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sumatriptan succinate (Imigran Nasal Spray / Imitrex Nasal Spray / Suminant)

✓ Approved

GSK · HTR1D · 小分子

什么是 sumatriptan succinate?

sumatriptan succinate 是一种小分子,由GSK研发。该药已获批,用于治疗相关适应症,给药途径:Inhaled。

药物档案

商品名Imigran Nasal Spray, Imitrex Nasal Spray, Suminant
公司GSK
药物类别小分子
分子靶点HTR1D
给药途径Inhaled
状态Approved

作用机制

分子靶点

sumatriptan succinate 作用于 1 个分子靶点:

HTR1D5-hydroxytryptamine receptor 1D (HTR1DA, HT1DA)
需要更深入的分析?Noah AI 可解释复杂机制并与同类药物比较。

治疗适应症

sumatriptan succinate 针对 2 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Nervous system disordersMigraine✓ Approved
Nervous system disordersCluster headache✓ Approved

相关研究文献

PubMedZhonghua yu fang yi xue za zhi [Chinese journal of preventive medicine]2026-07-27

[Research progress of gut microbial metabolite succinate in inflammatory diseases].

Chen Y X YX, Niu M M, Du Y Y

Inflammatory diseases are pathological conditions precipitated by inflammation, with the gut microbiota and its metabolites playing a pivotal role in the inflammatory process. Succinate, a key metabolite generated by gut microorganisms, is implicated not only in the energy metabolism of the tricarboxylic acid cycle but also in the modulation of inflammatory processes via the succinate receptor 1-mediated immune regulatory pathway. This review provides a unified elaboration on the metabolic pathways and biological characteristics of succinate, the detection techniques for succinate, and the potential applications of succinate in the diagnosis and treatment of inflammatory diseases, aiming to provide a scientific basis for the development of relevant diagnosis and treatment strategies.

PMID 42503938
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PubMedMolecular pharmaceutics2026-07-27

Correction to "d-α-Tocopherol Polyethylene Glycol Succinate-Based Redox-Sensitive Paclitaxel Prodrug for Overcoming Multidrug Resistance in Cancer Cells".

Bao Yuling Y, Guo Yuanyuan Y, Zhuang Xiangting X, Li Dan D et al.

PMID 42505427
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PubMedAnatomia, histologia, embryologia2026-07-27

Computed Tomographic Volumetric Analysis of the Nasal Cavities in Domestic Cats (Felis catus) and Anatomical Implications for Intranasal Drug Delivery.

Charles Montel M, Hippolyte Charlier C, Charlène Paquet P, Géraldine Jourdan J et al.

To perform a computed tomography (CT)-based volumetric assessment of the nasal cavities in domestic cats and to evaluate the relationship between nasal cavity volume and selected morphometric variables. Fifty-six European cats that underwent CT examination of the head were retrospectively included. Three-dimensional segmentation of the right and left nasal cavities was performed using dedicated software. Total, right, and left nasal cavity volumes were measured. Associations between nasal cavity volume and sex, age, and body weight were assessed using multiple linear regression analysis. Bilateral symmetry was evaluated using paired comparisons. Intra-observer reliability was determined using the intraclass correlation coefficient (ICC). Mean total nasal cavity volume was 6.74 ± 1.79 mL. No significant difference was observed between left (3.38 ± 0.92 mL) and right (3.36 ± 0.91 mL) nasal cavity volumes. Male cats exhibited significantly larger nasal cavity volumes than females (8.3 ± 1.7 mL vs. 5.8 ± 1.1 mL; p < 0.001). No significant association was found between nasal cavity volume and age or body weight after adjustment for sex. Intra-observer agreement was excellent (ICC = 0.98). CT-based three-dimensional segmentation provides reliable volumetric assessment of the feline nasal cavities. Significant sexual dimorphism was identified, whereas laterality, age, and body weight had no significant influence on nasal cavity volume. The limited nasal cavity volume supports the use of low-volume, concentrated formulations for intranasal drug delivery in cats.

PMID 42504038
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PubMedMicroscopy and microanalysis : the official journal of Microscopy Society of America, Microbeam Analysis Society, Microscopical Society of Canada2026-07-27

Comparative Histological Architecture of the Nasal Skin in Domestic Animals: Structural Insights into Species-Specific Adaptations.

Madkour Fatma A FA, Mohammed Elsayed S I ESI

The nasal skin in domestic animals plays a crucial role in thermoregulation, tactile perception, and environmental interaction. This study aimed to compare the histological architecture of the nasal skin among common domestic species to identify species-specific morphological variations. Nasal skin samples from camel, buffalo, cattle, sheep, goat, horse, donkey, pig, and dog were collected and processed for histological investigation. The epidermis was thickest in buffalo and thinnest in camel, exhibiting a wavy surface in camel, donkey, and dog. Epithelial pegs and dermal papillae were well developed in ruminants but sparse or absent in camel and horse. The dermis contained hair follicles, sebaceous glands, and sweat glands, although their presence varied among species. Hair follicles and sebaceous glands were absent in the modified nasal skin, except in pig and sheep. Sweat glands were few in camel, buffalo, cattle, horse, donkey, and sheep, but absent in other species. Nasal glands were well-developed in buffalo and cattle, but absent in camel and dog. Skeletal muscle bundles were prominent in the dermis of the horse's nasal skin, particularly within the reticular layer. The presence of marked interspecies variations in domestic animal's nasal skin histology indicates structural and functional adaptations.

PMID 42504865
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PubMedMetabolites2026-07-27

Integrated Multi-Omics Links Bisphenol AF (BPAF) Exposure to Hepatic Lipid Metabolism Disruption via Succinate Dehydrogenase Dysfunction and Mitochondrial Impairment.

Wang Ning N, Xu Jing J, Leng Jing J, Xu Jia-Le JL et al.

Background/Objective: Bisphenol AF (BPAF), a fluorinated analogue of bisphenol A, is an environmental contaminant associated with hepatotoxicity and metabolic disruption. However, the systematic molecular mechanisms linking early transcriptional events to metabolic dysfunction in the liver remain poorly defined. The aim of this study is to elucidate the association between BPAF exposure and hepatic lipid accumulation by integrating transcriptomics, cellular metabolomics, and targeted phenotypic assays. Methods: We performed RNA-sequencing on livers from mice exposed to BPAF (0.1-10 mg/kg/day, 28 days), and performed non-targeted metabolomics on AML12 murine hepatocytes co-cultured with RAW264.7 macrophages in a Transwell system (0-2500 nM BPAF, 48 h). Key metabolic pathways were identified through integrated bioinformatics and validated using enzymatic assays, qRT-PCR, Western blotting, and phenotypic staining (lipid droplets, ROS). Results: Multi-omics integration revealed significant disruption of PPAR signaling and the tricarboxylic acid (TCA) cycle. A striking dose-dependent accumulation of succinate was observed in exposed cells, concomitant with a significant inhibition of succinate dehydrogenase (SDH) activity (52% reduction at 2500 nM, p < 0.001). Transcriptomic data confirmed the downregulation of mitochondrial fatty acid β-oxidation genes. Phenotypic validation indicated that BPAF exposure is associated with oxidative stress, pro-inflammatory cytokine release (TNF-α, IL-6), and pronounced intracellular lipid droplet accumulation in hepatocytes. Conclusions: This study suggests that BPAF exposure is associated with SDH dysfunction, TCA cycle arrest, and lipid dysregulation. Whether BPAF directly inhibits SDH or acts through upstream mitochondrial targets warrants further structural and kinetic investigation.

PMID 42506394
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PubMedEuropean archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery2026-07-27

Systematic review of non-surgical etiologies of nasal necrosis: evidence from case reports and case series.

Chedid Marie Line ML, Hariri Rima Mohammad Achraf RMA, Chaer Talia El TE, Murillo Veronica Andrade VA et al.

Nasal necrosis is a rare but potentially devastating manifestation of diverse conditions, including fulminant infection, immune-mediated vasculopathy, drug toxicity, neoplasia and device-related pressure injury. Surgical intervention is often prioritized; however, a subset of patients is managed non-surgically and evidence-based guidance remains limited. The objective is to systematically synthesize non-surgical etiologies, clinical patterns, diagnostic workup, and management strategies reported in cases of nasal necrosis. A systematic search of PubMed, Scopus and ScienceDirect from inception to December 7, 2025 identified case reports and case series involving human patients with nasal skin or soft-tissue necrosis not primarily attributable to surgery or cosmetic procedures. Non-human studies, systematic reviews and non english records were excluded. Data on demographics, etiology, presentation, investigations, management and outcomes were extracted. Methodological quality was appraised using Joanna Briggs Institute (JBI) tools. Thirty-nine publications comprising 45 cases were included. Infectious etiologies were most frequent (44.4%), followed by mechanical or traumatic (20.0%), immune-mediated (13.3%), drug-induced (13.3%), neoplastic (6.7%), and congenital causes (2.2%). Isolated nasal involvement occurred in 57.8% of cases. Non-surgical management included antimicrobials, corticosteroids, immunosuppressive agents, anticoagulation, wound care, and adjunctive hyperbaric oxygen therapy, with better outcomes in cases where the underlying cause was identified early. Nasal necrosis represents a heterogeneous clinicopathologic endpoint in which prompt etiologic diagnosis is critical for effective, organ-preserving dermatologic management.

PMID 42507212
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