Lei Song
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Lei Song has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
Chang Ren
Southwest Minzu University
2 shared publicationsJun Gu
Sichuan University West China Hospital: West China Hospital of Sichuan University
2 shared publications- Xiaoling Wang
College of Pharmacy and Food, Southwest Minzu University, Chengdu 610041, China
2 shared publications - Bang-Jing Li
Key Laboratory of Mountain Ecological Restoration and Bioresource Utilization, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, Sichuan, China
1 shared publication - Chang Ren
College of Pharmacy and Food Southwest Minzu University Chengdu Sichuan China
1 shared publication - Cheng-Yuan Xing
College of Pharmacy, Southwest Minzu University, Chengdu 610041, China
1 shared publication
Latest Publications
- Open Access
- 27 January 2026
- Published by Brieflands in Jundishapur Journal of Natural Pharmaceutical Products
- Vol. 21 (1) , e168126
Erratum: Allicin Alleviates Aortic Dissection Progression via p38/MAPK/NF-κB Signaling Pathways [Jundishapur J Nat Pharm Prod. 2025; 20 (4): e165405]
This corrects the article Allicin Alleviates Aortic Dissection Progression via p38/MAPK/NF-κB Signaling Pathways. Dear Readers, Following the publication of the above-mentioned article, an error was identified in the authors' names (1). In the published version, the authors' names were incorrectly listed as "Wuyi wu Ban" and "Liying wu Qiu." The correct author names are as follows:-Wuyi Ban-Liying Qiu These corrections pertain only to the authorship information and do not affect the scientific content, results, or conclusions of the article.
- 27 January 2026
- Published by Brieflands in Jundishapur Journal of Natural Pharmaceutical Products
- Vol. 21 (1) , e168126
Open AccessErratum: Allicin Alleviates Aortic Dissection Progression via p38/MAPK/NF-κB Signaling Pathways [Jundishapur J Nat Pharm Prod. 2025; 20 (4): e165405]
This corrects the article Allicin Alleviates Aortic Dissection Progression via p38/MAPK/NF-κB Signaling Pathways. Dear Readers, Following the publication of the above-mentioned article, an error was identified in the authors' names (1). In the published version, the authors' names were incorrectly listed as "Wuyi wu Ban" and "Liying wu Qiu." The correct author names are as follows:-Wuyi Ban-Liying Qiu These corrections pertain only to the authorship information and do not affect the scientific content, results, or conclusions of the article.
- Open Access
- 24 October 2024
- Published by Springer Nature in Research Square
Berberine prevents the formation of aortic dissection in C57BL/6 mice through the regulation of vascular smooth muscle cell function
Purpose Aortic dissection (AD) represents a critical medical condition characterized by a high mortality rate and limited therapeutic options. The pathogenesis of AD is associated with the extracellular matrix degradation, phenotypic switching and the loss of vascular smooth muscle cells (VSMCs). Berberine (BBR) has demonstrated promising protective effects in various cardiovascular diseases, but its impact on AD and the underlying mechanisms remains unexplored. This study aims to investigate the potential of BBR in reducing the development of AD and preventing the phenotypic transformation of VSMCs, thereby proposing a novel therapeutic strategy for this life-threatening condition. Methods C57BL/6J mice and isolated VSMCs were used as in vivo and in vitro models, respectively. An AD mouse model was established through intragastric administration of β-aminopropionitrile monofumarate (BAPN), and VSMC phenotypic transformation was induced by angiotensin II (Ang-II) to assess the preventative effects of BBR. Results BBR significantly mitigates AD in a BAPN-induced mouse model by reducing AD incidence from 80–45% and increasing survival rates from 50–70%. BBR treatment alleviates aortic dilation and improves aortic morphology, while also attenuating extracellular matrix degradation, as evidenced by reduced collagen type I and fibronectin degradation. Histological and immunohistochemical analyses reveal that BBR diminishes inflammation, as indicated by reduced IL-6 and HIF-1α expression, and mitigates oxidative stress by lowering MDA levels and enhancing SOD activity. Additionally, BBR counteracts VSMC phenotypic transformation and apoptosis, demonstrated by restored contractile protein levels and reduced caspase-3, AKT, and PI3K levels. It also inhibits VSMC proliferation, migration, and MMP expression in vitro, highlighting its protective role against AD progression. Conclusion BBR exhibits protective effects against BAPN-induced AD in C57BL/6J mice, highlighting its potential as a viable and innovative therapeutic option for preventing AD progression.
- 24 October 2024
- Published by Springer Nature in Research Square
Open AccessBerberine prevents the formation of aortic dissection in C57BL/6 mice through the regulation of vascular smooth muscle cell function
Purpose Aortic dissection (AD) represents a critical medical condition characterized by a high mortality rate and limited therapeutic options. The pathogenesis of AD is associated with the extracellular matrix degradation, phenotypic switching and the loss of vascular smooth muscle cells (VSMCs). Berberine (BBR) has demonstrated promising protective effects in various cardiovascular diseases, but its impact on AD and the underlying mechanisms remains unexplored. This study aims to investigate the potential of BBR in reducing the development of AD and preventing the phenotypic transformation of VSMCs, thereby proposing a novel therapeutic strategy for this life-threatening condition. Methods C57BL/6J mice and isolated VSMCs were used as in vivo and in vitro models, respectively. An AD mouse model was established through intragastric administration of β-aminopropionitrile monofumarate (BAPN), and VSMC phenotypic transformation was induced by angiotensin II (Ang-II) to assess the preventative effects of BBR. Results BBR significantly mitigates AD in a BAPN-induced mouse model by reducing AD incidence from 80–45% and increasing survival rates from 50–70%. BBR treatment alleviates aortic dilation and improves aortic morphology, while also attenuating extracellular matrix degradation, as evidenced by reduced collagen type I and fibronectin degradation. Histological and immunohistochemical analyses reveal that BBR diminishes inflammation, as indicated by reduced IL-6 and HIF-1α expression, and mitigates oxidative stress by lowering MDA levels and enhancing SOD activity. Additionally, BBR counteracts VSMC phenotypic transformation and apoptosis, demonstrated by restored contractile protein levels and reduced caspase-3, AKT, and PI3K levels. It also inhibits VSMC proliferation, migration, and MMP expression in vitro, highlighting its protective role against AD progression. Conclusion BBR exhibits protective effects against BAPN-induced AD in C57BL/6J mice, highlighting its potential as a viable and innovative therapeutic option for preventing AD progression.
- Open Access
- 2 October 2024
- Published by Elsevier in Asian Journal of Surgery
- Vol. 48 (3) , 2074-2075
Procyanidin prevents aortic dissection by inhibiting phenotypic switch of vascular smooth muscle cells
- 2 October 2024
- Published by Elsevier in Asian Journal of Surgery
- Vol. 48 (3) , 2074-2075
Open AccessProcyanidin prevents aortic dissection by inhibiting phenotypic switch of vascular smooth muscle cells
- Open Access
Recent Progress in Synthesis of Alkyl Fluorinated Compounds with Multiple Contiguous Stereogenic Centers
Organic fluorides are widely used in pharmaceuticals, agrochemicals, material sciences, and other fields due to the special physical and chemical properties of fluorine atoms. The synthesis of alkyl fluorinated compounds bearing multiple contiguous stereogenic centers is the most challenging research area in synthetic chemistry and has received extensive attention from chemists. This review summarized the important research progress in the field over the past decade, including asymmetric electrophilic fluorination and the asymmetric elaboration of fluorinated substrates (such as allylic alkylation reactions, hydrofunctionalization reactions, Mannich addition reactions, Michael addition reactions, aldol addition reactions, and miscellaneous reactions), with an emphasis on synthetic methodologies, substrate scopes, and reaction mechanisms.
Open AccessRecent Progress in Synthesis of Alkyl Fluorinated Compounds with Multiple Contiguous Stereogenic Centers
Organic fluorides are widely used in pharmaceuticals, agrochemicals, material sciences, and other fields due to the special physical and chemical properties of fluorine atoms. The synthesis of alkyl fluorinated compounds bearing multiple contiguous stereogenic centers is the most challenging research area in synthetic chemistry and has received extensive attention from chemists. This review summarized the important research progress in the field over the past decade, including asymmetric electrophilic fluorination and the asymmetric elaboration of fluorinated substrates (such as allylic alkylation reactions, hydrofunctionalization reactions, Mannich addition reactions, Michael addition reactions, aldol addition reactions, and miscellaneous reactions), with an emphasis on synthetic methodologies, substrate scopes, and reaction mechanisms.
- Open Access
β-Cyclodextrin-Based Poly (Vinyl Alcohol) Fibers for Sustained Release of Fragrances
Poly (vinyl alcohol)/β-cyclodextrin (PVA/CD) composite fibers are prepared by wet spinning followed by hot stretching. XRD results show that β-CDs are in an amorphous state in fiber, and β-CD can help maintain the fibrous crystal that exists in the composite fiber. The DSC results show that the total crystalline ratio of the composite fibers decreased with the increase of β-CD. The as-prepared composite fibers were further crosslinked with glutaraldehyde (GA) to improve their usability. The crosslinked structure, together with amorphous β-CD, contributes to the loading and sustained release of fragrance molecules that were studied. The fragrance retention ratio of PVA/CD/GA is 55.63% and 48.25% for cis-jasmone and citronella, even after 25 days. The inclusion complexes of β-CD and fragrance molecules are confirmed by 2D-FTIR, which is responsible for the sustained release of fragrance. This study may contribute to the mass production of wearable long-term scented fabrics.
Open Accessβ-Cyclodextrin-Based Poly (Vinyl Alcohol) Fibers for Sustained Release of Fragrances
Poly (vinyl alcohol)/β-cyclodextrin (PVA/CD) composite fibers are prepared by wet spinning followed by hot stretching. XRD results show that β-CDs are in an amorphous state in fiber, and β-CD can help maintain the fibrous crystal that exists in the composite fiber. The DSC results show that the total crystalline ratio of the composite fibers decreased with the increase of β-CD. The as-prepared composite fibers were further crosslinked with glutaraldehyde (GA) to improve their usability. The crosslinked structure, together with amorphous β-CD, contributes to the loading and sustained release of fragrance molecules that were studied. The fragrance retention ratio of PVA/CD/GA is 55.63% and 48.25% for cis-jasmone and citronella, even after 25 days. The inclusion complexes of β-CD and fragrance molecules are confirmed by 2D-FTIR, which is responsible for the sustained release of fragrance. This study may contribute to the mass production of wearable long-term scented fabrics.