收藏切换
Monosialotetrahexosylganglioside protects brain injury in neonatal rats based on the UCH-L1/BDNF pathway
收藏切换
PDF
Er-qing XING1a, Yu ZHANG1b, Jia-xing SHANG1c, Cheng-xiang WANG1a, Sui-liang XIE1a, Xiang-hua WANG1a, Wen-ting DOU1a
Chinese Journal of Clinical Pharmacology | 2025, 41(4) : 512 - 516
Less
收藏切换
Chinese Journal of Clinical Pharmacology | 2025, 41(4): 512-516
Clinical and Basic Bridging Research
Monosialotetrahexosylganglioside protects brain injury in neonatal rats based on the UCH-L1/BDNF pathway
Full
Er-qing XING1a, Yu ZHANG1b, Jia-xing SHANG1c, Cheng-xiang WANG1a, Sui-liang XIE1a, Xiang-hua WANG1a, Wen-ting DOU1a
Affiliations
  • 1a.Pediatric Ward 1, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
  • 1b.Pediatrics, Neonatology Eastern, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
  • 1c.Cardiovascular Medicine, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
Published: 2025-02-28 doi: 10.13699/j.cnki.1001-6821.2025.04.013
Outline
收藏切换
Objective

To investigate the protective effects of monosialotetrahexosylganglioside (GM1) on hypoxic-ischemic brain damage (HIBD) in neonatal rats based on the ubiquitin C-terminal hydrolase L1 (UCH-L1)/brain-derived neurotrophic factor (BDNF) signaling pathway.

Methods

Twenty-day-old SD rats were randomly divided into model group, sham group and experimental group, with 10 rats in each group. Rats in model group and experimental group were lapped with left common carotid artery and placed in anoxic chamber with a certain oxygen to nitrogen ratio (8∶92) for 2 h to construct HIBD model. After the successful construction of the model, the experimental group was intraperitoneally injected with 20 mg·kg-1·d-1GM1, and the model group and sham group were injected with 0.9 % NaCl (0.25 mL·kg-1). The modified neurological severity score (mNSS) was used to evaluate the degree of neurological damage in the treated rats. Cerebral infarction was detected by 2,3,5-triphenyte-trazoliumchloride staining method; cerebral water content was determined by wet and dry weight method; cognitive ability was assessed by Morris water maze test; apoptosis was detected by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling; inflammatory factors were detected by enzyme-linked immunosorbent assay; UCH-L1 and BDNF protein levels were detected by Western blot.

Results

After different treatments, the mNSS scores of sham group, model group and experimental group were (0.10±0.02), (2.60±0.45) and (1.50±0.20) points; the cerebral infarction rates were (0.89±0.11)%, (32.56±4.12)% and (18.56±2.52)%; the cerebral water content were (68.25±7.05)%, (88.87±9.26)% and (71.11±8.11)%; the latent period were (22.60±2.86), (38.60±4.11) and (25.50±3.33) s; the platform residence time were (125.50±17.68), (80.60±9.68) and (115.80±13.89) s; the platform crossing times were (2.80±0.35), (0.70±0.09) and (1.80±0.30) times; the apoptosis rates were (6.65±0.74)%, (21.88±3.05)% and (13.62±2.62)%; the tumor necrosis factor-α levels were (30.05±3.85), (121.61±18.85) and (82.14±11.65) pg·mL-1; the levels of interleukin-1 beta were (92.55±12.15), (321.25±41.24) and (212.32±25.61) pg·mL-1; interleukin-6 levels were (184.32±20.54), (275.62±31.12) and (208.65±22.65) pg·mL-1; UCH-L1 protein levels were 1.00±0.22, 1.75±0.34 and 1.40±0.28; BDNF protein levels were 1.00±0.21, 1.68±0.38 and 2.54±0.41. There were statistically significant differences between sham group and model group (P<0.01, P<0.001). There were statistically significant differences between model group and experimental group (P<0.05, P<0.001).

Conclusion

GM1 can improve nerve cell apoptosis and inflammatory response by activating UCH-L1/BDNF signaling pathway, and play a protective role in neonatal rat HIBD.

monosialotetrahexosylganglioside  /  ubiquitin carboxy-terminal hydrolase 1  /  brain-derived neurotrophic factor  /  hypoxic ischemic brain injury  /  nerve cell  /  neonatal rat
Er-qing XING, Yu ZHANG, Jia-xing SHANG, Cheng-xiang WANG, Sui-liang XIE, Xiang-hua WANG, Wen-ting DOU. Monosialotetrahexosylganglioside protects brain injury in neonatal rats based on the UCH-L1/BDNF pathway[J]. Chinese Journal of Clinical Pharmacology, 2025 , 41 (4) : 512 -516 . DOI: 10.13699/j.cnki.1001-6821.2025.04.013
Year 2025 volume 41 Issue 4
PDF
1
0
Cite this Article
BibTeX
Article Info
doi: 10.13699/j.cnki.1001-6821.2025.04.013
  • Receive Date:2024-09-20
  • Online Date:2026-08-04
  • Published:2025-02-28
Article Data
Affiliations
History
  • Received:2024-09-20
Funding
Affiliations
    1a.Pediatric Ward 1, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
    1b.Pediatrics, Neonatology Eastern, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
    1c.Cardiovascular Medicine, Xinxiang Central Hospital (The Fourth Clinical College of Xinxiang Medical College), Xinxiang 453000, Henan Province, China
References
Share
https://castjournals.cast.org.cn/joweb/zglcylxzz/EN/10.13699/j.cnki.1001-6821.2025.04.013
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT