-
Je něco špatně v tomto záznamu ?
3-N-Butylphthalide Confers Antiarrhythmic Features in Ischemia/Reperfusion Injury of Diabetic Heart by Targeting Mitochondria-Endoplasmic Reticulum Network and Inhibiting Oxidative Stress and Inflammation
R. Han, B. Duan
Status minimální 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
- antiarytmika farmakologie terapeutické užití MeSH
- benzofurany * farmakologie terapeutické užití MeSH
- experimentální diabetes mellitus * metabolismus farmakoterapie komplikace MeSH
- krysa rodu rattus MeSH
- oxidační stres * účinky léků MeSH
- potkani Sprague-Dawley * MeSH
- reperfuzní poškození myokardu * metabolismus farmakoterapie prevence a kontrola MeSH
- srdeční arytmie * etiologie prevence a kontrola metabolismus farmakoterapie MeSH
- srdeční mitochondrie metabolismus účinky léků MeSH
- stres endoplazmatického retikula * účinky léků MeSH
- zánět metabolismus farmakoterapie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
While 3-N-butylphthalide (NBP) has demonstrated notable cardioprotective effects, its precise role in mitigating myocardial arrhythmia following ischemia/reperfusion (IR) injury in diabetes remains unclear. This study aimed to explore the potential mechanisms through which NBP mitigates reperfusion-induced myocardial arrhythmia in diabetic rats, with a particular focus on mitochondrial function and biogenesis, endoplasmic reticulum (ER) stress, and oxidative/inflammatory responses. Sixty Sprague-Dawley rats were divided into non-diabetic and diabetic groups, subjected to in-vivo myocardial IR injury, and treated with NBP (100 mg/kg, intraperitoneally) through different modalities: preconditioning, postconditioning, or a combination of both. Electrocardiography (ECG) was employed to assess the incidence and severity of arrhythmia. Fluorometric, Western blotting and ELISA analyses were utilized to measure the mitochondrial, ER stress, and cellular outcomes. Treatment of non-diabetic rats with NBP in preconditioned, postconditioned, and combined approaches significantly reduced cardiotroponin-I and the frequency and severity of arrhythmias induced by IR injury. However, only the combined preconditioning plus postconditioning approach of NBP had protective and antiarrhythmic effects in diabetic rats, in an additive manner. Moreover, the NBP combined approach improved mitochondrial function and upregulated the expression of PGC-1?, Sirt1, and glutathione while concurrently downregulating ER stress and oxidative and pro-inflammatory-related proteins in diabetic rats. In conclusion, the combined approach of NBP treatment was effective in mitigating myocardial arrhythmia in diabetic rats. This approach coordinates interactions within the mitochondria-endoplasmic reticulum network and inhibits oxidative and inflammatory mediators, offering a promising strategy for managing myocardial arrhythmia in diabetic patients. Key words: Myocardial Infarction, Mitochondria, Arrhythmia, Reperfusion, Diabetes, Ischemia.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc24017608
- 003
- CZ-PrNML
- 005
- 20250312151313.0
- 007
- ta
- 008
- 241004s2024 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.935307 $2 doi
- 035 __
- $a (PubMed)39264076
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Han, R $u Department of Cardiac Surgery, First Affiliated Hospital of Kunming Medical University, Kunming, China. pikachu615@sina.com
- 245 10
- $a 3-N-Butylphthalide Confers Antiarrhythmic Features in Ischemia/Reperfusion Injury of Diabetic Heart by Targeting Mitochondria-Endoplasmic Reticulum Network and Inhibiting Oxidative Stress and Inflammation / $c R. Han, B. Duan
- 520 9_
- $a While 3-N-butylphthalide (NBP) has demonstrated notable cardioprotective effects, its precise role in mitigating myocardial arrhythmia following ischemia/reperfusion (IR) injury in diabetes remains unclear. This study aimed to explore the potential mechanisms through which NBP mitigates reperfusion-induced myocardial arrhythmia in diabetic rats, with a particular focus on mitochondrial function and biogenesis, endoplasmic reticulum (ER) stress, and oxidative/inflammatory responses. Sixty Sprague-Dawley rats were divided into non-diabetic and diabetic groups, subjected to in-vivo myocardial IR injury, and treated with NBP (100 mg/kg, intraperitoneally) through different modalities: preconditioning, postconditioning, or a combination of both. Electrocardiography (ECG) was employed to assess the incidence and severity of arrhythmia. Fluorometric, Western blotting and ELISA analyses were utilized to measure the mitochondrial, ER stress, and cellular outcomes. Treatment of non-diabetic rats with NBP in preconditioned, postconditioned, and combined approaches significantly reduced cardiotroponin-I and the frequency and severity of arrhythmias induced by IR injury. However, only the combined preconditioning plus postconditioning approach of NBP had protective and antiarrhythmic effects in diabetic rats, in an additive manner. Moreover, the NBP combined approach improved mitochondrial function and upregulated the expression of PGC-1?, Sirt1, and glutathione while concurrently downregulating ER stress and oxidative and pro-inflammatory-related proteins in diabetic rats. In conclusion, the combined approach of NBP treatment was effective in mitigating myocardial arrhythmia in diabetic rats. This approach coordinates interactions within the mitochondria-endoplasmic reticulum network and inhibits oxidative and inflammatory mediators, offering a promising strategy for managing myocardial arrhythmia in diabetic patients. Key words: Myocardial Infarction, Mitochondria, Arrhythmia, Reperfusion, Diabetes, Ischemia.
- 650 _2
- $a zvířata $7 D000818
- 650 12
- $a potkani Sprague-Dawley $7 D017207
- 650 12
- $a oxidační stres $x účinky léků $7 D018384
- 650 12
- $a reperfuzní poškození myokardu $x metabolismus $x farmakoterapie $x prevence a kontrola $7 D015428
- 650 12
- $a benzofurany $x farmakologie $x terapeutické užití $7 D001572
- 650 12
- $a experimentální diabetes mellitus $x metabolismus $x farmakoterapie $x komplikace $7 D003921
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 12
- $a srdeční arytmie $x etiologie $x prevence a kontrola $x metabolismus $x farmakoterapie $7 D001145
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 12
- $a stres endoplazmatického retikula $x účinky léků $7 D059865
- 650 _2
- $a antiarytmika $x farmakologie $x terapeutické užití $7 D000889
- 650 _2
- $a srdeční mitochondrie $x metabolismus $x účinky léků $7 D008929
- 650 _2
- $a zánět $x metabolismus $x farmakoterapie $7 D007249
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Duan, B
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 73, č. 4 (2024), s. 529-541
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39264076 $y Pubmed
- 910 __
- $a ABA008 $b A 4120 $c 266 $y - $z 0
- 990 __
- $a 20241004 $b ABA008
- 991 __
- $a 20250312151320 $b ABA008
- 999 __
- $a min $b bmc $g 2283520 $s 1229558
- BAS __
- $a 3
- BAS __
- $a PreBMC-MEDLINE
- BMC __
- $a 2024 $b 73 $c 4 $d 529-541 $e 20240831 $i 1802-9973 $m Physiological research $n Physiol Res $x MED00003824
- LZP __
- $a Pubmed-20241004