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2006年大陆的2篇circulation [复制链接]

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离线merck
 
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只看楼主 倒序阅读 使用道具 0楼 发表于: 2006-10-15
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离线clhoucy
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只看该作者 1楼 发表于: 2006-10-15
唉,什么也不说了
离线guodon
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只看该作者 2楼 发表于: 2006-10-15
引用第0楼merck2006-10-15 22:00发表的“2006年大陆的2篇circulation”: 军科院王常勇http://circ.ahajournals.org/cgi/content/abstract/113/18/2229阜外惠汝太http://circ.ahajournals.org/cgi/content/abstract/113/12/1615

惠教授毕业于山医   呵呵

看我们的院士了
离线clhoucy
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只看该作者 3楼 发表于: 2006-10-15
实话实说,最近我们估计很难在circulation发文
不过还是需要继续努立了
相信努力会换来大文章的
这个需要不断的积累
离线小鹏8号

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只看该作者 4楼 发表于: 2006-10-15
希望山大的文章发在上面
越多越好
离线缘续来生
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只看该作者 5楼 发表于: 2006-10-16
期待中
离线南医
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只看该作者 6楼 发表于: 2006-10-16
山医会有复兴的一天的!
离线merck
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只看该作者 7楼 发表于: 2006-10-16
其实心血管专业里面JACC更接近临床,今年大陆有2篇。
1:上海泽生科技周明东
J Am Coll Cardiol. 2006 Oct 3;48(7):1438-47. Epub 2006 Sep 14.

Comment in:
  J Am Coll Cardiol. 2006 Oct 3;48(7):1448-50.

Neuregulin-1/erbB-activation improves cardiac function and survival in models of
ischemic, dilated, and viral cardiomyopathy.

Liu X, Gu X, Li Z, Li X, Li H, Chang J, Chen P, Jin J, Xi B, Chen D, Lai D,
Graham RM, Zhou M.

Zensun Sci & Tech Ltd., Shanghai, China.

OBJECTIVES: We evaluated the therapeutic potential of a recombinant 61-residue
neuregulin-1 (beta2a isoform) receptor-active peptide (rhNRG-1) in multiple
animal models of heart disease. BACKGROUND: Activation of the erbB family of
receptor tyrosine kinases by rhNRG-1 could provide a treatment option for heart
failure, because neuregulin-stimulated erbB2/erbB4 heterodimerization is not
only critical for myocardium formation in early heart development but prevents
severe dysfunction of the adult heart and premature death. Disabled
erbB-signaling is also implicated in the transition from compensatory
hypertrophy to failure, whereas erbB receptor-activation promotes myocardial
cell growth and survival and protects against anthracycline-induced
cardiomyopathy. METHODS: rhNRG-1 was administered IV to animal models of
ischemic, dilated, and viral cardiomyopathy, and cardiac function and survival
were evaluated. RESULTS: Short-term intravenous administration of rhNRG-1 to
normal dogs and rats did not alter hemodynamics or cardiac contractility. In
contrast, rhNRG-1 improved cardiac performance, attenuated pathological changes,
and prolonged survival in rodent models of ischemic, dilated, and viral
cardiomyopathy, with the survival benefits in the ischemic model being additive
to those of angiotensin-converting enzyme inhibitor therapy. In addition,
despite continued pacing, rhNRG-1 produced global improvements in cardiac
function in a canine model of pacing-induced heart failure. CONCLUSIONS: These
beneficial effects make rhNRG-1 promising as a broad-spectrum therapeutic for
the treatment of heart failure due to a variety of common cardiac diseases.

PMID: 17010808 [PubMed - indexed for MEDLINE]

2: 解放军总医院老年医学研究所何耀
J Am Coll Cardiol. 2006 Apr 18;47(8):1588-94. Epub 2006 Mar 29.

Prevalence of the metabolic syndrome and its relation to cardiovascular disease
in an elderly Chinese population.

He Y, Jiang B, Wang J, Feng K, Chang Q, Fan L, Li X, Hu FB.

Institute of Geriatrics, Chinese PLA General Hospital, Beijing, China.
yhe301@x263.net

OBJECTIVES: This study sought to assess the prevalence of the metabolic syndrome
(MetS) and its association with cardiovascular disease (CVD) in elderly Chinese
people. BACKGROUND: The information available about the prevalence of MetS based
on the National Cholesterol Education Program (NCEP) and the International
Diabetes Federation (IDF) in China is limited. METHODS: We conducted a
population-based cross-sectional study in an urban Beijing sample of 2,334
participants age 60 to 95 years (943 men, 1,391 women). The CVD included
diagnosed coronary heart disease (CHD), stroke, and peripheral arterial disease
(PAD). RESULTS: The prevalence of MetS by the NCEP criteria was 30.5% (17.6% in
men, 39.2% in women). Use of the new IDF definition significantly increased the
prevalence to 46.3% (34.8% in men, 54.1% in women). Odds ratios (OR) for CHD,
stroke, PAD, and CVD in those with MetS using the NCEP criteria were 1.43 (95%
confidence interval [CI] 1.18 to 1.74), 1.45 (95% CI 1.14 to 1.85), 1.47 (95% CI
1.18 to 1.84), and 1.50 (95% CI 1.25 to 1.81), respectively. Corresponding ORs
using new IDF criteria were 1.69 (95% CI 1.40 to 2.02), 1.58 (95% CI 1.26 to
2.00), 1.42 (95% CI 1.14 to 1.76), and 1.73 (95% CI 1.46 to 2.07), respectively.
Those who met the IDF but not the NCEP criteria (n = 436, 18.7%) had
significantly elevated ORs for CHD (1.66, 95% CI 1.31 to 2.10) and stroke (1.53,
95% CI 1.13 to 2.06). CONCLUSIONS: The MetS is highly prevalent in elderly
people in Beijing, particularly among women. Individuals with MetS defined by
either criteria are at significantly elevated ORs for CHD, stroke, and PAD. The
IDF criteria seem to be better suited than the NCEP criteria for screening and
estimating risk of MetS in Chinese people.

PMID: 16630995 [PubMed - indexed for MEDLINE]
离线merck
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只看该作者 8楼 发表于: 2006-10-16
另外一本心血管权威期刊circulation research刊发大陆一篇。
第三军医大学大坪医院心内科曾春雨
1: Circ Res. 2006 Sep 1;99(5):494-500. Epub 2006 Aug 10.

Activation of D3 dopamine receptor decreases angiotensin II type 1 receptor
expression in rat renal proximal tubule cells.

Zeng C, Liu Y, Wang Z, He D, Huang L, Yu P, Zheng S, Jones JE, Asico LD, Hopfer
U, Eisner GM, Felder RA, Jose PA.

Department of Cardiology, Daping Hospital, Third Military Medical University,
Chongqing 400042, People's Republic of China. cyzeng1@hotmail.com

The dopaminergic and renin angiotensin systems interact to regulate blood
pressure. Disruption of the D(3) dopamine receptor gene in mice produces
renin-dependent hypertension. In rats, D(2)-like receptors reduce angiotensin II
binding sites in renal proximal tubules (RPTs). Because the major D(2)-like
receptor in RPTs is the D(3) receptor, we examined whether D(3) receptors
regulate angiotensin II type 1 (AT(1)) receptors in rat RPT cells. The effect of
D(3) receptors on AT(1) receptors was studied in vitro and in vivo. The D(3)
receptor agonist PD128907 decreased AT(1) receptor protein and mRNA in WKY RPT
cells and increased it in SHR cells. PD128907 increased D(3) receptors in WKY
cells but had no effect in SHR cells. D(3)/AT(1) receptors colocalized in RPT
cells; D(3) receptor stimulation decreased the percent amount of D(3) receptors
that coimmunoprecipitated with AT(1) receptors to a greater extent in WKY than
in SHR cells. However, D(3) receptor stimulation did not change the percent
amount of AT(1) receptors that coimmunoprecipitated with D(3) receptors in WKY
cells and markedly decreased the coimmunoprecipitation in SHR cells. The D(3)
receptor also regulated the AT(1) receptor in vivo because AT(1) receptor
expression was increased in kidneys of D(3) receptor-null mice compared with
wild type littermates. D(3) receptors may regulate AT(1) receptor function by
direct interaction with and regulation of AT(1) receptor expression. One
mechanism of hypertension may be related to increased renal expression of AT(1)
receptors due decreased D(3) receptor regulation.

PMID: 16902178 [PubMed - indexed for MEDLINE]
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