-
Je něco špatně v tomto záznamu ?
Bergaptol Ameliorates Insulin Sensitivity in Gestational Diabetes Mellitus by Inhibiting the Inflammatory Pathway in Streptozotocin-Induced Diabetic Rats
Q. Li, J. Chen, Z. Wang, L. Zhuang, Z. Yu, D. Yang
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
PubMed Central
od 2020
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- experimentální diabetes mellitus * farmakoterapie metabolismus MeSH
- gestační diabetes * farmakoterapie metabolismus MeSH
- inzulinová rezistence * fyziologie MeSH
- kinasa glykogensynthasy 3beta metabolismus MeSH
- krevní glukóza metabolismus účinky léků MeSH
- krysa rodu rattus MeSH
- oxidační stres účinky léků MeSH
- potkani Wistar MeSH
- receptor inzulinu metabolismus MeSH
- signální transdukce účinky léků MeSH
- simulace molekulového dockingu * MeSH
- těhotenství MeSH
- zánět farmakoterapie metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- těhotenství MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Investigation determines the beneficial effect of bergaptol against gestational diabetes (GD). Gestational diabetes was induced in female rats and treated them with bergaptol 20 and 40 mg/kg for eighteen days. Effect of bergaptol was assessed on blood glucose and insulin level in GD rat. Inflammatory mediators and oxidative stress parameters were also assessed in GD rats. Moreover, mRNA expression of INSR, NF-kappaB, Akt and GSK-3beta were assessed in the GD rats by qRT-PCR method. In silico network pharmacology study was performed, along with gene ontology and egg pathway to assessed the targets of bergaptol, molecular docking study was also performed for the confirmation of possible pathway involved in the management of GD. Blood glucose and insulin level was significantly reduces in the blood bergaptol treated group than GD group of rats. Treatment with bergaptol ameliorates the altered level of mediators of inflammation and oxidative stress parameters in GD rats. There was significant reduction in the mRNA expression of NF-kappaB and GSK-3beta and increase in expression of INSR and Akt in the tissue homogenate of bergaptol treated GD rats. Docking study shows effective binding strength of bergaptol individually with INSR, NF-kappaB, Akt and GSK-3beta-protein targets. In conclusion, data of investigation suggest that bergaptol improves the sensitivity of insulin receptor in GD, as it reduces parameters of oxidative stress and inflammatory mediators by regulating INSR/NF-kappaB/Akt/GSK-3beta pathway. Key words Gestational diabetes, Bergaptol, Insulin resistance, Inflammation, Oxidative stress.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25008993
- 003
- CZ-PrNML
- 005
- 20250502104908.0
- 007
- ta
- 008
- 250411s2025 xr d f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.935474 $2 doi
- 035 __
- $a (PubMed)40126146
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Li, Q. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China. yangdan424@outlook.com
- 245 10
- $a Bergaptol Ameliorates Insulin Sensitivity in Gestational Diabetes Mellitus by Inhibiting the Inflammatory Pathway in Streptozotocin-Induced Diabetic Rats / $c Q. Li, J. Chen, Z. Wang, L. Zhuang, Z. Yu, D. Yang
- 520 9_
- $a Investigation determines the beneficial effect of bergaptol against gestational diabetes (GD). Gestational diabetes was induced in female rats and treated them with bergaptol 20 and 40 mg/kg for eighteen days. Effect of bergaptol was assessed on blood glucose and insulin level in GD rat. Inflammatory mediators and oxidative stress parameters were also assessed in GD rats. Moreover, mRNA expression of INSR, NF-kappaB, Akt and GSK-3beta were assessed in the GD rats by qRT-PCR method. In silico network pharmacology study was performed, along with gene ontology and egg pathway to assessed the targets of bergaptol, molecular docking study was also performed for the confirmation of possible pathway involved in the management of GD. Blood glucose and insulin level was significantly reduces in the blood bergaptol treated group than GD group of rats. Treatment with bergaptol ameliorates the altered level of mediators of inflammation and oxidative stress parameters in GD rats. There was significant reduction in the mRNA expression of NF-kappaB and GSK-3beta and increase in expression of INSR and Akt in the tissue homogenate of bergaptol treated GD rats. Docking study shows effective binding strength of bergaptol individually with INSR, NF-kappaB, Akt and GSK-3beta-protein targets. In conclusion, data of investigation suggest that bergaptol improves the sensitivity of insulin receptor in GD, as it reduces parameters of oxidative stress and inflammatory mediators by regulating INSR/NF-kappaB/Akt/GSK-3beta pathway. Key words Gestational diabetes, Bergaptol, Insulin resistance, Inflammation, Oxidative stress.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a gestační diabetes $x farmakoterapie $x metabolismus $7 D016640
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a těhotenství $7 D011247
- 650 12
- $a experimentální diabetes mellitus $x farmakoterapie $x metabolismus $7 D003921
- 650 12
- $a inzulinová rezistence $x fyziologie $7 D007333
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 12
- $a simulace molekulového dockingu $7 D062105
- 650 _2
- $a oxidační stres $x účinky léků $7 D018384
- 650 _2
- $a potkani Wistar $7 D017208
- 650 _2
- $a signální transdukce $x účinky léků $7 D015398
- 650 _2
- $a krevní glukóza $x metabolismus $x účinky léků $7 D001786
- 650 _2
- $a zánět $x farmakoterapie $x metabolismus $7 D007249
- 650 _2
- $a kinasa glykogensynthasy 3beta $x metabolismus $7 D000071679
- 650 _2
- $a receptor inzulinu $x metabolismus $7 D011972
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Chen, J. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 700 1_
- $a Wang, Z. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 700 1_
- $a Zhuang, L. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 700 1_
- $a Yu, Z. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 700 1_
- $a Yang, D. $u Department of Obstetrics, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 74, č. 1 (2025), s. 93-104
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/40126146 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y p $z 0
- 990 __
- $a 20250411 $b ABA008
- 991 __
- $a 20250502104900 $b ABA008
- 999 __
- $a ok $b bmc $g 2307244 $s 1246071
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2025 $b 74 $c 1 $d 93-104 $e 20250324 $i 1802-9973 $m Physiological research $n Physiol Res $x MED00003824
- LZP __
- $b NLK116 $a Pubmed-20250411