30 × 109/L. The bleeding status of patients at the time of diagnosis was evaluated according to the immune thrombocytopenic purpura bleeding score. Patient responses to treatment were categorized in three groups: a platelet count ≤30 × 109/L was defined as no-response, a platelet count of 30-100 × 109/L was defined as partial response, and a platelet count >100 × 109/L was defined as complete response. Subsequently, patients in the partial or complete response groups were divided into two subgroups: patients who remained in remission for less than or more than six months.
    RESULTS: A total of 100 patients were included in the study; 73 % were in the young (19-65 years old) and 27 % in the old (>65 years old) age group. Most of the patients were female (69 %). Forty-one patients were hospitalized without bleeding. The complete response rate to first-line treatment was 61 %. There was no significant difference between the agents given in first-line treatment in terms of response and length of remission.
    CONCLUSIONS: The main purpose of immune thrombocytopenic purpura treatment is to prevent severe bleeding rather than bringing the platelet count to normal values. Glucocorticoids, the first step of treatment, provide high response rates. There is no significant difference between glucocorticoid agents in terms of response to treatment and long-term remission. The points to be considered in the selection of glucocorticoid agents are the side effect profiles, ease of administration and individualization of treatment.
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  • 文章类型: Case Reports
    类固醇通常用于医疗目的。虽然打嗝是类固醇治疗的公认副作用,我们没有发现任何打嗝干扰放疗进展的报告。介绍了一例在射波刀放射治疗(CKR)期间地塞米松(DEX)引起的打嗝(DIH)。一名42岁的I型神经纤维瘤病患者有起源于右股骨的恶性外周神经鞘瘤的病史。我们开始以4mg/天的剂量口服DEX进行CKR,以治疗颅骨转移和原发性病变的复发。DEX剂量增加后四天出现严重打嗝。CKR启动后六天停止DEX,在接下来的四天里,打嗝消退了。然而,CKR手术是不可能的,由于患者的头部和大腿病变的加重肿胀,这阻碍了网状面罩和身体固定装置的正确配合。开始静脉(IV)DEX6.6mg/天,由于病变肿胀减少,这使得CKR恢复。由于过渡到IVDEX后没有打嗝,因此完成了CKR。当口服时,DIH甚至可以在4mg/天的剂量下发生。我们的案例表明在放疗期间识别DIH的重要性。将给药从口服转换为IVDEX可能是处理DIH的一种选择。
    Steroids are commonly used for medical purposes. While hiccups are a recognized side effect of steroid therapy, we have not found any reports of hiccups interfering with the progress of radiotherapy. A case of dexamethasone (DEX)-induced hiccups (DIH) during CyberKnife radiotherapy (CKR) is presented. A 42-year-old man with neurofibromatosis type I had a history of malignant peripheral schwannomas originating in the right femur. We started to perform CKR with oral DEX at an increased dose of 4 mg/day for the recurrence of cranial metastasis and primary lesions. Severe hiccups developed four days after the increased DEX dose. DEX was stopped six days after CKR initiation, and the hiccups subsided over the next four days. However, the CKR procedure was not possible due to the patient\'s worsening swelling of the head and thigh lesions, which prevented the proper fit of the mesh face mask and body fixation device. Intravenous (IV) DEX 6.6 mg/day was initiated, which allowed the resumption of CKR due to reduced swelling of the lesions. The CKR was completed due to the absence of hiccups following the transition to IV DEX. DIH could occur even at a dosage of 4 mg/day when taken orally. Our case suggests the significance of recognizing DIH during radiotherapy. Switching the administration from oral to IV DEX may be an option for dealing with DIH.
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  • 文章类型: Journal Article
    超声(US)引导的颈选择性神经根阻滞(CSNRB)手术越来越多地作为常规透视(FL)引导的硬膜外注射治疗颈根痛的替代方法。这项研究的目的是比较US引导的CSNRB与FL引导的颈椎板间硬膜外类固醇注射(IL-CESI)治疗颈椎神经根疼痛的有效性。共有60例因单节椎间盘突出症引起的颈根性疼痛患者被随机分为FL组或US组。数字评级量表,在治疗前、治疗后第1、3和6个月评估短表36和颈部残疾指数。手术时间,并发症,止痛药消费,并记录患者满意度.患者经历了疼痛的显着改善,残疾,术后6个月的生活质量评分(p<0.001)。治疗成功率在IL-CESI组的56.6%和CSNRB组的50%中实现,在研究组之间没有任何显著差异(p=0.617)。US引导的CSNRB与FL引导的IL-CESI治疗颈根性疼痛同样有效。除了没有辐射暴露和需要较少的手术时间。
    Ultrasound (US)-guided cervical selective nerve root block (CSNRB) procedures are increasingly being performed as an alternative to conventional fluoroscopy (FL)-guided epidural injections for the treatment of cervical radicular pain. The aim of this study was to compare the effectiveness of US-guided CSNRB versus FL-guided interlaminar cervical epidural steroid injection (IL-CESI) for cervical radicular pain. A total of 60 patients with cervical radicular pain due to a single-level disc herniation were randomized into either the FL or US group. The numeric rating scale, Short Form-36, and neck disability index were evaluated before treatment at months 1, 3, and 6 after treatment. Procedure time, complications, pain medication consumption, and patient satisfaction were also recorded. Patients experienced significant improvement in pain, disability, and quality of life scores up to 6 months after the procedure (p < 0.001). Treatment success rate was achieved in 56.6% of the IL-CESI group and 50% of the CSNRB group without any significant difference between the study arms (p = 0.617). US-guided CSNRB was shown to be as effective as the FL-guided IL-CESI in the treatment of cervical radicular pain, in addition to the absence of radiation exposure and requiring less procedure time.
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  • 文章类型: Journal Article
    三种新的单硫酸化聚羟基类固醇糖苷,香菇总皂苷A(1),B(2)、C(3)以及新的相关未硫酸化的单糖苷,香菇苷D(4),从在鄂霍次克海收集的海星Henricialeviusculaspiculifica的乙醇提取物中分离出来。化合物1-3含有两个碳水化合物部分,其中一个连接到类固醇四环核的C-3,而另一个位于苷元侧链的C-24。两个糖苷(2,3)是生物苷,和一个糖苷(1),不像他们,包括三个单糖残基。这种类型的三糖苷是一组罕见的海星极性类固醇。此外,首次在海星的类固醇糖苷中发现了5-取代的3-OSO3-α-L-Araf单元。细胞活力分析表明,1-3(浓度高达100μM)对人胚肾HEK293,黑色素瘤SK-MEL-28,乳腺癌MDA-MB-231和结肠直肠癌HCT116细胞的细胞毒性可忽略不计。这些化合物在无毒浓度下显着抑制HCT116细胞的增殖和集落形成,化合物3的效果最大。化合物3通过在G2/M期诱导剂量依赖性细胞周期停滞对HCT116细胞发挥抗增殖作用。调节细胞周期蛋白CDK2,CDK4,细胞周期蛋白D1,p21的表达和抑制蛋白激酶c-Raf的磷酸化,MEK1/2、ERK1/2的MAPK/ERK1/2通路。
    Three new monosulfated polyhydroxysteroid glycosides, spiculiferosides A (1), B (2), and C (3), along with new related unsulfated monoglycoside, spiculiferoside D (4), were isolated from an ethanolic extract of the starfish Henricia leviuscula spiculifera collected in the Sea of Okhotsk. Compounds 1-3 contain two carbohydrate moieties, one of which is attached to C-3 of the steroid tetracyclic core, whereas another is located at C-24 of the side chain of aglycon. Two glycosides (2, 3) are biosides, and one glycoside (1), unlike them, includes three monosaccharide residues. Such type triosides are a rare group of polar steroids of sea stars. In addition, the 5-substituted 3-OSO3-α-L-Araf unit was found in steroid glycosides from starfish for the first time. Cell viability analysis showed that 1-3 (at concentrations up to 100 μM) had negligible cytotoxicity against human embryonic kidney HEK293, melanoma SK-MEL-28, breast cancer MDA-MB-231, and colorectal carcinoma HCT 116 cells. These compounds significantly inhibited proliferation and colony formation in HCT 116 cells at non-toxic concentrations, with compound 3 having the greatest effect. Compound 3 exerted anti-proliferative effects on HCT 116 cells through the induction of dose-dependent cell cycle arrest at the G2/M phase, regulation of expression of cell cycle proteins CDK2, CDK4, cyclin D1, p21, and inhibition of phosphorylation of protein kinases c-Raf, MEK1/2, ERK1/2 of the MAPK/ERK1/2 pathway.
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