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1.
Dermatol Surg ; 50(6): 527-533, 2024 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-38518110

RESUMO

BACKGROUND: Despite the widespread use of botulinum toxin (BTX) injection for the treatment of masseter muscle hypertrophy (MMH), there is no standard treatment option. OBJECTIVE: We report the efficacy and safety for BTX in MMH over a period of 48 weeks. METHODS: In double-blinded, placebo-controlled phase 3 trials, 180 patients (randomized 1:1) received treatment with placebo (normal saline) or prabotulinumtoxinA (48 units). Masseter muscle thickness (at maximal clenching and resting positions), 3D imaging analysis, and masseter muscle hypertrophy scale grades were analyzed at each time point. After the 24-week CORE study, all patients who met the same criteria of the CORE study at week 24 ( n = 114) received only prabotulinumtoxinA, regardless of previous treatment, for an additional 24 weeks (48 weeks in total) for the open-label extension study. RESULTS: The largest differences in mean and percent changes from baseline in masseter muscle thickness were observed at 12 weeks, and there were significant differences between the 2 groups at all time points (all p < .001). The effect was independent of the number of injections. No serious adverse event was observed. CONCLUSION: PrabotulinumtoxinA could effectively ameliorate MMH without major complications.


Assuntos
Toxinas Botulínicas Tipo A , Hipertrofia , Músculo Masseter , Humanos , Toxinas Botulínicas Tipo A/administração & dosagem , Toxinas Botulínicas Tipo A/efeitos adversos , Método Duplo-Cego , Hipertrofia/tratamento farmacológico , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/patologia , Músculo Masseter/anormalidades , Feminino , Pessoa de Meia-Idade , Adulto , Masculino , Resultado do Tratamento , Fármacos Neuromusculares/administração & dosagem , Fármacos Neuromusculares/efeitos adversos , Injeções Intramusculares
2.
J Oral Rehabil ; 51(9): 1759-1769, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-38840501

RESUMO

BACKGROUND: It remains unclear how the salivary flow and the fat content of food affect bolus formation during mastication. OBJECTIVES: We aimed to clarify: (1) how hyposalivation affects jaw-closing and hyoid-elevating muscle activities in bolus formation, and (2) if the effect of hyposalivation on muscle activity depends on the fat content of food. METHODS: Eighteen healthy male volunteers were instructed to freely ingest four test foods: Plain, Fat without seasoning, Fat with seasoning, and Soft rice crackers. Masseter and suprahyoid electromyographic activities were recorded before and 30 min after the administration of atropine sulfate, a muscarinic receptor antagonist that induces hyposalivation. RESULTS: Hyposalivation extended the masticatory duration significantly in all the test foods except Fat with seasoning. Masticatory cycle time was significantly longer with vs without hyposalivation for the Soft (p = .011). Suprahyoid activity/cycle was significantly greater with vs without hyposalivation (p = .013). Masticatory cycle time was significantly longer at the late stage with vs without hyposalivation for the Soft (p < .001). Suprahyoid activity/cycle was significantly greater at the middle (p = .045) and late stages (p = .002) with vs without hyposalivation for the Soft and greater at the late stage with vs without hyposalivation for the Plain (p = .043). Changes in masticatory cycle time and suprahyoid activity/cycle for these foods had significantly positive relationship (p < .001). CONCLUSION: Hyposalivation-induced changes in masticatory behaviours resulted from the middle and late stage suprahyoid activity. Fat content and seasoning compensate for salivary flow inhibition.


Assuntos
Eletromiografia , Voluntários Saudáveis , Mastigação , Saliva , Humanos , Masculino , Mastigação/fisiologia , Adulto , Saliva/química , Xerostomia/fisiopatologia , Adulto Jovem , Salivação/efeitos dos fármacos , Salivação/fisiologia , Músculo Masseter/fisiologia , Músculo Masseter/efeitos dos fármacos , Gorduras na Dieta , Atropina/farmacologia
3.
Aesthet Surg J ; 44(8): NP567-NP573, 2024 Jul 15.
Artigo em Inglês | MEDLINE | ID: mdl-38494986

RESUMO

BACKGROUND: The injection of botulinum toxin into the masseter muscle is an important method for improving hypertrophy. However, some patients may experience adverse reactions, such as sagging of the lower jaw. Therefore, we proposed a method of injecting botulinum toxin into the masseter and platysma muscles that would reduce masseter size and enhance the jawline. OBJECTIVES: The aim of this study was to reduce the masseter size while enhancing the jawline. METHODS: Twenty patients received botulinum toxin injections into the masseter and platysma muscles. Pain levels were evaluated with the visual analog scale. All patients were photographed before and 6 months after treatment. Evaluations were performed based on standardized criteria. The lift index, reduction index, and symmetry index were performed to assess the degree of jawline elevation, masseter size reduction, and jawline symmetry before and after treatment. RESULTS: The mean visual analog scale score of the 20 patients was 2.80 (±1.24). The mean lift index score decreased from 4.93 (±0.34) to 4.53 (±0.37), P < .05. The mean reduction index score decreased from 3.13 (±0.27) to 2.74 (±0.27), P < .05. The mean symmetry index score changed from 0.0393 (±0.0296) to 0.0257 (±0.0246), P < .05. CONCLUSIONS: Botulinum toxin injections into the masseter and platysma muscles through nerve block reduced the masseter size, elevated the jawline, and improved symmetry.


Assuntos
Toxinas Botulínicas Tipo A , Hipertrofia , Músculo Masseter , Humanos , Músculo Masseter/efeitos dos fármacos , Feminino , Injeções Intramusculares/métodos , Adulto , Toxinas Botulínicas Tipo A/administração & dosagem , Toxinas Botulínicas Tipo A/efeitos adversos , Masculino , Pessoa de Meia-Idade , Resultado do Tratamento , Hipertrofia/tratamento farmacológico , Fármacos Neuromusculares/administração & dosagem , Fármacos Neuromusculares/efeitos adversos , Técnicas Cosméticas/efeitos adversos , Medição da Dor , Adulto Jovem
4.
Nutr Neurosci ; 24(12): 927-939, 2021 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31766953

RESUMO

Purpose Children with cerebral palsy (CP) often exhibit difficulties in feeding resulting from deficits in chewing. This study investigates the therapeutic potential of L-tryptophan (TRI) to reduce deficits in chewing in rats subjected to an experimental model of CP.Methods A total of 80 Wistar albino rats were used. Pups were randomly assigned to 4 experimental groups: Control Saline, Control TRI, CP Saline, and CP TRI groups. The experimental model of CP was based on the combination of perinatal anoxia associated with postnatal sensorimotor restriction of the hind limbs. TRI was administered subcutaneously during the lactation period. Anatomical and behavioral parameters were evaluated during maturation, including body weight gain, food intake, chewing movements, relative weight and the distribution of the types of masseter muscle fibers.Results The induction of CP limited body weight gain, decreased food intake and led to impairment in the morphological and functional parameters of chewing. Moreover, for a comparable amount of food ingested, CP TRI animals grew the most. In addition, supplementation with TRI improved the number of chewing movements, and increased the weight and proportion of type IIB fibers of the masseter in rats subjected to CP.Conclusion These results demonstrate that experimental CP impaired the development of mastication and that TRI supplementation increased masticatory maturation in animals subjected to CP.


Assuntos
Paralisia Cerebral/fisiopatologia , Mastigação/efeitos dos fármacos , Mastigação/fisiologia , Triptofano/uso terapêutico , Animais , Paralisia Cerebral/tratamento farmacológico , Modelos Animais de Doenças , Ingestão de Alimentos , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/fisiopatologia , Fenótipo , Ratos , Ratos Wistar , Aumento de Peso/efeitos dos fármacos
5.
Anesth Analg ; 128(4): 652-659, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30768455

RESUMO

At a recent consensus conference, the Malignant Hyperthermia Association of the United States addressed 6 important and unresolved clinical questions concerning the optimal management of patients with malignant hyperthermia (MH) susceptibility or acute MH. They include: (1) How much dantrolene should be available in facilities where volatile agents are not available or administered, and succinylcholine is only stocked on site for emergency purposes? (2) What defines masseter muscle rigidity? What is its relationship to MH, and how should it be managed when it occurs? (3) What is the relationship between MH susceptibility and heat- or exercise-related rhabdomyolysis? (4) What evidence-based interventions should be recommended to alleviate hyperthermia associated with MH? (5) After treatment of acute MH, how much dantrolene should be administered and for how long? What criteria should be used to determine stopping treatment with dantrolene? (6) Can patients with a suspected personal or family history of MH be safely anesthetized before diagnostic testing? This report describes the consensus process and the outcomes for each of the foregoing unanswered clinical questions.


Assuntos
Dantroleno/provisão & distribuição , Hipertermia Maligna/terapia , Músculo Masseter/efeitos dos fármacos , Rabdomiólise/terapia , Succinilcolina/provisão & distribuição , Consenso , Dantroleno/uso terapêutico , Esquema de Medicação , Medicina Baseada em Evidências , Exercício Físico , Humanos , Relaxantes Musculares Centrais/provisão & distribuição , Relaxantes Musculares Centrais/uso terapêutico , Fármacos Neuromusculares Despolarizantes/provisão & distribuição , Fármacos Neuromusculares Despolarizantes/uso terapêutico , Rabdomiólise/complicações , Sociedades Médicas , Succinilcolina/uso terapêutico , Resultado do Tratamento , Estados Unidos
6.
Dermatol Surg ; 45(4): 566-572, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30883483

RESUMO

BACKGROUND: Cultural ideals for a slimmer face have led to an upsurge in interest in facial contouring among East Asians. Although surgical resection has traditionally been the main treatment option, botulinum toxin injection is becoming a popular, noninvasive alternative. OBJECTIVE: To describe the use of botulinum toxin injection for masseter reduction in East Asians. METHODS: An electronic search of the PubMed database was performed for studies published from 2000 to 2017 that meet the word combination of botulinum toxin, masseter, hypertrophy, and/or lower face contouring. Only the studies conducted in East Asian countries were analyzed in this review, exception of one study from Thailand. RESULTS: A total of 12 publications were identified. Each study was reviewed to extract relevant information on patient selection, injection techniques, efficacy, dosage, frequency, and main side effects of treating masseters with botulinum toxin. CONCLUSION: Botulinum toxin injection for masseter reduction in East Asians is efficacious and generally considered safe with no significant side effects. Future areas for investigation include defining the criteria for benign masseteric hypertrophy, minimum effective dosage of botulinum toxin, and the potential long-term effects of the injection.


Assuntos
Toxinas Botulínicas Tipo A/administração & dosagem , Hipertrofia/diagnóstico , Hipertrofia/terapia , Músculo Masseter/anormalidades , Músculo Masseter/efeitos dos fármacos , Fármacos Neuromusculares/administração & dosagem , Povo Asiático , Técnicas Cosméticas , Face/anatomia & histologia , Humanos , Injeções Intramusculares
7.
Ann Plast Surg ; 82(1S Suppl 1): S29-S32, 2019 01.
Artigo em Inglês | MEDLINE | ID: mdl-30540604

RESUMO

INTRODUCTION: Botulinum neurotoxin A (BoNT-A) is a minimally invasive and technically straightforward treatment of masseter muscle (MM) volume reduction and facial contouring, but the literature on its long-term effect on MM volume remains unclear. OBJECTIVE: This study aimed to assess quantitatively for progressive volume changes of lower facial contour after 3 BoNT-A injections in patients with bilateral MM hypertrophy causing square facial morphology using 3-dimensional computed tomographic scans. MATERIALS AND METHODS: Ten female patients with square facial morphology due to bilateral MM hypertrophy were recruited to, and 6 completed, this clinical study. Each received 24 U of BoNT-A into the inferior portion of each MM on both sides, repeated 6 monthly to complete 3 treatments. Masseter muscle volume changes were assessed using 3-dimensional computed tomography at pretreatment (before injections) and posttreatment (1 year after the third injection). RESULTS: Mean MM volume significantly reduced from 26.39 ± 4.18 cm before treatment to 23.26 ± 4.31 cm 1 year after treatment (P = 0.002). CONCLUSION: Three consecutive 6-monthly BoNT-A injections into the MMs reduced their volume by 12% when assessed 1 year after completion of treatment.


Assuntos
Toxinas Botulínicas Tipo A/uso terapêutico , Hipertrofia/diagnóstico por imagem , Hipertrofia/tratamento farmacológico , Imageamento Tridimensional , Músculo Masseter/anormalidades , Músculo Masseter/anatomia & histologia , Tomografia Computadorizada por Raios X/métodos , Adulto , Estética , Feminino , Humanos , Injeções Intralesionais , Injeções Intramusculares , Músculo Masseter/diagnóstico por imagem , Músculo Masseter/efeitos dos fármacos , Pessoa de Meia-Idade , Tamanho do Órgão/efeitos dos fármacos , Estudos de Amostragem , Estatísticas não Paramétricas , Resultado do Tratamento
8.
Am J Orthod Dentofacial Orthop ; 156(2): 193-202, 2019 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31375229

RESUMO

OBJECTIVES: To evaluate whether the effects on the mandibular condylar cartilage (MCC) and subchondral bone are transient of botulinum neurotoxin (Botox) injection into the masseter muscle. METHODS: Botox (0.3 U) was injected into the right masseter of 6-week-old female mice (C57BL/6; n = 16). In addition, 16 mice were used as control and received no injections. Experimental and matching control mice were killed 4 or 8 weeks after the single Botox injection. Mandibles and mandibular condyles were analyzed by means of microscopic computed tomography (microCT) and histology. Sagittal sections of condyles were stained for tartrate-resistant acid phosphatase (TRAP), toluidine blue, 5-ethynyl-2'-deoxyuridine (EdU), and terminal deoxynucleotide transferase-mediated dUTP nick-end labeling. RESULTS: Bone volume fraction was significantly decreased on the subchondral bone of the Botox-injected side, compared with the control side and control mice, 4 and 8 weeks after injection. Furthermore, histologic analysis revealed decrease in mineralization, cartilage thickness, TRAP activity, and EdU-positive cells in the MCC of the Botox-injected side 4 and 8 weeks after injection. CONCLUSIONS: The effects on the MCC and subchondral bone of Botox injection into the masseter muscle persisted for 8 weeks after injection and were not considered to be transient.


Assuntos
Toxinas Botulínicas Tipo A/farmacologia , Côndilo Mandibular/efeitos dos fármacos , Músculo Masseter/efeitos dos fármacos , Animais , Apoptose/efeitos dos fármacos , Proliferação de Células/efeitos dos fármacos , Feminino , Injeções , Masculino , Mandíbula , Côndilo Mandibular/diagnóstico por imagem , Côndilo Mandibular/patologia , Músculo Masseter/diagnóstico por imagem , Músculo Masseter/patologia , Camundongos , Camundongos Endogâmicos C57BL , Modelos Animais , Articulação Temporomandibular
9.
Mol Pain ; 14: 1744806918763270, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29448913

RESUMO

Background The mechanisms underlying tooth pulp hypersensitivity associated with masseter muscle hyperalgesia remain largely underinvestigated. In the present study, we aimed to determine whether masseter muscle contraction induced by daily electrical stimulation influences the mechanical head-withdrawal threshold and genioglossus electromyography activity caused by the application of capsaicin to the upper first molar tooth pulp. We further investigated whether astroglial glutamine synthesis is involved in first molar tooth pulp hypersensitivity associated with masseter muscle contraction. Methods The first molar tooth pulp was treated with capsaicin or vehicle in masseter muscle contraction or sham rats, following which the astroglial glutamine synthetase inhibitor methionine sulfoximine or Phosphate buffered saline (PBS) was applied. Astroglial activation was assessed via immunohistochemistry. Results The mechanical head-withdrawal threshold of the ipsilateral masseter muscle was significantly decreased in masseter muscle contraction rats than in sham rats. Genioglossus electromyography activity was significantly higher in masseter muscle contraction rats than sham rats. Glial fibrillary acidic protein-immunoreactive cell density was significantly higher in masseter muscle contraction rats than in sham rats. Administration of methionine sulfoximine induced no significant changes in the density of glial fibrillary acidic protein-immunoreactive cells relative to PBS treatment. However, mechanical head-withdrawal threshold was significantly higher in masseter muscle contraction rats than PBS-treated rats after methionine sulfoximine administration. Genioglossus electromyography activity following first molar tooth pulp capsaicin treatment was significantly lower in methionine sulfoximine-treated rats than in PBS-treated rats. In the ipsilateral region, the total number of phosphorylated extracellular signal-regulated protein kinase immunoreactive cells in the medullary dorsal horn was significantly smaller upon first molar tooth pulp capsaicin application in methionine sulfoximine-treated rats than in PBS-treated rats. Conclusions Our results suggest that masseter muscle contraction induces astroglial activation, and that this activation spreads from caudal to the obex in the medullary dorsal horn, resulting in enhanced neuronal excitability associated with astroglial glutamine synthesis in medullary dorsal horn neurons receiving inputs from the tooth pulp. These findings provide significant insight into the mechanisms underlying tooth pulp hypersensitivity associated with masseter muscle contraction.


Assuntos
Astrócitos/metabolismo , Polpa Dentária/metabolismo , Polpa Dentária/patologia , Glutamina/metabolismo , Músculo Masseter/fisiopatologia , Bulbo/metabolismo , Contração Muscular , Animais , Astrócitos/efeitos dos fármacos , Capsaicina/farmacologia , Polpa Dentária/efeitos dos fármacos , Polpa Dentária/fisiopatologia , Estimulação Elétrica , Eletromiografia , MAP Quinases Reguladas por Sinal Extracelular/metabolismo , Proteína Glial Fibrilar Ácida/metabolismo , Hiperalgesia/patologia , Hiperalgesia/fisiopatologia , Masculino , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/patologia , Bulbo/efeitos dos fármacos , Bulbo/fisiopatologia , Metionina Sulfoximina/administração & dosagem , Metionina Sulfoximina/farmacologia , Dente Molar/patologia , Contração Muscular/efeitos dos fármacos , Fosforilação/efeitos dos fármacos , Células do Corno Posterior/efeitos dos fármacos , Células do Corno Posterior/metabolismo , Ratos Sprague-Dawley
10.
Muscle Nerve ; 57(1): 96-99, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-28187528

RESUMO

INTRODUCTION: Botulinum neurotoxin A (BoNTA) has long been used as a therapeutic agent and has been widely accepted as a cosmetic agent in recent years. It can inhibit function and induce structural changes in skeletal muscle. METHODS: Specimens of fresh dissected human masseter muscle were used to observe the ultrastructural changes that occurred at 6 and 12 months following BoNTA injection. RESULTS: The findings observed were muscle fiber distortion, sarcomere shortening, mitochondrial vacuolar degeneration, glycogen accumulation, and H and M band disruption in the triad of tubules. At 12 months after injection, there was still evidence of degenerative changes in muscle ultrastructure, whereas most organelles exhibited a normal structure. DISCUSSION: Profound ultrastructural and organelle disfiguring changes were observed after BoNTA injection into human masseter muscle. Most changes were transient, however, and were resolved by 12 months after injection. Muscle Nerve 57: 96-99, 2018.


Assuntos
Toxinas Botulínicas Tipo A/farmacologia , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/ultraestrutura , Fármacos Neuromusculares/farmacologia , Adulto , Povo Asiático , Toxinas Botulínicas Tipo A/administração & dosagem , Face/anatomia & histologia , Feminino , Glicogênio/metabolismo , Humanos , Injeções Intramusculares , Músculo Masseter/metabolismo , Microscopia Eletrônica , Microtúbulos/metabolismo , Microtúbulos/patologia , Mitocôndrias Musculares/efeitos dos fármacos , Mitocôndrias Musculares/ultraestrutura , Fibras Musculares Esqueléticas/efeitos dos fármacos , Fibras Musculares Esqueléticas/ultraestrutura , Fármacos Neuromusculares/administração & dosagem , Sarcômeros/efeitos dos fármacos , Sarcômeros/ultraestrutura , Cirurgia Plástica , Adulto Jovem
11.
Aesthet Surg J ; 38(2): 192-198, 2018 Feb 17.
Artigo em Inglês | MEDLINE | ID: mdl-29117291

RESUMO

BACKGROUND: Botulinum toxin (BoNT) is widely used to treat masseter muscle hypertrophy. Changes in the muscle thickness have been found in many studies, but there has been no report on changes in the thickness from the skin surface to the masseter muscle. OBJECTIVES: We aimed to use ultrasonography to measure not only changes in the muscle thickness but also changes in subcutaneous thickness. METHODS: This study enrolled 20 volunteer patients: 10 were assigned to an experimental group (injected with each side 25 U of botulinum toxin into both masseter muscles) and 10 to a control group (injected with normal saline). The thicknesses were measured before the injection and at 4, 8, and 12 weeks after the injection both at rest and during maximum muscle contraction. RESULTS: The subcutaneous thickness did not differ significantly over time either at rest (P = 0.063) or during maximal contraction (P = 0.392), or between the experimental and control groups at rest (P = 0.392) or during maximum contraction (P = 0.259). The muscle thickness in the experimental group differed significantly over time. CONCLUSIONS: Botulinum toxin injection only changes the muscle thickness and does not affect the subcutaneous thickness from the skin surface to the masseter muscle.


Assuntos
Toxinas Botulínicas Tipo A/administração & dosagem , Hipertrofia/tratamento farmacológico , Músculo Masseter/anormalidades , Fármacos Neuromusculares/administração & dosagem , Tela Subcutânea/efeitos dos fármacos , Adulto , Toxinas Botulínicas Tipo A/efeitos adversos , Feminino , Humanos , Hipertrofia/patologia , Injeções Intramusculares/efeitos adversos , Masculino , Músculo Masseter/diagnóstico por imagem , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/patologia , Fármacos Neuromusculares/efeitos adversos , Fatores Sexuais , Tela Subcutânea/anatomia & histologia , Tela Subcutânea/diagnóstico por imagem , Ultrassonografia , Adulto Jovem
12.
Muscle Nerve ; 56(4): 804-813, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-28026014

RESUMO

INTRODUCTION: To better understand the pathophysiology of chronic muscle pain, there are multiple animal models that mimic different acute/chronic pain conditions, such as carrageenan injection. Our previous studies demonstrated differences between muscles of different innervation in acute pain. In this study we characterized the effect of carrageenan in 2 muscles: masseter (trigeminal innervation) and gastrocnemius (spinal innervation). METHODS: Carrageenan (3%, 6%, and 9%) was injected into the masseter and gastrocnemius of rats. Mechanical, heat, and chemical nociceptive thresholds were measured for 14 days. RESULTS: Carrageenan did not induce mechanical allodynia or thermal hypersensitivity in either muscle. Instead, it induced a short-lasting mechanical hyperalgesia, greater in the masseter than in the gastrocnemius. CONCLUSION: Carrageenan injected into the masseter and gastrocnemius induces a short-lasting hyperalgesia. These results could indicate a higher susceptibility of orofacial muscles to this type of insult and, consequently, a difference between trigeminal and spinal innervation. Muscle Nerve 56: 804-813, 2017.


Assuntos
Carragenina/toxicidade , Hiperalgesia/induzido quimicamente , Músculo Masseter/efeitos dos fármacos , Músculo Esquelético/efeitos dos fármacos , Medição da Dor/efeitos dos fármacos , Animais , Carragenina/administração & dosagem , Hiperalgesia/patologia , Injeções Intramusculares , Masculino , Músculo Masseter/patologia , Músculo Esquelético/patologia , Medição da Dor/métodos , Ratos , Ratos Wistar , Resultado do Tratamento
13.
Eur J Oral Sci ; 125(6): 453-462, 2017 12.
Artigo em Inglês | MEDLINE | ID: mdl-29105170

RESUMO

This study aimed to investigate the effect of glutamate-evoked masseter muscle pain on intramuscular oxygenation during rest and sustained elevated muscle activity (SEMA). Seventeen healthy individuals participated in two sessions in which they were injected with glutamate and saline in random order. Each session was divided into three, 10-min periods. During the first (period 1) and the last (period 3) 10-min periods, participants performed five intercalated 1-min bouts of masseter SEMA with 1-min periods of 'rest'. At onset of the second 10-min period, glutamate (0.5 ml, 1 M; Ajinomoto, Tokyo, Japan) or isotonic saline (0.5 ml; 0.9%) was injected into the masseter muscle and the participants kept the muscle relaxed in a resting position for 10 min (period 2). The hemodynamic characteristics of the masseter muscle were recorded simultaneously during the experiment by a laser blood-oxygenation monitor. The results demonstrated that glutamate injections caused significant levels of self-reported pain in the masseter muscle; however, this nociceptive input did not have robust effects on intramuscular oxygenation during rest or SEMA tasks. Interestingly, these findings suggest an uncoupling between acute nociceptive activity and hemodynamic parameters in both resting and low-level active jaw muscles. Further studies are needed to explore the pathophysiological significance of blood-flow changes for persistent jaw-muscle pain conditions.


Assuntos
Ácido Glutâmico/farmacologia , Músculo Masseter/efeitos dos fármacos , Músculo Masseter/metabolismo , Contração Muscular/efeitos dos fármacos , Oxigênio/sangue , Adulto , Feminino , Voluntários Saudáveis , Hemodinâmica , Humanos , Masculino , Medição da Dor , Limiar da Dor
14.
J Oral Maxillofac Surg ; 75(6): 1257-1262, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28157491

RESUMO

PURPOSE: Dexamethasone seems to suppress postoperative swelling. However, the standard administration dose of dexamethasone for bilateral sagittal split osteotomy (BSSO) has not been reported. This study focused on clarifying the most effective dose of dexamethasone for BSSO. MATERIALS AND METHODS: This research was planned as a prospective, randomized controlled, double-blind study. Patients undergoing BSSO were randomly assigned to receive intravenous preoperative dexamethasone under 3 different dose conditions: 16 mg, 8 mg, and 0 mg (control). The endpoints of this study were 1) postoperative changes in masseter muscle thickness and buccal soft tissue thickness; 2) postoperative changes in maximum incisal opening; 3) postoperative changes in sensation of the chin and lower lip region; 4) postoperative changes in blood examination findings (white blood cell count, neutrophil count, C-reactive protein level, and lymphocyte count); and 5) types of complications. Data were recorded at 2 to 4 time intervals: before surgery, postoperative day 1, postoperative day 2, and postoperative day 3. Average age, gender, average body mass index, average surgery time, and average blood loss also were examined. Data were analyzed by 1-way analysis of variance (Bonferroni multiple-comparisons test) after the Bartlett test. RESULTS: We enrolled 24 patients, including 5 men and 19 women, in this study. The rate of increase in the thickness of the masseter muscle 24 hours after BSSO was 38.4% in the 16-mg group (n = 8), 57.7% in the 8-mg group (n = 8), and 56.1% in the 0-mg group (n = 8). The rate of increase in masseter muscle thickness in the 16-mg group was significantly lower than that in the 0-mg group (P < .05). Regarding the number of lymphocytes after surgery, the 16-mg and 8-mg groups maintained preoperative levels whereas there was a reduced number of lymphocytes in the control group. No statistically significant results were obtained for the following study endpoints: postoperative changes in maximum incisal opening and postoperative changes in sensation of the chin and lower lip region. CONCLUSIONS: This investigation showed that the most effective dose of dexamethasone for BSSO is 16 mg.


Assuntos
Anti-Inflamatórios/administração & dosagem , Dexametasona/administração & dosagem , Edema/prevenção & controle , Músculo Masseter/efeitos dos fármacos , Osteotomia Sagital do Ramo Mandibular , Complicações Pós-Operatórias/prevenção & controle , Adulto , Método Duplo-Cego , Feminino , Humanos , Infusões Intravenosas , Masculino , Procedimentos Cirúrgicos Ortognáticos , Cuidados Pré-Operatórios , Estudos Prospectivos , Tomografia Computadorizada por Raios X , Resultado do Tratamento
15.
Clin Oral Investig ; 21(3): 727-734, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28255752

RESUMO

OBJECTIVE: The objective of the study was to conduct a systematic review of the literature assessing the effects of botulinum toxin (BoNT-A) injections in the management of bruxism. MATERIALS AND METHODS: Search for articles involved the PubMed, Scopus, Web of Science, Embase, Cochrane, Scielo and Lilacs databases. Specific terms were used and the search carried out from 1980 to March 2016 by three independent researchers. Randomized controlled studies (RCTs), prospective and before-after studies that applied BoNT-A at the masseter and/or temporalis muscles were included. RESULTS: Three RCTs and two uncontrolled before-after studies out of 904 identified citations were included in this review. All five articles dealt with sleep bruxism and featured a small sample size. None of them was about awake bruxism. Two randomized clinical trials were double-blinded, with a control group using saline solution. Two studies used polysomnography/electromyography for sleep bruxism diagnosis, whilst others were based on history taking and clinical examination. All studies using subjective evaluations for pain and jaw stiffness showed positive results for the BoNT-A treatment. In contrast, the two studies using objective evaluations did not demonstrate any reduction in bruxism episodes, but a decrease in the intensity of muscles contractions. CONCLUSION: Despite the paucity of works on the topic, BoNT-A seems to be a possible management option for sleep bruxism, minimizing symptoms and reducing the intensity of muscle contractions, although further studies are necessary especially as far as the treatment indications for bruxism itself is concerned. CLINICAL RELEVANCE: BoNT-A has been increasingly diffused in dentistry over recent years, being also used for pain management in patients with bruxism. Nonetheless, there is no consensus about its effects in this disorder.


Assuntos
Toxinas Botulínicas Tipo A/uso terapêutico , Bruxismo/tratamento farmacológico , Fármacos Neuromusculares/uso terapêutico , Toxinas Botulínicas Tipo A/administração & dosagem , Eletromiografia , Humanos , Injeções , Músculo Masseter/efeitos dos fármacos , Fármacos Neuromusculares/administração & dosagem , Polissonografia , Músculo Temporal/efeitos dos fármacos
16.
J Craniofac Surg ; 28(4): e392-e395, 2017 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-28590396

RESUMO

PURPOSE: The objective of this study was to evaluate whether silk fibroin (SF) incorporated into 4-hexylresorcinol (4HR) could increase botulinum toxin-A (BTX-A) activity. MATERIAL AND METHODS: In total, 30 rats were used for this study. The animals were divided into 6 groups according to the injected materials (SA: saline only; SF; 4HR; B2: 2 units of BTX-A; B2 + SF + 4HR: combination of B2, SF, and 4HR; B5: 5 units of BTX-A). Serial sonography was used for the evaluation of muscle thickness after injection. Immunohistochemical staining was used for the evaluation of myosin type II (myo2) and Bcl-2 protein expression. RESULTS: The relative thickness of the masseter muscle in B2 group was 66.14% ±â€Š4.55% to the preinjection level; in B2 + SF + 4HR group was 54.59% ±â€Š4.83%, and in B5 group was 56.19% ±â€Š8.28%. Any BTX-injected group showed significantly lower value of the relative muscle thickness compared to SA, SF, or 4HR group (P < 0.001 for all). The difference of relative muscle thickness between B2 group and B2 + SF + 4HR group was statistically significant (P < 0.001). The intensity of myo2 immunostaining in B5, B2, and B2 + SF + 4HR group was significantly higher than those in the other groups (P < 0.05). CONCLUSIONS: When 2 units of BTX was incorporated to SF and 4HR, combination formula showed similar activity to those of 5 units of BTX.


Assuntos
Anti-Helmínticos/administração & dosagem , Toxinas Botulínicas Tipo A/administração & dosagem , Fibroínas/administração & dosagem , Hexilresorcinol/administração & dosagem , Músculo Masseter/efeitos dos fármacos , Fármacos Neuromusculares/administração & dosagem , Animais , Injeções Intramusculares , Músculo Masseter/patologia , Ratos
17.
Acta Anaesthesiol Scand ; 60(6): 734-46, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26899676

RESUMO

BACKGROUND: The aim of this study was to characterize the dose-effect relationship of rocuronium at the adductor pollicis and masseter muscles. METHODS: Ten, ASA I, adult patients, received a bolus dose of rocuronium 0.3 mg/kg during propofol based anesthesia. Train-of-four (TOF) was simultaneously monitored at the masseter and the adductor pollicis muscles until recovery. Rocuronium arterial serum concentrations were measured during 120 min. The first twitch of the TOF response was used to characterize the time-effect profile of both muscles using pharmacokinetic-pharmacodynamic analysis in NONMEM. A decrease in NONMEM objective function (∆OFV) of 3.84 points for an added parameter was considered significant at the 0.05 level. RESULTS: Onset time at the masseter (mean ± SD, 1.5 ± 0.9 min) was faster than at the adductor pollicis (2.7 ± 1.4 min, P < 0.05). Recovery, measured as the time to TOF ratio = 0.9 was similar between muscles 29.9 ± 6.7 (adductor pollicis) vs. 29.3 ± 8.1 (masseter). (P = 0.77). The estimated pharmacodynamic parameters [mean (95% CI)] of the adductor pollicis muscle and the masseter muscle were; plasma effect-site equilibration half-time (teq) 3.25 (2.34, 3.69) min vs. 2.86 (1.83, 3.29) min, (∆OFV 383.665); Ce50 of 1.24 (1.13, 1.56) mg/l vs. 1.19 (1.00, 1.21) mg/l, (∆OFV 184.284); Hill coefficient of 3.97 (3.82, 5.62) vs. 4.68 (3.83, 5.71), (∆OFV 78.906). CONCLUSIONS: We found that the masseter muscle has faster onset of blockade and similar recovery profile than adductor pollicis muscle. These findings were best, explained by a faster plasma effect-site equilibration of the masseter muscle to rocuronium.


Assuntos
Músculo Masseter/efeitos dos fármacos , Fármacos Neuromusculares não Despolarizantes/farmacocinética , Androstanóis/farmacocinética , Anestesia , Mãos , Humanos , Músculo Esquelético/efeitos dos fármacos
18.
Aesthet Surg J ; 36(10): 1093-1100, 2016 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-27193172

RESUMO

BACKGROUND: Lower face aesthetic contouring is in high demand among Asians with wide and short faces desiring a slim lower face. For this purpose invasive mandible angle reduction and genioplasty are complex procedures with significant risks and downtime. Non-invasive botulinum toxin A injection into bilateral masseters - while popular for lower face contouring - does not address facial length deficiency in wide and short faces. Autologous chin fat grafting is a simple minimally-invasive technique for facial lengthening. OBJECTIVES: We present our experience pairing chin fat grafting and masseteric botulinum toxin injection for effective lower face contouring. METHODS: Thirteen consecutive patients with relatively wide and short faces underwent chin fat grafting and 1 to 3 serial masseteric botulinum toxin A injections. Mean follow up after final intervention was 20 months (range, 6 months to 3 years). RESULTS: The postoperative mean ratio of bigonial distance to total facial height improved from 0.599 to 0.569 (P < .01), closer to the ideal ratio of 0.561. The mean ratio of upper lip length to lower lip and chin length improved from 0.611 to 0.560 (P < .01), nearing the ideal 0.542. Postoperative lateral profile in all was ideal. There were no complications at follow up. Results were durable at latest follow up and most were satisfied with their final appearance. CONCLUSIONS: Combined tridimensional chin fat grafting and botulinum toxin masseteric injection is an effective, simple, fast, inexpensive, safe, and minimally-invasive strategy for aesthetic lower face contouring of short and wide faces, with short downtime, long-lasting results, and high patient satisfaction. LEVEL OF EVIDENCE: 4 Therapeutic.


Assuntos
Inibidores da Liberação da Acetilcolina/administração & dosagem , Tecido Adiposo/transplante , Toxinas Botulínicas/administração & dosagem , Queixo/cirurgia , Técnicas Cosméticas , Estética , Músculo Masseter/efeitos dos fármacos , Procedimentos de Cirurgia Plástica/métodos , Adulto , Pontos de Referência Anatômicos , Feminino , Humanos , Injeções Intramusculares , Pessoa de Meia-Idade , Satisfação do Paciente , Estudos Retrospectivos , Fatores de Tempo , Transplante Autólogo , Resultado do Tratamento , Adulto Jovem
19.
J Headache Pain ; 17: 29, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27011213

RESUMO

BACKGROUND: Temporomandibular joint dysfunction are often accompanied by symptoms of headache such as tension-type headache which is the most frequent spontaneous primary headache. Masseter muscle pain is commonly reported in this group. The purpose of the study was to assess the efficiency of intramuscular botulinum toxin type A injections for treating masseter muscle pain in patients with temporomandibular joint dysfunction and tension-type headache. METHODS: This prospective outcome study consisted of 42 subjects of both genders aged 19-48 years diagnosed with masseter muscle pain related to temporomandibular joint dysfunction and tension-type headache. The subjects were treated by the intramuscular injection of 21 U (mice units) of botulinum toxin type A (Botox, Allergan) in the area of the greatest cross-section surface of both masseter bellies. Pain intensity was evaluated using visual analogue scale (VAS) and verbal numerical rating scale (VNRS) 1 week before the treatment and 24 weeks after the treatment. The obtained data were analyzed using the Wilcoxon matched pairs test (p ≤ 0,005). RESULTS: The results of this study showed a decrease in the number of referred pain episodes including a decrease in pain in the temporal region bilaterally, a reduction of analgesic drugs intake as well as a decrease in reported values of VAS and VNRS after injections (p = 0,000). CONCLUSIONS: The intramuscular botulinum toxin type A injections have been an efficient method of treatment for masseter muscle pain in patients with temporomandibular joint dysfunction and tension-type headache.


Assuntos
Toxinas Botulínicas Tipo A/uso terapêutico , Mialgia/tratamento farmacológico , Fármacos Neuromusculares/uso terapêutico , Síndrome da Disfunção da Articulação Temporomandibular/tratamento farmacológico , Cefaleia do Tipo Tensional/tratamento farmacológico , Adulto , Toxinas Botulínicas Tipo A/farmacologia , Feminino , Humanos , Injeções Intramusculares , Masculino , Músculo Masseter/efeitos dos fármacos , Pessoa de Meia-Idade , Fármacos Neuromusculares/farmacologia , Medição da Dor , Estudos Prospectivos , Resultado do Tratamento , Adulto Jovem
20.
Muscle Nerve ; 52(1): 88-93, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-26039454

RESUMO

INTRODUCTION: Pigs respond to direct administration of botulinum neurotoxins (BoNTs), although they are resistant to botulism. The human masseter is frequently targeted for BoNT therapy. We aimed to understand how BoNT affects chewing by injecting porcine masseters. METHODS: One masseter of minipigs was injected with BoNT serotype A or B at doses comparable to those used in humans. Masticatory function was evaluated electromyographically. Muscle force was measured during tetany. Four weeks after injection, strain gauges affixed to the mandible assessed bone strain during chewing. Masseter mass and fiber diameter were measured after euthanasia. RESULTS: BoNT-A had no measurable effect. In contrast, BoNT-B reduced electrical activity and muscle force, producing substantial asymmetry between injected and uninjected muscles. CONCLUSIONS: The pig masseter is highly resistant to direct injection of BoNT-A, but it is affected by BoNT-B.


Assuntos
Toxinas Botulínicas Tipo A/farmacologia , Músculo Masseter/efeitos dos fármacos , Fármacos Neuromusculares/farmacologia , Animais , Eletromiografia , Potencial Evocado Motor/efeitos dos fármacos , Feminino , Lateralidade Funcional , Estatísticas não Paramétricas , Suínos , Fatores de Tempo
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