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1.
Int J Mol Sci ; 23(3)2022 Jan 21.
Artigo em Inglês | MEDLINE | ID: mdl-35163098

RESUMO

Brachial plexus avulsion (BPA) causes peripheral nerve injury complications with motor and sensory dysfunction of the upper limb. Growing evidence has shown an active role played by cold-water swimming (CWS) in alleviating peripheral neuropathic pain and functional recovery. This study examined whether CWS could promote functional recovery and pain modulation through the reduction of neuroinflammation and microglial overactivation in dorsal horn neurons at the early-stage of BPA. After BPA surgery was performed on rats, they were assigned to CWS or sham training for 5 min twice a day for two weeks. Functional behavioral responses were tested before and after BPA surgery, and each week during training. Results after the two-week training program showed significant improvements in BPA-induced motor and sensory loss (p < 0.05), lower inflammatory cell infiltration, and vacuole formation in injured nerves among the BPA-CWS group. Moreover, BPA significantly increased the expression of SP and IBA1 in dorsal horn neurons (p < 0.05), whereas CWS prevented their overexpression in the BPA-CWS group. The present findings evidenced beneficial rehabilitative effects of CWS on functional recovery and pain modulation at early-stage BPA. The beneficial effects are partially related to inflammatory suppression and spinal modulation. The synergistic role of CWS combined with other management approaches merits further investigation.


Assuntos
Neuropatias do Plexo Braquial/complicações , Plexo Braquial/lesões , Temperatura Baixa , Neuralgia/reabilitação , Recuperação de Função Fisiológica , Traumatismos da Coluna Vertebral/reabilitação , Natação , Animais , Modelos Animais de Doenças , Masculino , Neuralgia/etiologia , Neuralgia/patologia , Ratos , Ratos Sprague-Dawley , Traumatismos da Coluna Vertebral/etiologia , Traumatismos da Coluna Vertebral/patologia , Água
2.
Int J Mol Sci ; 22(18)2021 Sep 14.
Artigo em Inglês | MEDLINE | ID: mdl-34576074

RESUMO

Masticatory myofascial pain (MMP) is one of the most common causes of chronic orofacial pain in patients with temporomandibular disorders. To explore the antinociceptive effects of ultra-low frequency transcutaneous electrical nerve stimulation (ULF-TENS) on alterations of pain-related biochemicals, electrophysiology and jaw-opening movement in an animal model with MMP, a total of 40 rats were randomly and equally assigned to four groups; i.e., animals with MMP receiving either ULF-TENS or sham treatment, as well as those with sham-MMP receiving either ULF-TENS or sham treatment. MMP was induced by electrically stimulated repetitive tetanic contraction of masticatory muscle for 14 days. ULF-TENS was then performed at myofascial trigger points of masticatory muscles for seven days. Measurable outcomes included maximum jaw-opening distance, prevalence of endplate noise (EPN), and immunohistochemistry for substance P (SP) and µ-opiate receptors (MOR) in parabrachial nucleus and c-Fos in rostral ventromedial medulla. There were significant improvements in maximum jaw-opening distance and EPN prevalence after ULF-TENS in animals with MMP. ULF-TENS also significantly reduced SP overexpression, increased MOR expression in parabrachial nucleus, and increased c-Fos expression in rostral ventromedial medulla. ULF-TENS may represent a novel and applicable therapeutic approach for improvement of orofacial pain induced by MMP.


Assuntos
Dor Crônica/complicações , Dor Crônica/terapia , Transtornos da Articulação Temporomandibular/complicações , Transtornos da Articulação Temporomandibular/fisiopatologia , Estimulação Elétrica Nervosa Transcutânea , Animais , Dor Crônica/fisiopatologia , Modelos Animais de Doenças , Eletromiografia , Fenômenos Eletrofisiológicos , Músculos da Mastigação/fisiopatologia , Placa Motora/fisiopatologia , Síndromes da Dor Miofascial/complicações , Síndromes da Dor Miofascial/fisiopatologia , Síndromes da Dor Miofascial/terapia , Núcleos Parabraquiais/metabolismo , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Receptores Opioides mu/metabolismo , Substância P/metabolismo
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