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Methyl jasmonate protects liver and pancreas tissues of adult diabetic rats from STZ-induced oxidative stress damage. 茉莉酸甲酯可保护成年糖尿病大鼠肝脏和胰腺组织免受stz诱导的氧化应激损伤。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-12 DOI: 10.1080/10286020.2025.2611910
Marjan Shabazi, Seifollah Bahramikia, Razieh Kooshki

This study evaluated the potential of methyl jasmonate (MeJA) to modulate oxidative stress damage and hyperglycemia in rats with STZ-induced diabetes. MeJA treatment (5 and 10 mg/kg) improved the destructive effects of STZ-induced oxidative damage, as proved by the decline in ROS formation and lipid peroxidation. In addition, MeJA displayed a substantial upsurge in the level of tissue GSH and activity of CAT and SOD enzymes. Histological analysis confirmed MeJA alleviated liver damage. Given the crucial part oxidative stress plays in the etiology of diabetes, this study offers a novel viewpoint on MeJA's potential as a treatment.

本研究评估茉莉酸甲酯(MeJA)对stz诱导的糖尿病大鼠氧化应激损伤和高血糖的调节潜力。MeJA处理(5和10 mg/kg)改善了stz诱导的氧化损伤的破坏作用,证明了ROS形成和脂质过氧化的下降。此外,MeJA在组织GSH水平和CAT和SOD酶活性方面表现出大幅上升。组织学分析证实MeJA减轻了肝损伤。鉴于氧化应激在糖尿病病因中起着至关重要的作用,本研究为MeJA作为一种治疗方法的潜力提供了一个新的观点。
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引用次数: 0
Research on the effects and mechanisms of the Yiqi Huoxue Recipe in improving renal injury in diabetic nephropathy through the HIF-1 pathway. 益气活血方通过HIF-1通路改善糖尿病肾病肾损伤的作用及机制研究
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-12 DOI: 10.1080/10286020.2025.2602695
Wen-Di Niu, Hao-Wei Liang, Lue Hong, Jin-Xing He, Jia-Hui Qian, Fei Pan, Zhi-Wei Xu, Hui Wang

This study investigates the therapeutic effects and mechanisms of the Yiqi Huoxue Recipe (YHR) on renal injury in Diabetic nephropathy (DN). Through mass spectrometry analysis, animal experiments, and network pharmacology approaches, it was found that YHR can ameliorate renal function indicators and pathological changes in DN rats, and reduce cell apoptosis. Mechanistic studies indicate that YHR alleviates hyperglycemia-induced renal inflammation and damage by inhibiting the HIF-1 signaling pathway, thereby improving DN.

本研究探讨益气活血方对糖尿病肾病(DN)肾损伤的治疗作用及其机制。通过质谱分析、动物实验、网络药理学等方法,发现YHR能改善DN大鼠肾功能指标和病理改变,减少细胞凋亡。机制研究表明,YHR通过抑制HIF-1信号通路减轻高血糖诱导的肾脏炎症和损伤,从而改善DN。
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引用次数: 0
Discovery of undescribed alkaloids with immunosuppressive activity from the endophytic fungus Penicillium sp. HZ-5. 内生真菌Penicillium sp. HZ-5中未描述的具有免疫抑制活性生物碱的发现。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-10 DOI: 10.1080/10286020.2025.2606379
Jie Li, Ye-Ting Zhang, Yusuf Abudula, Zhang-Rong Hou, Zheng-Yi Shi, Xin-Ye Huang, Ming Chen, Xue-Qi Lan, Ju-Bao Zhang, Chang-Xing Qi, Yong-Hui Zhang

Two undescribed alkaloids, mecichorine (1) and talaropyrazine D (2), along with four known compounds were isolated from an endophytic fungus Penicillium sp. HZ-5. Their structures were elucidated from the spectroscopic data. Furthermore, the isolated compounds were tested for their immunosuppressive activity, and compound 1 showed moderate immunosuppressive activity on Con A-induced T-lymphocyte proliferation in vitro, with an IC50 value of 15.2 ± 0.3 µM, and the others showed no obvious activities up to 40 µM.

从内生真菌青霉菌(Penicillium sp. HZ-5)中分离得到两种未描述的生物碱,mecichorine(1)和talaropyrazine D(2),以及四种已知化合物。通过光谱数据对它们的结构进行了分析。化合物1对Con a诱导的体外t淋巴细胞增殖具有中等的免疫抑制作用,IC50值为15.2±0.3µM,其余化合物在40µM以内无明显抑制作用。
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引用次数: 0
Two new iridoid glycosides from the roots of Dipsacus asper. 杨柏根中两个新的环烯醚萜苷。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-09 DOI: 10.1080/10286020.2025.2608810
Xin-Li Ma, Wan-Qi Zhang, Jing-Han Zhang, Gu Zhao, Xin-Yue Li, Ming-Hui Sun, Jie Zhou, Guo-Ru Shi, De-Quan Yu, Yan-Fei Liu

Two new iridoid glycosides, dasperosides A-B (1-2), together with two known analogues (3-4), were isolated from the air-dried roots of Dipsacus asper. Their structures were established from the spectroscopic data obtained and chemical evidence. Compounds 1-4 were tested for their cytotoxicity against six human tumor cell lines, hepatoprotective and anti-inflammatory activities.

从白杨(Dipsacus aspper)的风干根中分离到两个新的环烯醚萜苷类化合物dasperosides A-B(1-2)和两个已知的类似物(3-4)。根据获得的光谱数据和化学证据确定了它们的结构。化合物1 ~ 4对6种人类肿瘤细胞系的细胞毒性、肝保护和抗炎活性进行了测试。
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引用次数: 0
Synthesis and antibacterial activity of naringenin derivatives containing selenocyanate moiety. 含硒氰酸酯部分柚皮素衍生物的合成及抑菌活性研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-08 DOI: 10.1080/10286020.2025.2611908
Zhi-Ping Liu, Mai-Xia Liu, Chun-Rui Cai, Chun-Fang Gan, Jian-Guo Cui, Yan-Min Huang

To control plant pathogen infections, we synthesized naringenin derivatives bearing selenocyanate moieties and assayed their antibacterial activity against Xanthomonas axonopodis pv. citri, Xanthomonas oryzae pv. oryzae, and Xanthomonas oryzae pv. oryzicola via the microbroth dilution method. Structures were confirmed by 1H NMR, 13C NMR and HRMS. Compounds 4a and 4b featuring ether substitution at the 7-hydroxyl of naringenin showed potent activity against X. axonopodis pv. citri (EC50: 0.33-0.38 μg/ml) and X. oryzae pv. Oryzicola (EC50: 0.36-0.75 μg/ml), while 5b and 8c outperformed chlorothalonil against X. oryzae pv. Oryzae (EC50: 1.05-1.42 μg/ml). This study provides valuable insights for developing novel plant disease control agents.

为防治植物病原菌感染,合成了含硒氰酸酯的柚皮素衍生物,并测定了其对轴索黄单胞菌的抑菌活性。柑桔,米黄单胞菌;米黄单胞菌;通过微肉汤稀释法提取米霉。结构经1H NMR、13C NMR和HRMS确证。柚皮素7-羟基上醚取代的化合物4a和4b对轴足线虫具有较强的抗虫活性。柠檬酸橙(EC50: 0.33 ~ 0.38 μg/ml)和稻瘟病菌。5b和8c对稻瘟病病菌的EC50值为0.36 ~ 0.75 μg/ml,效果优于百菌清。Oryzae (EC50: 1.05 ~ 1.42 μg/ml)。该研究为开发新型植物病害防治剂提供了有价值的见解。
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引用次数: 0
Immunohistochemical and metabolomic analysis of Tibetan medicine triphala in response to pancreatic tissues of diabetic rats. 藏药三联对糖尿病大鼠胰腺组织的免疫组化和代谢组学分析。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-06 DOI: 10.1080/10286020.2025.2607494
Xue-Yan Li, Xiao-Mei Long, Tao Liu, Shuang Guo, Jian-Xing Gu, Fang-Fang Chen, Yi-Dan Fan, Hai-Peng Liu, Yuan Fan, Zhu-Sheng Tang

Tibetan Medicine Triphala (THL), consisting of Emblica officinalis, Terminalia bellerica, and Terminalia chebula, is a traditional Tibetan remedy for diabetes mellitus (DM). This study investigated THL's pancreatic metabolomic effects and impacts on paracrine factors (glucagon, insulin, somatostatin, pancreatic polypeptide) in diabetic rats. Rats were divided into six groups, gavaged for 8 weeks, with weekly blood glucose/body weight monitoring. THL reduced serum glucagon, somatostatin, pancreatic polypeptide, elevated insulin, restored pancreatic β-cell function, downregulated α/δ/pp cell expressions, normalized 5 key differential metabolites, and modulated four core metabolic pathways, exerting antidiabetic effects.

藏药三联戟(THL)是一种治疗糖尿病的传统藏药,由三联戟、三联戟和三联戟组成。本研究探讨THL对糖尿病大鼠胰腺代谢组学的影响及其对胰高血糖素、胰岛素、生长抑素、胰多肽等旁分泌因子的影响。将大鼠分为6组,灌胃8周,每周监测血糖/体重。THL降低血清胰高血糖素、生长抑素、胰多肽、胰岛素水平,恢复胰腺β细胞功能,下调α/δ/pp细胞表达,使5种关键差异代谢物正常化,调节4种核心代谢途径,具有降糖作用。
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引用次数: 0
New alkaloids from the twigs and leaves of tabernaemontana divaricata and their neuroprotective effects. 小红花嫩枝和叶中的新生物碱及其神经保护作用。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-06 DOI: 10.1080/10286020.2025.2608814
Dong-Hao Lu, Fei-Yan Wu, Nan Zhou, Xia Zhang, Zhen-Hua Li, Song Wang, Min Song, Zi-Wei Li, Xiao-Qi Zhang

Two novel monoterpenoid quinoline alkaloids, tabernacatines A and B (1 and 2), and a new monoterpenoid indole alkaloid, tabernacatine C (3), along with three known alkaloids (4 - 6), were isolated from the twigs and leaves of Tabernaemontana divaricata. Their structures were elucidated based on UV, IR, HR-ESI-MS, NMR spectra analysis, X-ray diffraction, and ECD calculation methods. Compounds 1 - 6 were evaluated for their neuroprotective effects in glutamate-induced HT22 cells, and compounds 4-6 exhibited potent neuroprotective effects.

从大葱的细枝和叶片中分离得到了两种新的单萜类喹啉生物碱,帐蓬碱A和B(1和2)和一种新的单萜类吲哚生物碱,帐蓬碱C(3),以及三种已知的生物碱(4 ~ 6)。通过UV、IR、HR-ESI-MS、NMR、x射线衍射、ECD计算等方法对其结构进行了鉴定。化合物1 ~ 6对谷氨酸诱导的HT22细胞具有神经保护作用,化合物4 ~ 6表现出较强的神经保护作用。
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引用次数: 0
Design and synthesis of a novel β-anhydroicartin derivative targeting tumor cell mitochondria based on the regulation of p16INK4a and its in vitro biological activity evaluation 基于p16INK4a调控的靶向肿瘤细胞线粒体的β-无氢蛋白衍生物的设计合成及其体外生物活性评价
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-02 DOI: 10.1080/10286020.2025.2488322
Hui Shu , Fang-Fei Liu , Feng-Yan Su , Qian Zhang , Yan Zhao , Wei Li , Jia-Hong Han , En-Bo Cai
Based on the regulation of β-anhydroicaritin on the stability of p16INK4a encoded by CDKN2A gene, nine novel triphenylphosphine derivatives targeting tumor cell mitochondria were synthesized. Compound 13 increased the ability to inhibit lung cancer A549 cells by 24 times compared with 5-fluorouracil. Biological studies have shown that compound 13 significantly promotes early apoptosis and induces mitochondrial dysfunction in A549 cells. Further studies showed that compound 13 arrested 73% of the cells in the G0/G1 phase, preventing the cells from entering the DNA synthesis phase. In summary, compound 13 is expected to be developed as a new targeted anti-tumor drug.
基于β-无氢牡丹花素对CDKN2A基因编码的p16INK4a稳定性的调控,合成了9种靶向肿瘤细胞线粒体的新型三苯基膦衍生物。化合物13对肺癌A549细胞的抑制能力是5-氟尿嘧啶的24倍。生物学研究表明,化合物13显著促进A549细胞早期凋亡,诱导线粒体功能障碍。进一步的研究表明,化合物13在G0/G1期阻滞了73%的细胞,阻止细胞进入DNA合成期。综上所述,化合物13有望成为一种新的靶向抗肿瘤药物。
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引用次数: 0
A network pharmacological target mendelian randomization study on the neuroprotective effects of active ingredients in mahuang fuzi xixin decoction for multiple sclerosis 麻黄附子西心汤有效成分对多发性硬化症神经保护作用的网络药理靶点孟德尔随机化研究。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-02 DOI: 10.1080/10286020.2025.2491612
Wei-Jie Li , Chong-Lian Feng , Zhao-Yuan Nie , Ling-Yun Li , Jian-Hui Guo , Xiang-Yu Liu , Yang-Hao Su , Shan-Shan Liu , Zhi-Zhong Cui
Mahuang Fuzi Xixin Decoction (MFX), a traditional Chinese medicine containing 44 volatile components (97.36% total oil), includes key compounds like α-terpenol (13.34%) and 1,2,3-trimethoxy-5-methyl-benzene (22.64%). Using network pharmacology and Mendelian randomization, 24 active compounds were identified targeting MS-related pathways (NF-κB, NLRP3, Toll-like receptor). Genetic variants in CYP450, GSK3B, CYBB, and PON1 correlated with reduced MS risk. In EAE mice, MFX decreased spinal GSK-3B expression (immunofluorescence) and pro-inflammatory factors (ELISA), demonstrating neuroprotection via anti-inflammatory, antioxidative mechanisms and restored GSK-3B levels, highlighting therapeutic potential for MS.
中药麻黄附子西心汤含有44种挥发性成分(占总油的97.36%),主要成分为α-萜酚(13.34%)和1,2,3-三甲氧基-5-甲基苯(22.64%)。采用网络药理学和孟德尔随机化方法,鉴定出24种靶向ms相关通路(NF-κB、NLRP3、toll样受体)的活性化合物。CYP450、GSK3B、CYBB和PON1基因变异与MS风险降低相关。在EAE小鼠中,MFX降低脊髓GSK-3B表达(免疫荧光)和促炎因子(ELISA),通过抗炎、抗氧化机制显示神经保护作用,并恢复GSK-3B水平,突出了MS的治疗潜力。
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引用次数: 0
Advances in drug design strategies for phototherapy based on tumor cell death mechanisms 基于肿瘤细胞死亡机制的光疗药物设计策略研究进展。
IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Pub Date : 2026-01-02 DOI: 10.1080/10286020.2025.2530748
Zheng-Hao Chen , Xin-De Li , Mei-Zhen Luo , Wu-Yu Mao , Shuai Huang , Xian-Li Zhou
Photodynamic therapy (PDT) is a promising non-invasive tumor treatment. Researchers study cell death mechanisms—apoptosis, necrosis, and autophagy—to improve photosensitizer design for precise tumor destruction while sparing normal tissue. This review summarizes these biological causes of cell death. It focuses on recent innovations in PDT drug development and therapeutic techniques, specifically detailing how photosensitizers kill cancer cells. The paper also highlights clinical challenges faced by therapies targeting these common mechanisms and the potential of novel mechanisms. It aims to provide new perspectives on tumor death mechanisms and PDT drug development, offering a basis for novel smart PDT systems.
光动力疗法(PDT)是一种很有前途的非侵入性肿瘤治疗方法。研究人员研究细胞死亡机制——凋亡、坏死和自噬——以改进光敏剂的设计,以精确地破坏肿瘤,同时保留正常组织。本文综述了细胞死亡的生物学原因。它侧重于PDT药物开发和治疗技术的最新创新,特别是详细介绍了光敏剂如何杀死癌细胞。本文还强调了针对这些常见机制的治疗所面临的临床挑战和新机制的潜力。旨在为肿瘤死亡机制和PDT药物开发提供新的视角,为新型智能PDT系统提供基础。
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引用次数: 0
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Journal of Asian Natural Products Research
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