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1.
Neural Regen Res ; 18(2): 244-252, 2023 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-35900398

RESUMEN

Subarachnoid hemorrhage (SAH) is a dominant cause of death and disability worldwide. A sharp increase in intracranial pressure after SAH leads to a reduction in cerebral perfusion and insufficient blood supply for neurons, which subsequently promotes a series of pathophysiological responses leading to neuronal death. Many previous experimental studies have reported that excitotoxicity, mitochondrial death pathways, the release of free radicals, protein misfolding, apoptosis, necrosis, autophagy, and inflammation are involved solely or in combination in this disorder. Among them, irreversible neuronal apoptosis plays a key role in both short- and long-term prognoses after SAH. Neuronal apoptosis occurs through multiple pathways including extrinsic, mitochondrial, endoplasmic reticulum, p53 and oxidative stress. Meanwhile, a large number of blood contents enter the subarachnoid space after SAH, and the secondary metabolites, including oxygenated hemoglobin and heme, further aggravate the destruction of the blood-brain barrier and vasogenic and cytotoxic brain edema, causing early brain injury and delayed cerebral ischemia, and ultimately increasing neuronal apoptosis. Even there is no clear and effective therapeutic strategy for SAH thus far, but by understanding apoptosis, we might excavate new ideas and approaches, as targeting the upstream and downstream molecules of apoptosis-related pathways shows promise in the treatment of SAH. In this review, we summarize the existing evidence on molecules and related drugs or molecules involved in the apoptotic pathway after SAH, which provides a possible target or new strategy for the treatment of SAH.

2.
BMJ Open ; 12(6): e056400, 2022 06 10.
Artículo en Inglés | MEDLINE | ID: mdl-35688599

RESUMEN

OBJECTIVE: The Grades of Recommendations, Assessment, Development and Evaluation working group recently developed an innovative approach to interpreting results from network meta-analyses (NMA) through minimally and partially contextualised methods; however, the optimal method for presenting results for multiple outcomes using this approach remains uncertain. We; therefore, developed and iteratively modified a presentation method that effectively summarises NMA results of multiple outcomes for clinicians using this new interpretation approach. DESIGN: Qualitative descriptive study. SETTING: A steering group of seven individuals with experience in NMA and design validation studies developed two colour-coded presentation formats for evaluation. Through an iterative process, we assessed the validity of both formats to maximise their clarity and ease of interpretation. PARTICIPANTS: 26 participants including 20 clinicians who routinely provide patient care, 3 research staff/research methodologists and 3 residents. MAIN OUTCOME MEASURES: Two team members used qualitative content analysis to independently analyse transcripts of all interviews. The steering group reviewed the analyses and responded with serial modifications of the presentation format. RESULTS: To ensure that readers could easily discern the benefits and safety of each included treatment across all assessed outcomes, participants primarily focused on simple information presentations, with intuitive organisational decisions and colour coding. Feedback ultimately resulted in two presentation versions, each preferred by a substantial group of participants, and development of a legend to facilitate interpretation. CONCLUSION: Iterative design validation facilitated the development of two novel formats for presenting minimally or partially contextualised NMA results for multiple outcomes. These presentation approaches appeal to audiences that include clinicians with limited familiarity with NMAs.


Asunto(s)
Proyectos de Investigación , Humanos , Metaanálisis en Red , Investigación Cualitativa
3.
Int J Biol Markers ; 35(1): 41-46, 2020 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-31992114

RESUMEN

OBJECTIVE: α-fetoprotein (AFP) expression is activated during the embryonic stage or hepatocellular carcinogenesis, so it is presumed that AFP is a key endogenous molecule to promote cell proliferation or differentiation. We carried out gene screening in an unknown family with hyper-alpha-fetoproteinemia and some sporadic menopausal women, and discussed the relationship between AFP expression and liver cirrhosis. METHODS: Peripheral blood samples from family members, patients with malignant liver tumors, and normal controls were collected. Full-length sequence of AFP was amplified and directly sequenced, and compared with normal controls. HNF-1α and HNF-1ß in plasma levels of family members, patients with liver cancer, newborns, pregnant women, and normal subjects were detected by ELISA, and the relationship between HNF-1 and AFP mutation or high expression was evaluated. RESULTS: There was a mutation in AFP promoter region at c.-200 C>T, which was located at the binding site of AFP hepatocyte nuclear factor 1 (HNF-1). AFP was higher than 4000 ng/L in all members carrying the mutation, but liver cancer was excluded in the family with hyper-alpha-fetoprotein. However, cirrhosis occurred in post-menopausal women. The cases reviewed showed that unknown hyper-alpha-fetoprotein was closely related to HNF-1 binding point of AFP in post-menopausal women with cirrhosis (7/11), while the plasma levels of HNF-1α and HNF-1ß were not significantly different. CONCLUSION: The mutation of the HNF-1 binding point of AFP may lead to an abnormal high expression of AFP by altering the binding of HNF transcription factors, which is closely related to cirrhosis in menopausal women.


Asunto(s)
Factor Nuclear 1 del Hepatocito/genética , Cirrosis Hepática/genética , Mutación Puntual , alfa-Fetoproteínas/genética , Adulto , Femenino , Factor Nuclear 1 del Hepatocito/sangre , Humanos , Cirrosis Hepática/sangre , Neoplasias Hepáticas/sangre , Neoplasias Hepáticas/genética , Masculino , Persona de Mediana Edad , Linaje , Posmenopausia , Regiones Promotoras Genéticas , Estudios Retrospectivos , alfa-Fetoproteínas/metabolismo
4.
Zhonghua Nan Ke Xue ; 12(9): 800-2, 2006 Sep.
Artículo en Chino | MEDLINE | ID: mdl-17009531

RESUMEN

OBJECTIVE: To assess an integrated method of operation + Chinese medicine + dexamethasone + vitamin E in treating varicocele. METHODS: Ninety-six patients with varicocele were randomly divided into two groups, the experimental group (Group A, n=47) treated with the integrated method, the control group (Group B, n=49) treated with Chinese medicine, dexamethasone and vitamin E. RESULTS: After the treatment, the sperm density and motility and pregnancy rate were higher (P < 0.01 or P < 0.05) and the sperm deformity rate was lower in the experiment group than in the control (P < 0.05). CONCLUSION: The integrated method works better than either operation or Chinese medicine applied alone in the treatment of varicocele.


Asunto(s)
Dexametasona/uso terapéutico , Medicamentos Herbarios Chinos/uso terapéutico , Fitoterapia , Varicocele/tratamiento farmacológico , Vitamina E/uso terapéutico , Adulto , Terapia Combinada , Femenino , Humanos , Infertilidad Masculina/etiología , Infertilidad Masculina/terapia , Masculino , Persona de Mediana Edad , Embarazo , Índice de Embarazo , Recuento de Espermatozoides , Varicocele/cirugía
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