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排序方式: 共有117条查询结果,搜索用时 9 毫秒
1.
Attard Ritienne Dingli Philip Doggen Carine J. M. Cassar Karen Farrugia Rosienne Bezzina Wettinger Stephanie 《Zeitschrift fur Gesundheitswissenschaften》2021,29(3):611-624
Journal of Public Health - To determine the risk of myocardial infarction (MI) associated with pattern, frequency, and intensity of alcohol consumption, type of alcoholic beverage, and the combined... 相似文献
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Duane's retraction syndrome is sometimes associated with developmental ocular and extraocular abnormalities. This disorder may also be present in association with specific malformative syndromes. The authors report the clinical features of a seven-year-old female affected by Duane's retraction syndrome (D.R.S.), rectoperineal fistula, imperforate anus and other congenital malformations. From two extensive reviews of 106 reports published before 1982 and from a search (using Medline 1981-1994) for reports of congenital malformations associated with this syndrome, no cases of sporadic D.R.S. associated with the perineal malformations mentioned were found, even though imperforate anus is considered the commoner of hindgut malformation. 相似文献
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Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 下载免费PDF全文
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Effects of quinolinic acid-induced lesions of the nucleus accumbens core on inter-temporal choice: a quantitative analysis 总被引:1,自引:1,他引:0
Bezzina G Cheung TH Asgari K Hampson CL Body S Bradshaw CM Szabadi E Deakin JF Anderson IM 《Psychopharmacology》2007,195(1):71-84
Rationale There is evidence that lesions of the nucleus accumbens core (AcbC) promote preference for smaller earlier reinforcers over
larger delayed reinforcers in inter-temporal choice paradigms. It is not known whether this reflects an effect of the lesion
on the rate of delay discounting, on sensitivity to reinforcer magnitude, or both.
Aim We examined the effect of AcbC lesions on inter-temporal choice using a quantitative method that allows effects on delay discounting
to be distinguished from effects on sensitivity to reinforcer size.
Materials and methods Sixteen rats received bilateral quinolinic acid-induced lesions of the AcbC; 14 received sham lesions. They were trained under
a discrete-trials progressive delay schedule to press two levers (A and B) for a sucrose solution. Responses on A delivered
50 μl of the solution after a delay d
A; responses on B delivered 100 μl after d
B. d
B increased across blocks of trials, while d
A was manipulated across phases of the experiment. Indifference delay d
B(50) (value of d
B corresponding to 50% choice of B) was estimated in each phase, and linear indifference functions (d
B(50) vs d
A) derived.
Results
d
B(50) increased linearly with d
A (r
2 > 0.95 in each group). The intercept of the indifference function was lower in the lesioned than the sham-lesioned group;
slope did not differ between groups. The lesioned rats had extensive neuronal loss in the AcbC.
Conclusions The results confirm that lesions of the AcbC promote preference for smaller, earlier reinforcers and suggest that this reflects
an effect of the lesion on the rate of delay discounting. 相似文献
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Characterization of a novel SCN5A mutation associated with Brugada syndrome reveals involvement of DIIIS4-S5 linker in slow inactivation 总被引:1,自引:0,他引:1
Casini S Tan HL Bhuiyan ZA Bezzina CR Barnett P Cerbai E Mugelli A Wilde AA Veldkamp MW 《Cardiovascular research》2007,76(3):418-429
OBJECTIVE: Mutations in SCN5A, the gene encoding the alpha-subunit of the cardiac sodium channel (Na(v)1.5), have been associated with various inherited arrhythmia syndromes, including Brugada syndrome (BrS). Here, we report the functional consequences of a novel missense SCN5A mutation, G1319V, identified in a BrS patient. The G1319V mutation is located in the loop connecting transmembrane segments 4 and 5 in domain III (DIIIS4-S5), a region so far considered to be exclusively involved in fast inactivation. METHODS: Whole-cell mutant (G1319V) and wild-type (WT) sodium currents (I(Na)) were studied in the Human Embryonic Kidney cell line (HEK-293) transfected with Na(v)1.5 alpha-subunit cDNA (WT or mutant) together with hbeta(1)-subunit cDNA, using the patch-clamp technique. RESULTS: Maximal peak I(Na) and persistent sodium current were similar in WT and channel G1319V channels. The G1319V mutation shifted the potential of half-maximal (V(1/2)) activation towards more positive potentials (+3.7 mV), thereby increasing the degree of depolarization required for activation. The V(1/2) of inactivation of G1319V channels was shifted by -6.0 mV compared to WT, resulting in a reduced channel availability. The change in the steady-state inactivation was completely due to a negative shift (-6.8 mV) of the voltage-dependence of slow inactivation, while the voltage-dependence of fast inactivation was unaffected. The fast component of recovery from inactivation of G1319V channels was slowed down. Finally, the G1319V mutation caused a two-fold increase in the propensity of the channels to enter the slow inactivated state. Reduction in I(Na) peak amplitude on repetitive depolarizations at short interpulse intervals (40 ms) was significantly more pronounced in G1319V compared to WT. Accordingly, carriers of the G1319V mutation showed marked QRS widening upon increases in heart rate during exercise testing, pointing to enhancement of slow inactivation. CONCLUSIONS: We identified the DIIIS4-S5 linker as a new region involved in slow inactivation of Na(v)1.5. The biophysical alterations of the G1319V mutation all contribute to a reduction in I(Na), in line with the proposed mechanism underlying BrS. 相似文献
10.
Veldkamp MW Wilders R Baartscheer A Zegers JG Bezzina CR Wilde AA 《Circulation research》2003,92(9):976-983
One variant of the long-QT syndrome (LQT3) is caused by mutations in the human cardiac sodium channel gene. In addition to the characteristic QT prolongation, LQT3 carriers regularly present with bradycardia and sinus pauses. Therefore, we studied the effect of the 1795insD Na+ channel mutation on sinoatrial (SA) pacemaking. The 1795insD channel was previously characterized by the presence of a persistent inward current (Ipst) at -20 mV and a negative shift in voltage dependence of inactivation. In the present study, we first additionally characterized Ipst over the complete voltage range of the SA node action potential (AP) by measuring whole-cell Na+ currents (INa) in HEK-293 cells expressing either wild-type or 1795insD channels. Ipst for 1795insD channels varied between 0.8+/-0.2% and 1.9+/-0.8% of peak INa. Activity of 1795insD channels during SA node pacemaking was confirmed by AP clamp experiments. Next, Ipst and the negative shift were implemented into SA node AP models. The -10-mV shift decreased sinus rate by decreasing diastolic depolarization rate, whereas Ipst decreased sinus rate by AP prolongation, despite a concomitant increase in diastolic depolarization rate. In combination, moderate Ipst (1% to 2%) and the shift reduced sinus rate by approximately 10%. An additional increase in Ipst could result in plateau oscillations and failure to repolarize completely. Thus, Na+ channel mutations displaying an Ipst or a negative shift in inactivation may account for the bradycardia seen in LQT3 patients, whereas SA node pauses or arrest may result from failure of SA node cells to repolarize under conditions of extra net inward current. 相似文献