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本文引用的文献

1
Spatial frequency threshold and contrast sensitivity of an optomotor behavior are impaired in the Ins2Akita mouse model of diabetes.糖尿病 Ins2Akita 小鼠模型的光感受器运动行为的空间频率阈值和对比敏感度受损。
Behav Brain Res. 2012 Jan 15;226(2):601-5. doi: 10.1016/j.bbr.2011.09.030. Epub 2011 Sep 28.
2
Layer-specific functional and anatomical MRI of the retina with passband balanced SSFP.带通平衡稳态自由进动(SSFP)视网膜的层特异性功能和解剖 MRI
Magn Reson Med. 2011 Nov;66(5):1416-21. doi: 10.1002/mrm.22935. Epub 2011 May 20.
3
MRI of retinal and choroidal blood flow with laminar resolution.层分辨力视网膜和脉络膜血流的 MRI 成像。
NMR Biomed. 2011 Feb;24(2):216-23. doi: 10.1002/nbm.1576. Epub 2010 Sep 6.
4
Retinal blood flow in type 1 diabetic patients with no or mild diabetic retinopathy during euglycemic clamp.1 型糖尿病患者无或轻度糖尿病视网膜病变在血糖钳夹期间的视网膜血流。
Diabetes Care. 2010 Sep;33(9):2038-42. doi: 10.2337/dc10-0502. Epub 2010 Jun 28.
5
Reduced retinal blood flow velocity in diabetic retinopathy.糖尿病性视网膜病变患者视网膜血流速度降低。
Retina. 2010 May;30(5):765-73. doi: 10.1097/IAE.0b013e3181c596c6.
6
Activation of the Wnt pathway plays a pathogenic role in diabetic retinopathy in humans and animal models.Wnt 通路的激活在人类和动物模型的糖尿病性视网膜病变中起着致病作用。
Am J Pathol. 2009 Dec;175(6):2676-85. doi: 10.2353/ajpath.2009.080945. Epub 2009 Nov 5.
7
Type 1 diabetic cardiomyopathy in the Akita (Ins2WT/C96Y) mouse model is characterized by lipotoxicity and diastolic dysfunction with preserved systolic function.1 型糖尿病心肌病在 Akita(Ins2WT/C96Y)小鼠模型中表现为脂毒性和舒张功能障碍,收缩功能正常。
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8
Role of SREBP-1 in the development of parasympathetic dysfunction in the hearts of type 1 diabetic Akita mice.固醇调节元件结合蛋白-1(SREBP-1)在1型糖尿病秋田小鼠心脏副交感神经功能障碍发生中的作用
Circ Res. 2009 Jul 31;105(3):287-94. doi: 10.1161/CIRCRESAHA.109.193995. Epub 2009 May 7.
9
Erythrocyte flow in choriocapillaris of normal and diabetic rats.正常和糖尿病大鼠脉络膜毛细血管中的红细胞流动
Microvasc Res. 2009 May;77(3):247-55. doi: 10.1016/j.mvr.2009.02.003. Epub 2009 Mar 6.
10
Diabetic myopathy differs between Ins2Akita+/- and streptozotocin-induced Type 1 diabetic models.糖尿病性肌病在Ins2Akita+/-小鼠模型和链脲佐菌素诱导的1型糖尿病模型中存在差异。
J Appl Physiol (1985). 2009 May;106(5):1650-9. doi: 10.1152/japplphysiol.91565.2008. Epub 2009 Feb 26.

糖尿病模型小鼠中眼血流减少可作为糖尿病性视网膜病变的早期指标。

Reduced ocular blood flow as an early indicator of diabetic retinopathy in a mouse model of diabetes.

机构信息

Research Imaging Institute, University of Texas Health Science Center, San Antonio, Texas 78229, USA.

出版信息

Invest Ophthalmol Vis Sci. 2012 Sep 21;53(10):6488-94. doi: 10.1167/iovs.12-9758.

DOI:10.1167/iovs.12-9758
PMID:22915034
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4045095/
Abstract

PURPOSE

To investigate ocular blood flow and visual function in the Ins2(Akita) diabetic retinopathy mouse model at early and late time points after onset of hyperglycemia.

METHODS

Mice heterozygous for the Ins2(Akita) mutation, which become hyperglycemic at approximately 4 weeks old, were studied at 2.5 and 7.5 months of age, with age-matched wild-type littermates used as controls. Retinal and choroidal blood flows were noninvasively imaged at 42 × 42 × 400 μm using magnetic resonance imaging. Visual function was measured using optokinetic tracking to determine spatial frequency and contrast thresholds from the same mice.

RESULTS

At 2.5 months, choroidal blood flow was significantly reduced (P < 0.01) by 20% in Ins2(Akita) mice (n = 13) compared with age-matched controls (n = 16), whereas retinal blood flow and visual function were not significantly affected (P > 0.05). At 7.5 months, both choroidal and retinal blood flow were significantly reduced (P < 0.05) by 27% and 28%, respectively, in Ins2(Akita) mice (n = 11) compared with age-matched controls (n = 15). Visual functions were also significantly worse (P < 0.05) in Ins2(Akita) mice at 7.5 months, as indicated by a 19% decreased spatial frequency threshold and 135% increased contrast threshold compared with age-matched controls. The magnitudes of the blood flow and vision deficits, however, were not correlated.

CONCLUSIONS

Although both choroidal and retinal blood flow and vision were altered after prolonged diabetes in the Ins2(Akita) mouse, choroidal blood flow was reduced even in young diabetic animals, suggesting ocular blood flow deficit could be an early pathological change in diabetic retinopathy.

摘要

目的

在 Ins2(Akita)糖尿病视网膜病变小鼠模型中,研究高血糖发生后早期和晚期眼血流和视觉功能。

方法

Ins2(Akita)突变杂合子小鼠在大约 4 周龄时发生高血糖,在 2.5 和 7.5 个月大时进行研究,并用年龄匹配的野生型同窝仔鼠作为对照。使用磁共振成像在 42×42×400μm 范围内非侵入性地对视网膜和脉络膜血流进行成像。使用视动跟踪测量视觉功能,从同一批小鼠中确定空间频率和对比度阈值。

结果

在 2.5 个月时,与年龄匹配的对照组(n = 16)相比,Ins2(Akita)小鼠(n = 13)的脉络膜血流显著减少(P < 0.01),减少了 20%,而视网膜血流和视觉功能没有受到显著影响(P > 0.05)。在 7.5 个月时,Ins2(Akita)小鼠(n = 11)的脉络膜和视网膜血流分别显著减少(P < 0.05)27%和 28%,与年龄匹配的对照组(n = 15)相比。Ins2(Akita)小鼠的视觉功能也明显更差(P < 0.05),与年龄匹配的对照组相比,空间频率阈值降低了 19%,对比度阈值增加了 135%。然而,血流和视力缺陷的严重程度没有相关性。

结论

尽管在 Ins2(Akita)小鼠中,延长糖尿病后,脉络膜和视网膜血流以及视力都发生了改变,但在年轻的糖尿病动物中,脉络膜血流已经减少,这表明眼部血流不足可能是糖尿病视网膜病变的早期病理变化。