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sumatriptan succinate (Zelrix / NP101 / Zecuity)

✓ Approved

Nupathe Inc. · HTR1D · 小分子

什么是 sumatriptan succinate?

sumatriptan succinate 是一种小分子,由Nupathe Inc.研发。该药已获批,用于治疗相关适应症,给药途径:Topical、Transdermal。

药物档案

商品名Zelrix, NP101, Zecuity
公司Nupathe Inc.
药物类别小分子
分子靶点HTR1D
给药途径Topical, Transdermal
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 1 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

相关研究文献

PubMedEuropean journal of endocrinology2026-08-04

Pharmacokinetics of inhaled prednisolone for adrenal crisis: an exploratory study.

Berends Julia M E JME, Vulto Annet A, van den Wijngaard Pascalle A PA, Vos Michel J MJ et al.

An adrenal crisis is a potentially life-threatening medical emergency, which requires rapid treatment with glucocorticoids. Guidelines advise immediate self-administration of hydrocortisone by intramuscular injection using an emergency management kit in case an adrenal crisis is suspected. However, self-injection is often not performed due to administration complexity or patient anxiety. Pulmonary administration of glucocorticoids may be a more patient-friendly and suitable alternative, especially when administered using a dry powder inhaler. Before advancing to the development of a dry powder inhaler, we aimed to evaluate whether the pharmacokinetics of inhaled prednisolone sodium succinate are suitable for the outpatient treatment of adrenal crisis. Twelve healthy participants (aged 23-31 years, 50% females) received two separate doses of prednisolone sodium succinate, equivalent to 56.1 and 112.2 mg prednisolone on separate occasions, administered via a nebulizer. The primary outcome was the time to reach a target plasma concentration of 200 nmol/L. The median times to achieve this plasma concentration (excluding the nebulization time of approximately 10 minutes) were 17 (13 - 23) minutes and 9 (5-11) minutes for the 56.1 and 112.2 mg doses, respectively. Furthermore, pulmonary administered prednisolone sodium succinate was well tolerated. The results of this study, particularly the short time to the target plasma concentration, indicate that prednisolone sodium succinate is rapidly absorbed via the lungs and that the pharmacokinetics of inhaled nebulized prednisolone sodium succinate are suitable for the outpatient treatment of adrenal crisis.

PMID 42549826
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PubMedJournal of bioenergetics and biomembranes2026-08-04

Correction: Succinate and lactate produced as conserved biomarkers through chronic and transient substrate-level phosphorylation: from microorganisms to cancer.

Lee Derek C DC, Duraj Tomas T, Chinopoulos Christos C, Seyfried Thomas N TN

PMID 42550324
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PubMedPediatric blood & cancer2026-08-03

Clinical Heterogeneity and Long-Term Outcomes of Pediatric Gastrointestinal Stromal Tumors: A Series of Four Patients Highlighting SDH-Deficient and SDH-Intact Subtypes.

Elfarraj Hala H, Barbar Maha M, Sultan Iyad I, Halalsheh Hadeel H

Pediatric gastrointestinal stromal tumors (GISTs) are rare, often lacking KIT or platelet-derived growth factor receptor-alpha (PDGFRA) mutations and driven by succinate dehydrogenase (SDH) deficiency. We report four pediatric patients (three females and one male) managed over a 19-year period. Two female patients had SDH-deficient tumors; one suffered metastatic relapse, illustrating the recurrent clinical course of this subtype. Of the two remaining cases, one SDH-intact female remains in remission 8 years post-diagnosis. The male patient demonstrated imatinib resistance but responded to sunitinib, facilitating gastrectomy. Despite a local recurrence managed by secondary wedge resection, he remains in remission. Comprehensive molecular profiling is essential for navigating GIST's clinical heterogeneity.

PMID 42544736
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PubMedPhysiologia plantarum2026-08-03

Physiological, Transcriptional, and Metabolic Variations During Dormancy Release Across Potato Cultivars Revealed by Integrated Multi-Omics Analysis.

Tian Shuaibing S, Wei Guocheng G, Zhu Xia X, Wang Xiyao X et al.

Tuber dormancy length is a key agronomic trait determining potato storage quality and planting suitability, yet the underlying molecular regulatory mechanisms remain poorly understood. In this study, we perform a time-course physiological, transcriptomic, and metabolomic analysis of a long-dormancy cultivar 'Chuanliangshu 10' and a short-dormancy cultivar 'Favorita' at harvest and storage. The short-dormancy cultivar 'Favorita' exhibits a significantly faster conversion rate of starch to soluble sugars during storage compared to 'Chuanliangshu 10'. Integrated transcriptomic and metabolomic analyses revealed that 'Favorita' likely accelerates dormancy release and sprouting through the coordinated regulation of multiple metabolic pathways. First, the expression of S-adenosyl-L-homocysteine hydrolase genes (SAHH1/2) in the cysteine and methionine metabolism pathway is significantly up-regulated, accompanied by a marked accumulation of the key metabolite glutathione (GSH). Second, the phenylalanine ammonia-lyase gene (PAL) is continuously and strongly up-regulated during dormancy release, coinciding with the accumulation of the intermediate metabolites fumarate and succinate of the phenylalanine metabolism pathway. Third, expression of the zeatin-deactivating gene CKX is strongly suppressed, resulting in zeatin accumulation and thereby promoting tuber sprouting. Last but not least, the pentose phosphate pathway genes including PGD, RPIA and TKTA are significantly upregulated during storage, indicating activation of this pathway. Collectively, this study systematically elucidates the physiological, transcriptomic, and metabolomic differences between potato cultivars with contrasting dormancy characteristics, providing a theoretical foundation and candidate gene resources for precisely regulating tuber dormancy and improving potato storage traits.

PMID 42543838
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PubMedZhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica2026-08-03

[Study on mechanism of Zhenwu Decoction against heart-kidney Yang deficiency-induced heart failure via cAMP/PKA signaling pathway].

Li Ya-Shu YS, Zhao Jing J, Li Jian-Bei JB, Zhang Xin-Ting XT et al.

This study aimed to investigate the effects of Zhenwu Decoction(ZWT) on cardiac fibrosis in mice with heart-kidney Yang deficiency-induced chronic heart failure(CHF). The research further explored the therapeutic mechanisms of ZWT in CHF treatment in the hope of providing novel insights for TCM approaches to managing heart-kidney Yang deficiency-induced heart failure. Sixty C57BL/6 mice were randomly divided into the following groups: the control group(normal untreated mice),the DOX group(doxorubicin-induced CHF model),the low-dose ZWT group(ZWT-L,4.7 g·kg~(-1)),the medium-dose ZWT group(ZWT-M,9.3 g·kg~(-1)),the high-dose ZWT group(ZWT-H,18.6 g·kg~(-1)),and the dopamine group(DA,positive control). The CHF mouse model was established over a 4-week period, which was followed by an additional 4-week treatment regimen. After 8 weeks, the spontaneous locomotor activity of mice was assessed, and TCM syndrome scoring was performed. Mouse serum samples were collected and analyzed to measure the levels of cardiac-specific biomarkers including cardiac troponin Ⅰ(cTn-Ⅰ),brain natriuretic peptide(BNP), creatine kinase-MB isoenzyme(CK-MB), creatine kinase(CK),lactate dehydrogenase(LDH),triiodothyronine(T3),succinate dehydrogenase(SDH) and myocardial cyclic adenosine monophosphate(cAMP). Cardiac tissue was collected for pathological examination. Western blot and real-time quantitative polymerase chain reaction(RT-PCR) were used to detect the expression of myocardial cAMP-dependent protein kinase catalytic subunit(PKA C),protein kinase A(PKA),ryanodine receptor 2(RyR2),phospholamban(PLB),B-cell lymphoma-2(Bcl-2),caspase-3,cleaved caspase-3 and Bcl-2-associated X protein(Bax). The experimental results indicated that, compared with the control group, the DOX group exhibited significantly elevated TCM syndrome scores accompanied by decreased heart rate, reduced body weight, and increased cardiac index(P<0.05); serum levels of CK, CK-MB, BNP, cTn-Ⅰ, LDH and myocardial cAMP were significantly increased(P<0.05), while SDH and T3 levels were decreased(P<0.05); meanwhile, myocardial interstitial fibrosis was aggravated and myocardial hypertrophy appeared; the expression of PKA C, PKA, caspase-3, cleaved caspase-3, Bax and phosphorylation of RyR2 were increased(P<0.05), the expression of Bcl-2 and phosphorylation of PLB were decreased compared with the DOX group, the ZWT treated groups demonstrated reduced TCM syndrome scores, increased heart rate, improved body weight, and decreased cardiac index. Additionally, serum levels of CK, CK-MB, BNP, cTn-Ⅰ, LDH and myocardial cAMP were decreased(P<0.05), while SDH and T3 levels were increased(P<0.05); myocardial hypertrophy and fibrosis were also improved; the expression of PKA C, PKA, Bax, caspase-3, cleaved caspase-3 and phosphorylation of RyR2 was reduced(P<0.05), and the expression of Bcl-2 and phosphorylation of PLB were increased(P<0.05). These findings suggested that ZWT may exert therapeutic effects on CHF by regulating sarcoplasmic reticulum calcium-related proteins, reducing apoptosis, and improving cardiac function.

PMID 42543375
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PubMedJournal of physiology and biochemistry2026-08-02

Circulating succinate changes during acute cold exposure are not related with brown adipose tissue in humans.

Osuna-Prieto Francisco J FJ, Martinez-Tellez Borja B, Sánchez-Delgado Guillermo G, Acosta Francisco M FM et al.

Brown adipose tissue (BAT) activity in humans is linked to better glucose metabolism and cardiometabolic health. In mice, cold exposure increases circulating succinate and enhances BAT thermogenesis, but whether similar succinate responses occur in humans remains undetermined. We analysed data from 33 young (18-25 years), sedentary adults (20 women) from the ACTIBATE cohort (NCT02365129). Plasma succinate was measured enzymatically at baseline and 60 and 120 min during a personalized cooling protocol. BAT volume, activity, and radiodensity were assessed via static 18F-fluorodeoxyglucose positron emission tomography-computed tomography (18F-FDG PET-CT) at the end of the cold exposure. Circulating succinate changed over time during cold exposure, with no significant change at 60 min and a significant increase at 120 min versus baseline (+ 23.8%, P = 0.017), with substantial interindividual variability. Exploratory stratification by median baseline succinate revealed divergent temporal patterns: the low-baseline group showed increases at 60 min (+ 46%) and 120 min (+ 80.5%; both P ≤ 0.021), while the high-baseline group showed reductions at both timepoints (-31.4% and - 2.4%; both P ≤ 0.003). These profiles were not explained by phenotypic or BAT-related parameters. In the full cohort, changes in circulating succinate were not associated with BAT outcomes. Overall, our findings indicate that circulating succinate responses during acute cold exposure are highly heterogeneous and no associated with BAT PET/CT-derived parameters in humans.

PMID 42541662
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