• Je něco špatně v tomto záznamu ?

Enhancement of Cognitive Function in Rats with Vascular Dementia Through Modulation of the Nrf2/GPx4 Signaling Pathway by High-Frequency Repetitive Transcranial Magnetic Stimulation

WJ. Jin, XX. Zhu, KT. Luo, S. Wang, JA. Li, LF. Qian, GX. Xu

. 2024 ; 73 (5) : 857-868. [pub] 20241119

Status minimální Jazyk angličtina Země Česko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24022797

Repetitive transcranial magnetic stimulation (rTMS) represents a non-invasive therapeutic modality acknowledged for augmenting neurological function recovery following stroke. Nonetheless, uncertainties remain regarding its efficacy in promoting cognitive function recovery in patients diagnosed with vascular dementia (VD). In this study, VD was experimentally induced in a rat model utilizing the bilateral common carotid artery occlusion method. Following a recuperation period of seven days, rats were subjected to high-frequency repetitive transcranial magnetic stimulation (HF-rTMS) at a frequency of 10 Hz. Cognitive function was assessed utilizing the Morris water maze test, and the levels of IL-6, TNF-alpha, SOD, GSH, MDA, and Fe2+ in cerebral tissue were quantitatively analyzed through enzyme-linked immunosorbent assay. Moreover, the gene and protein expressions of nuclear factor erythroid 2-related factor 2 (Nrf2) and glutathione peroxidase 4 (GPx4) were meticulously investigated via quantitative polymerase chain reaction (qPCR) and Western blotting techniques. The use of HF-rTMS notably augmented cognitive function in rats with VD, concomitantly reducing neuroinflammation, oxidative stress, and ferroptosis within the brain. The group subjected to HF-rTMS demonstrated an increase in the levels of both proteins and genes associated with Nrf2 and GPx4, in comparison to the VD group. These results highlight the potential of HF-rTMS treatment in enhancing cognitive function in rats diagnosed with VD through the modulation of the Nrf2/GPx4 signaling pathway. This modulation, in turn, mitigates processes linked with neuroinflammation, oxidative stress, and ferroptosis. Nevertheless, additional studies are essential to comprehensively elucidate the underlying mechanisms and clinical implications of HF-rTMS treatment in the treatment of VD.

000      
00000naa a2200000 a 4500
001      
bmc24022797
003      
CZ-PrNML
005      
20250312151309.0
007      
ta
008      
241205s2024 xr f 000 0|eng||
009      
AR
035    __
$a (PubMed)39560194
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xr
100    1_
$a Jin, W-J $u Department of Rehabilitation Medicine, Nanjing Medical University, Nanjing, China; Rehabilitation Medicine Center, Zhejiang Chinese Medical University Affiliated Jiaxing TCM Hospital, Jiaxing, China. xuguangxu1@126.com
245    10
$a Enhancement of Cognitive Function in Rats with Vascular Dementia Through Modulation of the Nrf2/GPx4 Signaling Pathway by High-Frequency Repetitive Transcranial Magnetic Stimulation / $c WJ. Jin, XX. Zhu, KT. Luo, S. Wang, JA. Li, LF. Qian, GX. Xu
520    9_
$a Repetitive transcranial magnetic stimulation (rTMS) represents a non-invasive therapeutic modality acknowledged for augmenting neurological function recovery following stroke. Nonetheless, uncertainties remain regarding its efficacy in promoting cognitive function recovery in patients diagnosed with vascular dementia (VD). In this study, VD was experimentally induced in a rat model utilizing the bilateral common carotid artery occlusion method. Following a recuperation period of seven days, rats were subjected to high-frequency repetitive transcranial magnetic stimulation (HF-rTMS) at a frequency of 10 Hz. Cognitive function was assessed utilizing the Morris water maze test, and the levels of IL-6, TNF-alpha, SOD, GSH, MDA, and Fe2+ in cerebral tissue were quantitatively analyzed through enzyme-linked immunosorbent assay. Moreover, the gene and protein expressions of nuclear factor erythroid 2-related factor 2 (Nrf2) and glutathione peroxidase 4 (GPx4) were meticulously investigated via quantitative polymerase chain reaction (qPCR) and Western blotting techniques. The use of HF-rTMS notably augmented cognitive function in rats with VD, concomitantly reducing neuroinflammation, oxidative stress, and ferroptosis within the brain. The group subjected to HF-rTMS demonstrated an increase in the levels of both proteins and genes associated with Nrf2 and GPx4, in comparison to the VD group. These results highlight the potential of HF-rTMS treatment in enhancing cognitive function in rats diagnosed with VD through the modulation of the Nrf2/GPx4 signaling pathway. This modulation, in turn, mitigates processes linked with neuroinflammation, oxidative stress, and ferroptosis. Nevertheless, additional studies are essential to comprehensively elucidate the underlying mechanisms and clinical implications of HF-rTMS treatment in the treatment of VD.
650    _2
$a zvířata $7 D000818
650    12
$a faktor 2 související s NF-E2 $x metabolismus $7 D051267
650    12
$a vaskulární demence $x metabolismus $x terapie $x psychologie $7 D015140
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a krysa rodu Rattus $7 D051381
650    12
$a transkraniální magnetická stimulace $x metody $7 D050781
650    12
$a signální transdukce $7 D015398
650    12
$a kognice $x fyziologie $7 D003071
650    12
$a fosfolipidová hydroperoxidglutathionperoxidasa $x metabolismus $7 D000080662
650    _2
$a oxidační stres $7 D018384
650    _2
$a potkani Sprague-Dawley $7 D017207
650    _2
$a potkani Wistar $7 D017208
650    _2
$a modely nemocí na zvířatech $7 D004195
655    _2
$a časopisecké články $7 D016428
700    1_
$a Zhu, X-X
700    1_
$a Luo, K-T
700    1_
$a Wang, S
700    1_
$a Li, J-A
700    1_
$a Qian, L-F
700    1_
$a Xu, G-X
773    0_
$w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 73, č. 5 (2024), s. 857-868
856    41
$u https://pubmed.ncbi.nlm.nih.gov/39560194 $y Pubmed
910    __
$a ABA008 $b A 4120 $c 266 $y - $z 0
990    __
$a 20241205 $b ABA008
991    __
$a 20250312151316 $b ABA008
999    __
$a min $b bmc $g 2283526 $s 1234802
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 73 $c 5 $d 857-868 $e 20241119 $i 1802-9973 $m Physiological research $n Physiol Res $x MED00003824
LZP    __
$a Pubmed-20241205

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...