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1.
Clinics ; 74: e573, 2019. tab, graf
Article Dans Anglais | LILACS | ID: biblio-1001827

Résumé

OBJECTIVES: The pedunculopontine nucleus (PPN) is considered a promising new target for neurostimulation in Parkinson's disease (PD) patients with postural instability and gait disturbance that is refractory to other treatment modalities. However, the PPN is typically difficult to visualize with magnetic resonance imaging (MRI) at clinical field strengths, which greatly limits the PPN as a viable surgical target for deep brain stimulation (DBS). Thus, the aim of this study is to directly visualize the PPN based on 7.0T ultrahigh-field MRI. METHODS: Five PD patients were enrolled and scanned using the MP2RAGE sequence on a 7.0T ultrahigh-field MRI scanner. Then, the MP2RAGE sequences were imported into a commercially available navigation system. The coordinates of the directly localized PPN poles were recorded in the navigation system relative to the anterior commissure-posterior commissure plane. RESULTS: Our results indicated that the PPN presented intermediate signal intensity in the 7.0T ultrahigh-field MR images in comparison with the surrounding structure, such as the hypo-intensity of the periaqueductal gray and the hyperintensity of the neighboring white matter tracts, in PD patients. The mean coordinates for the rostral and caudal poles of PPN were 6.50 mm and 7.20 mm lateral, 1.58 mm and 2.21 mm posterior, and 8.89 mm and 13.83 mm relative to the posterior commissure. CONCLUSION: Our findings provide, for the first time, direct visualization of the PPN using the MP2RAGE sequence on a 7.0T ultrahigh-field MRI, which may improve the accuracy of stereotactic targeting of the PPN and improve the outcomes in patients undergoing DBS.


Sujets)
Humains , Mâle , Femelle , Adulte , Adulte d'âge moyen , Maladie de Parkinson/imagerie diagnostique , Imagerie par résonance magnétique/méthodes , Amélioration d'image/instrumentation , Noyau tegmental pédonculopontin/imagerie diagnostique , Traitement d'image par ordinateur/instrumentation , Traitement d'image par ordinateur/méthodes , Imagerie par résonance magnétique/instrumentation , Amélioration d'image/méthodes , Techniques stéréotaxiques/instrumentation , Exactitude des données
2.
Journal of Experimental Hematology ; (6): 793-796, 2009.
Article Dans Chinois | WPRIM | ID: wpr-334023

Résumé

Limitations of polyacrylamide gel or agarose gel electrophoretic methods in genotyping research affect the interpreting of detection results. In order to develop a simple and reliable method for appraising results of ABO genotyping detection, the microfluidic chip analysis system was established by using microfluidic chip to replace the gel electrophoresis and combining with multiplex-PCR-RFLP technique. 150 blood samples were tested by this microfluidic chip analysis system with multiplex-PCR-RFLP technique to evaluate its stability and accuracy. The results showed that all the testing results were consistent with serologic ABO genotyping results and 1 blood sample with decrease of B antigen caused by CML was identified. In conclusion, the established microfluidic chip analysis system is stable and reliable technique. Application of this technique enables the ABO genotyping results to be more objective and accurate.


Sujets)
Humains , Système ABO de groupes sanguins , Génétique , Groupage sanguin et épreuve de compatibilité croisée , Méthodes , Amorces ADN , Génétique , Génotype , Techniques d'analyse microfluidique , Microfluidique , Séquençage par oligonucléotides en batterie
3.
Journal of Experimental Hematology ; (6): 425-428, 2008.
Article Dans Chinois | WPRIM | ID: wpr-253305

Résumé

The aim of this study was to establish a diagnostic method for ABO genotyping and to investigate the distribution of ABO genotype in Beijing Han population so as to understand the distribution characteristics and regularity of ABO genotype. An ABO genotyping method was established by using multiplex-PCR-RFLP and PCR-SSP techniques, and the ABO allele frequency in Beijing Han population was investigated. The results showed that A102, O1 and B allele were more common genes in Beijing Han individuals. And A102 allele was predominant in the phenotype A group in this population. Three O2 alleles were found and no A201 allele was found while gene frequency investigation was performed. No A101A101, A101O2, A102O2, BO2 and O2O2 in this population were discovered. It is concluded that the primary regularity of ABO allele distribution in Beijing Han population is found through this study. It provides basic reference for further study of ABO types.


Sujets)
Adulte , Femelle , Humains , Mâle , Adulte d'âge moyen , Jeune adulte , Système ABO de groupes sanguins , Génétique , Allèles , Asiatiques , Génétique , Chine , Ethnologie , Fréquence d'allèle , Génotype , Réaction de polymérisation en chaîne , Méthodes , Polymorphisme génétique
4.
Journal of Experimental Hematology ; (6): 332-337, 2005.
Article Dans Chinois | WPRIM | ID: wpr-356564

Résumé

Erythropoietin (EPO) is an acidic glycoprotein that was first detected as a hematopoietic factor and its synthesis is triggered in response to cellular hypoxia-sensing. EPO binds to type I cytokine receptors, which associate with the non-receptor tyrosine kinase Jak2, and thereby activate Stat 5a/5b, Ras/MAPK, and PI3-K/Akt signaling pathways. The recent discovery shows that there is a specific EPO/EPO-receptor system in the central nervous system (CNS), independently of the haematopoietic system. Hypoxia and anemia can up-regulate EPO/EPOR expressions in the CNS. Further studies demonstrate that EPO has substantial neuro-protective effects and acts as a neurotrophic factor on central cholinergic neurons, influencing their differentiation and regeneration. EPO also exerts neuro-protective activities in different models of brain damage in vivo and in vitro, such as hypoxia, cerebral ischaemia and sub-arachnoid haemorrhage. EPO may also be involved in synaptic plasticity via the inhibition or stimulation of various neurotransmitters. Therefore, human recombinant EPO that activate its receptors in the central nervous system might be utilized in the future clinical practice involving neuroprotection and brain repair.


Sujets)
Animaux , Humains , Encéphale , Métabolisme , Différenciation cellulaire , Érythropoïétine , Métabolisme , Pharmacologie , Neurones , Biologie cellulaire , Neuroprotecteurs , Métabolisme , Pharmacologie , Récepteur érythropoïétine , Métabolisme
5.
Journal of Experimental Hematology ; (6): 353-357, 2005.
Article Dans Chinois | WPRIM | ID: wpr-356560

Résumé

Adult stem cells are the multi-potential cells, which exist in fetal and adult tissues. It can reproduce itself (undergo self-renewal) or give rise to more specialized (differentiated) cells. Under certain inducing conditions, adult stem cells can acquire the ability to differentiate into different tissue cells. Multipotent adult progenitor cells (MAPC), an alternative name of adult stem cell given by Catherine Verfaillie, existing in bone marrow, can differentiate into cells with characteristics of mesodermal, neuroectodermal, and endodermal lineages in vitro at the single-cell level. MAPC can also contribute to most cell types when injected into the blastocyst. Adult stem cell differentiation implies that different cell lineages are derived from a single initial cell; all differentiated cell types are functional in vitro and in vivo; and engraftment is robust and persistent in the physiological and pathological situations. The possible mechanisms may underlie the differentiation: various tissue-specific stem cells are present in different organs; adult stem cells would be reprogrammed when removed from their usual microenvironment and introduced into a different niche that imparts signals to activate a novel genetic program needed for the new cell fate. And true multi-potential stem cells persist in postnatal life. In the future, multi-potent adult stem cells might then be used for therapies of degenerative or genetic disorders of multiple different organs.


Sujets)
Humains , Cellules souches adultes , Biologie cellulaire , Différenciation cellulaire , Cellules souches multipotentes , Biologie cellulaire , Transplantation de cellules souches
6.
Chinese Journal of Applied Physiology ; (6): 345-349, 2003.
Article Dans Chinois | WPRIM | ID: wpr-333755

Résumé

<p><b>AIM</b>To study the effects of hyperthermia on brainstem auditory evoked potentials (BAEP) and middle latency response (MLR) in rats.</p><p><b>METHODS</b>BAEP and MLR were recorded at the skull surface of rats. The body temperature of anesthetized rats increased gradually with a physical method and was detected by a digital thermometer inserted into the rectum. The peak latency (PL), interpeak latency (IPL), wave amplitude and the critical body temperature at which BAEP and MLR completely lost had been observed.</p><p><b>RESULTS</b>All PL and I - II, I - III and I -IV IPL of BAEP shortened more and more as the body temperature increased step by step from 37 degrees C to 41.5 degrees C. But all PL and I - II and I -IV IPL did not shortened further and prolonged a little contrary as the body temperature at 42 degrees C and over 42 degrees C. All PL and P1-P3 and P2-P3 IPL of MLR also shortened as the body temperature increased from 37 degrees C to 43 degrees C. The wave amplitudes of BAEP and MLR decreased as the body temperature increased, especially as the body temperature over 42 degrees C. BAEP and MLR lost completely and synchronously at the body temperature (43.1 +/- 0.5) degrees C, which was not reversed as the body temperature returning to normal by cooling.</p><p><b>CONCLUSION</b>There were obvious effects of hyperthermia on both BAEP and MLR in rats, and irreversible impairments appeared at a critical body temperature.</p>


Sujets)
Animaux , Rats , Température du corps , Tronc cérébral , Physiologie , Potentiels évoqués auditifs du tronc cérébral , Physiologie , Fièvre , Rat Sprague-Dawley , Temps de réaction , Physiologie
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