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1.
Pediatr Neonatol ; 65(2): 145-151, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37684161

RESUMO

BACKGROUND: Group B Streptococci (GBS) are common vaginal bacteria found in 20-30% of pregnant women and a significant cause of invasive infections in newborns. Recently, attention has been focused on the efficacy of probiotics during the perinatal period. However, the effect of probiotic intake on the mother-to-child transmission (MTCT) of GBS remains unknown. METHODS: Pregnant women with positive GBS results from vaginal and rectal swab cultures at 35-37 weeks of gestation were randomly assigned to the probiotic group or the control group in an open-label manner at the Department of Obstetrics and Gynecology, San-ikukai Hospital, Tokyo, Japan. The probiotic group received Lactobacillus reuteri during antenatal checkups from 35 to 37-week gestation to 1 month after delivery. Rectal swabs were obtained from the newborns at 5 days and at 1 month of age. Whole-genome sequencing was performed to test for GBS strains in the mother, whose newborn carried GBS at the 1-month checkup. Multi-locus sequence typing and single nucleotide polymorphism analyses were performed to identify MTCT. RESULTS: Overall, 67 mother-infant pairs were included, with 31 in the probiotic group and 36 in the control group. The positivity rate of GBS in newborns at 1 month of age was 10% (n = 3) in the probiotic group and 28% (n = 10) in the control group. In newborns carrying GBS at 1 month of age, genetic analysis revealed that the MTCT rate was 6% in the probiotic group and 22% in the control group, although the difference was not statistically significant (p = 0.0927). CONCLUSION: No statistically significant difference was found; however, the consumption of L. reuteri by women with GBS-positive pregnancies may inhibit the MTCT of GBS.


Assuntos
Complicações Infecciosas na Gravidez , Probióticos , Infecções Estreptocócicas , Gravidez , Feminino , Recém-Nascido , Humanos , Mães , Transmissão Vertical de Doenças Infecciosas/prevenção & controle , Estudos Prospectivos , Tipagem de Sequências Multilocus , Infecções Estreptocócicas/prevenção & controle , Streptococcus agalactiae , Probióticos/uso terapêutico
2.
Ophthalmologica ; 241(3): 161-169, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-30176671

RESUMO

PURPOSE: To assess the efficacy and safety of sub-Tenon injection of triamcinolone acetonide (WP-0508ST) for the patients with diabetic macular edema (DME). METHODS: This multicenter, randomized, double-masked, comparative, controlled study was performed in 95 patients with DME. The patients were randomly divided into 20 mg WP-0508ST, 40 mg WP-0508ST, and control groups. RESULTS: A significant improvement in central macular thickness (CMT) was observed (p < 0.001) at 12 weeks after a single sub-Tenon injection of 20 mg WP-0508ST. The 40 mg group also demonstrated improvement in CMT, but the difference was not significant. In addition, the best-corrected visual acuity was improved in both the 20 mg and 40 mg groups at 12 weeks. The major side effects were increased intraocular pressure (9.4% in the 20 mg group and 13.3% in the 40 mg group) and lenticular opacity (6.3% in the 20 mg group and 10.0% in the 40 mg group). However, none of the patients with increased intraocular pressure required surgery. CONCLUSION: The efficacy and tolerability of WP-0508ST in the treatment of DME were confirmed, and 20 mg was determined to be the optimal dose.


Assuntos
Retinopatia Diabética/tratamento farmacológico , Angiofluoresceinografia/métodos , Edema Macular/tratamento farmacológico , Tomografia de Coerência Óptica/métodos , Triancinolona Acetonida/administração & dosagem , Acuidade Visual , Adulto , Idoso , Retinopatia Diabética/complicações , Retinopatia Diabética/diagnóstico , Relação Dose-Resposta a Droga , Método Duplo-Cego , Feminino , Seguimentos , Fundo de Olho , Glucocorticoides/administração & dosagem , Humanos , Injeções Intraoculares , Edema Macular/diagnóstico , Edema Macular/etiologia , Masculino , Pessoa de Meia-Idade , Cápsula de Tenon , Fatores de Tempo , Resultado do Tratamento
3.
J Histochem Cytochem ; 53(6): 735-44, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15928322

RESUMO

In rat lung, the definitive alveoli are established during development by the outgrowth of secondary septa from the primary septa present in newborn; however, the mechanism of alveolar formation has not yet been fully clarified. In this study, we characterize the septal interstitial cells in developing alveoli. During the perinatal period, alpha-SMA-containing slender cells were found in the primitive alveolar septa. Alpha-SMA-containing cells were detected at the tips of the septa until postnatal day 21, when the alveolar formation was almost completed, but disappeared in adult. Immunoelectron microscopy demonstrated that alpha-SMA is localized mainly in the cellular protrusions, which are connected with the elastic fibers around the interstitial cells. Developmentally regulated brain protein (drebrin) is also located in the cell extensions containing alpha-SMA in immature alveolar interstitial cells. In adult lung, alpha-SMA-positive cells are located only at the alveolar ducts but are not found in the secondary septa. Desmin is expressed only in alpha-SMA-containing cells at the alveolar ducts but not in those at the tip of alveolar septa. These results suggest that a part of the septal interstitial cells are temporarily alpha-SMA- and drebrin-positive during maturation. Alpha-SMA- and drebrin-containing septal interstitial cells (termed septal myofibroblast-like cells) may play an important role in alveolar formation.


Assuntos
Actinas/biossíntese , Proteínas de Filamentos Intermediários/biossíntese , Neuropeptídeos/biossíntese , Alvéolos Pulmonares/metabolismo , Animais , Animais Recém-Nascidos , Fibroblastos/metabolismo , Fibroblastos/ultraestrutura , Imuno-Histoquímica , Técnicas In Vitro , Microscopia Imunoeletrônica , Alvéolos Pulmonares/embriologia , Alvéolos Pulmonares/crescimento & desenvolvimento , Ratos , Ratos Wistar
4.
J Ocul Pharmacol Ther ; 19(6): 569-77, 2003 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-14733714

RESUMO

The effects of nonsteroidal anti-inflammatory drugs (NSAIDs) on experimental allergic conjunctivitis, induced by ocular challenge with antigen in actively sensitized guinea pigs, were investigated. NSAIDs reduced the increase in prostaglandin D2 (PGD2) and E2 (PGE2) in the ocular lavage fluid. The inhibition of NSAIDs to these increases was approximately 90%-95%. NSAIDs also lowered itch-scratch response (ISR) to approximately one-third to one-half of the vehicle-treated group. However, these drugs scarcely affected plasma exudation in the conjunctiva. Ketotifen, an H1 histamine receptor antagonist, inhibited both pathophysiological changes (inhibition: 70%-80%). However, this drug was less efficacious than NSAIDs in reducing PGD2 and PGE2 levels. Moreover, topical administration of histamine induced ISR and plasma exudation; in contrast, PGD2 induced ISR exclusively. These results suggest that a part of antigen-induced ISR may be attributable to PGs. However, PGs may not play a key role in plasma exudation; other mediators such as histamine may be involved.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Conjuntivite Alérgica/tratamento farmacológico , Modelos Animais de Doenças , Administração Tópica , Animais , Anti-Inflamatórios não Esteroides/administração & dosagem , Anti-Inflamatórios não Esteroides/farmacologia , Antígenos/administração & dosagem , Antígenos/efeitos adversos , Benzofenonas/farmacocinética , Benzopiranos/administração & dosagem , Benzopiranos/farmacocinética , Bromobenzenos/farmacocinética , Conjuntivite Alérgica/etiologia , Diclofenaco/administração & dosagem , Diclofenaco/farmacocinética , Dinoprostona/antagonistas & inibidores , Dinoprostona/química , Dinoprostona/metabolismo , Azul Evans , Exsudatos e Transudatos/química , Olho/efeitos dos fármacos , Cobaias , Histamina/administração & dosagem , Histamina/efeitos adversos , Liberação de Histamina/efeitos dos fármacos , Imunização , Injeções Intraperitoneais , Injeções Subcutâneas , Cetotifeno/administração & dosagem , Cetotifeno/farmacocinética , Cetotifeno/uso terapêutico , Masculino , Ovalbumina/administração & dosagem , Ovalbumina/farmacologia , Propionatos/administração & dosagem , Propionatos/farmacocinética , Prostaglandina D2/antagonistas & inibidores , Prostaglandina D2/química , Prostaglandina D2/metabolismo , Prurido/induzido quimicamente , Prurido/prevenção & controle , Irrigação Terapêutica/métodos
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