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91.
92.
We have known for some time that the epidemiology of human stroke is sexually dimorphic until late in life, well beyond the
years of reproductive senescence and menopause. Now, a new concept is emerging: the mechanisms and outcome of cerebral ischemic injury are influenced strongly by biological sex as well as the availability of sex steroids to the
brain. The principal mammalian estrogen (17 β estradiol or E2) is neuroprotective in many types of brain injury and has been
the major focus of investigation over the past several decades. However, it is becoming increasingly clear that although hormones
are a major contributor to sex-specific outcomes, they do not fully account for sex-specific responses to cerebral ischemia.
The purpose of this review is to highlight recent studies in cell culture and animal models that suggest that genetic sex
determines experimental stroke outcome and that divergent cell death pathways are activated after an ischemic insult. These
sex differences need to be identified if we are to develop efficacious neuroprotective agents for use in stroke patients. 相似文献
93.
Berriman M Hall N Sheader K Bringaud F Tiwari B Isobe T Bowman S Corton C Clark L Cross GA Hoek M Zanders T Berberof M Borst P Rudenko G 《Molecular and biochemical parasitology》2002,122(2):131-140
Trypanosoma brucei evades the immune system by switching between Variant Surface Glycoprotein (VSG) genes. The active VSG gene is transcribed in one of approximately 20 telomeric expression sites (ESs). It has been postulated that ES polymorphism plays a role in host adaptation. To gain more insight into ES architecture, we have determined the complete sequence of Bacterial Artificial Chromosomes (BACs) containing DNA from three ESs and their flanking regions. There was variation in the order and number of ES-associated genes (ESAGs). ESAGs 6 and 7, encoding transferrin receptor subunits, are the only ESAGs with functional copies in every ES that has been sequenced until now. A BAC clone containing the VO2 ES sequences comprised approximately half of a 330 kb 'intermediate' chromosome. The extensive similarity between this intermediate chromosome and the left telomere of T. brucei 927 chromosome I, suggests that this previously uncharacterised intermediate size class of chromosomes could have arisen from breakage of megabase chromosomes. Unexpected conservation of sequences, including pseudogenes, indicates that the multiple ESs could have arisen through a relatively recent amplification of a single ES. 相似文献
94.
Jason B. Mattingley Louise A. Corben John L. Bradshaw Judy A. Bradshaw Jim G. Phillips Malcolm K. Horne 《Experimental brain research. Experimentelle Hirnforschung. Expérimentation cérébrale》1998,120(2):243-256
Patients with unilateral neglect following right hemisphere damage may have difficulty in moving towards contralesional targets.
To test the hypothesis that this impairment arises from competing motor programs triggered by irrelevant ipsilesional stimuli,
we examined 16 right hemisphere patients, eight with left visual neglect and eight without, in addition to eight healthy control
subjects. In experiment 1 subjects performed sequences of movements using their right hand to targets on the contralesional
or ipsilesional side of the responding limb. The locations of successive targets in each sequence were either predictable
or unpredictable. In separate blocks of trials, targets appeared either alone or with a simultaneous distractor located at
the immediately preceding target location. Neglect patients were significantly slower to execute movements to contralesional
targets, but only for unpredictable movements and in the presence of a concurrent ipsilesional distractor. In contrast, healthy
controls and right hemisphere patients without neglect showed no directional asymmetries of movement execution. In experiment
2 subjects were required to interrupt a predictable, reciprocating sequence of leftward and rightward movements in order to
move to an occasional, unpredictable target that occurred either in the direction opposite to that expected, or in the same
direction but twice the extent. Neglect patients were significantly slower in reprogramming the direction and extent of movements
towards contralesional versus ipsilesional targets, and they also made significantly more errors when executing such movements.
Right hemisphere patients without neglect showed a similar bias in reprogramming direction (but not extent) for contralesional
targets, whereas healthy controls showed no directional asymmetry in either condition. On the basis of these findings we propose
that neglect involves a competitive bias in favour of motor programs for actions directed towards ipsilesional versus contralesional
events. We suggest that programming errors and increased latencies for contralesional movements arise because the damaged
right hemisphere can no longer effectively inhibit the release of inappropriate motor programs towards ipsilesional events.
Received: 1 October 1996 / Accepted: 21 October 1997 相似文献
95.
A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13 总被引:12,自引:5,他引:12
Francis Michael J.; Morrison Karen E.; Campbell Louise; Grewal Prabhjit K.; Christodoulou Zoe; Daniels Rachael J.; Monaco Anthony P.; Frischauf Anne-Marie; McPherson John; Wasmuth John; Davies Kay E. 《Human molecular genetics》1993,2(8):1161-1167
We have constructed a contig of non-chimaeric yeast artificialchromosomes (YACs) across the candidate region for childhoodautosomal recessive spinal muscular atrophy (SMA) In 5q13. Anovel microsatellite reduces the candidate region to approximately400kb of DNA distal to D5S435. The candidate region containsblocks of chromosome 5 specific repeats which have copies on5p as well as elsewhere on 5q. Restriction mapping of the YACsreveals at least one CpG island In the SMA gene region. TheYAC maps indicate that the contig contains minimal rearrangementsor deletions. The data show the value of screening several YAClibraries simultaneously in order to construct a set of overlappingsequences suitable for candidate gene searches and direct genomicsequencing. 相似文献
96.
97.
This cross‐sectional study identified variables associated with protease inhibitor (PI) non‐adherence in 179 patients taking anti‐retroviral therapy. Univariate analyses identified 11 variables associated with PI non‐adherence. Multiple logistic regression modelling identified three predictors of PI non‐adherence: low adherence self‐efficacy and seriousness of non‐adherence and HIV (p < .001), perceived absence of HIV associated illness (p < .01), and use of more than one type of recreational drug (p = .001). The model correctly classified 83.9% of the sample, offers psychologists insight into psychological barriers to treatment adherence to guide interventions for improving adherence, and supports a modified version of the reformulated health belief model. 相似文献
98.
T. A. Reader F.R.S.Q. R. Brière Louise Grondin 《Journal of neural transmission (Vienna, Austria : 1996)》1987,68(1-2):79-95
Summary The tritiated adrenergic antagonists prazosin ([3H]PRZ) and idazoxan ([3H]IDA, or RX-781094) bind specifically and with high affinity in membrane preparations from cerebral cortex to alpha-1- and alpha-2-adrenoceptors respectively. Saturation experiments, performed to determine the density of receptors (Bmax; maximum binding capacity) and the dissociation constant (Kd 25 °C), were analyzed by the methods of Eadie and Hofstee, iterative modelling, and the procedure of Hill. The pharmacologic properties and specificity of the labelling was verified by displacement experiments using alpha-adrenergic antagonists and agonists. The antagonist drugs showed the following order of potency to displace [3H]prazosin: prazosin phentolamine corynanthine > pyrextramine yohimbine piperoxan > benextramine > idazoxan; for the agonists: clonidine (–)-noradrenaline (–)-adrenaline phenylephrine, while other drugs, such as (–)-propranolol, dopamine, (–)-isoproterenol and serotonin only competed with the alpha-1-ligand at concentrations above 20 M. The alpha2-sites labelled by [3H]idazoxan were characterized by the antagonist displacement sequence idazoxan phentolamine > yohimbine = > piperoxan pyrextramine benextramine prazosin corynanthine. The agonists order of potency to compete with [3H]idazoxan was clonidine phenylephrine = > (–)-adrenaline > (–)-noradrenaline, and for other related drugs it was (–)-propranolol dopamine serotonin > (–)-isoproterenol. These competition experiments clearly showed two pharmacologically distinct sites, but question the relative specificity of some of the adrenergic drugs.Abreviations [3H]PRZ
[3H]prazosin
- [3H]IDA
[3H]idazoxan
- Bmax
maximum binding capacity
- Kd
dissociation constant
- IC 50
inhibitory concentration that reduces binding by 50%
- Ki
inhibition-dissociation constant
- nH
Hill coefficient
- CMC
coefficient of multiple correlation
- fmol/mg p
fentomoles per mg of protein
- nM
nanomolar
Recipient of a F.R.S.Q. Studentship. 相似文献
99.
Power Thomas G. Garcia Karina Silva Martinez AnaMaria Diaz Parker Louise A. Hidalgo-Mendez Jackelyn Ramos Guadalupe 《Prevention science》2022,23(6):1018-1028
Prevention Science - “Madres Apoyando el Desarrollo Emocional de Sus Hijos” (“Mothers Supporting the Emotional Development of Their Children”) is a parenting... 相似文献
100.
Ryan Gage Martin Girling-Butcher Ester Joe Moira Smith Cliona Ni Mhurchu Christina McKerchar Viliami Puloka Rachael McLean Louise Signal 《Nutrients》2021,13(1)
Snacking is a common eating behaviour, but there is little objective data about children’s snacking. We aimed to determine the frequency and context of children’s snacking (n = 158; mean age = 12.6 years) by ethnicity, gender, socioeconomic deprivation and body mass index (BMI) children. Participants wore wearable cameras that passively captured images of their surroundings every seven seconds. Images (n = 739,162) were coded for snacking episodes, defined as eating occasions in between main meals. Contextual factors analysed included: snacking location, food source, timing, social contact and screen use. Rates of total, discretionary (not recommended for consumption) and healthful (recommended for consumption) snacking were calculated using negative binomial regression. On average, children consumed 8.2 (95%CI 7.4, 9.1) snacks per day, of which 5.2 (95%CI 4.6, 5.9) were discretionary foods/beverages. Children consumed more discretionary snacks than healthful snacks in each setting and at all times, including 15.0× more discretionary snacks in public spaces and 2.4× more discretionary snacks in schools. Most snacks (68.9%) were sourced from home. Girls consumed more total, discretionary and healthful snacks than boys, and Māori and Pacific consumed fewer healthful snacks than New Zealand (NZ) Europeans. Results show that children snack frequently, and that most snacking involves discretionary food items. Our findings suggest targeting home buying behaviour and environmental changes to support healthy snacking choices. 相似文献