Urine-based Detection of Congenital Portosystemic Shunt in C57BL/6 Mice.
Urine-based Detection of Congenital Portosystemic Shunt in C57BL/6 Mice.
复制标题
C57BL/6小鼠先天性门体分流的尿液检测
DOI:
10.1093/function/zqad040
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发表时间:
2023
期刊:
影响因子:
6.2
通讯作者:
Vijay-Kumar, Matam
中科院分区:
文献类型:
--
作者:
Yeoh, Beng San;Golonka, Rachel M.;Saha, Piu;Kandalgaonkar, Mrunmayee R.;Tian, Yuan;Osman, Islam;Patterson, Andrew D.;Gewirtz, Andrew T.;Joe, Bina;Vijay-Kumar, Matam
Sporadic occurrence of congenital portosystemic shunt (PSS) at a rate of ∼1 out of 10 among C57BL/6 J mice, which are widely used in biomedical research, results in aberrancies in serologic, metabolic, and physiologic parameters. Therefore, mice with PSS should be identified as outliers in research. Accordingly, we sought methods to, reliably and efficiently, identify PSS mice. Serum total bile acids ≥ 40 µm is a bona fide biomarker of PSS in mice but utility of this biomarker is limited by its cost and invasiveness, particularly if large numbers of mice are to be screened. This led us to investigate if assay of urine might serve as a simple, inexpensive, noninvasive means of PSS diagnosis. Metabolome profiling uncovered that Krebs cycle intermediates, that is, citrate, α-ketoglutarate, and fumarate, were strikingly and distinctly elevated in the urine of PSS mice. We leveraged the iron-chelating and pH-lowering properties of such metabolites as the basis for 3 urine-based PSS screening tests: urinary iron-chelation assay, pH strip test, and phenol red assay. Our findings demonstrate the feasibility of using these colorimetric assays, whereby their readout can be assessed by direct observation, to diagnose PSS in an inexpensive, rapid, and noninvasive manner. Application of our urinary PSS screening protocols can aid biomedical research by enabling stratification of PSS mice, which, at present, likely confound numerous ongoing studies. Urinalysis to detect portosystemic shunt in mice.
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影响因子:
3.7
作者:
Ronda OAHO;van de Heijning BJM;de Bruin A;Thomas RE;Martini I;Koehorst M;Gerding A;Koster MH;Bloks VW;Jurdzinski A;Mulder NL;Havinga R;van der Beek EM;Reijngoud DJ;Kuipers F;Verkade HJ
通讯作者:
Verkade HJ
影响因子:
64.5
作者:
Singh V;Yeoh BS;Chassaing B;Xiao X;Saha P;Aguilera Olvera R;Lapek JD Jr;Zhang L;Wang WB;Hao S;Flythe MD;Gonzalez DJ;Cani PD;Conejo-Garcia JR;Xiong N;Kennett MJ;Joe B;Patterson AD;Gewirtz AT;Vijay-Kumar M
通讯作者:
Vijay-Kumar M
影响因子:
13.5
作者:
Glantz, A;Marschall, HW;Mattsson, LÅ
通讯作者:
Mattsson, LÅ
DOI:
10.1073/pnas.190256997
发表时间:
2000-09-12
影响因子:
11.1
作者:
Lahvis, GP;Lindell, SL;Bradfield, CA
通讯作者:
Bradfield, CA
DOI:
10.1152/ajpendo.00332.2001
发表时间:
2002-04-01
影响因子:
5.1
作者:
Burcelin, M;Crivelli, V;Thorens, B
通讯作者:
Thorens, B