Endogenous metabolite; glycine-conjugated secondary bile acid

石胆酸（LCA）是一种与胆汁淤积等不良反应相关的胆汁酸，在体内主要以Glycolithocholic acid（GLCA）和tauro-LCA（TLCA）的结合物存在。三苯氧胺与胆汁淤积的发展有关，它抑制磺基转移酶2A1（SULT2A1）催化的脱氢表雄酮（DHEA）磺化。本研究旨在表征LCA、GLCA和TLCA的磺化作用，并研究选择性雌激素受体调节剂（SERM）类的三苯乙烯（氯米芬、三苯氧胺、托瑞米芬、奥赛美芬、屈洛昔芬）、苯并噻吩（雷洛昔芬、阿唑昔芬）、四氢萘（拉索昔芬、萘呋辛）、吲哚（巴多昔芬）和苯并吡喃（acolbifene）是否抑制LCA、GLPA和TLCA磺化。人重组SULT2A1，但不是SULT2B1b或SULT1E1，催化LCA、GLCA和TLCA磺化，而这些酶中的每一种都催化DHEA磺化。LCA、GLCA和TLCA磺化由人肝细胞溶质催化，SULT2A1遵循底物抑制模型，具有相当的表观Km值（≤1µm）。每种SERM都以不同的效力和酶抑制模式抑制LCA、GLCA和TLCA磺化。通过对托瑞米芬、巴多昔芬和拉索菲芬进行结构修饰，LCA磺化的效力和抑制程度减弱或增加。在HepG2人肝细胞癌细胞中也观察到雷洛昔芬、巴多昔芬和阿可联苯对LCA磺化的抑制作用。总体而言，在所研究的SERM中，巴多昔芬和雷洛昔芬是LCA、GLCA和TLCA磺化最有效的抑制剂。这些发现为特定SERM的结构特征提供了见解，这些特征有助于抑制SULT2A1催化的LCA磺化。SERM对LCA、GLCA和TLCA解毒的抑制可能为SERM相关的不良反应提供生化基础[3]。

在杂合FH IIa型患者中，我们观察到与对照组的相应值相比，甘鹅脱氧胆酸、甘熊脱氧胆酸和Glycolithocholic acid的摩尔百分比显著降低，牛磺脱氧胆酸显著增加。在普罗布考治疗16周后，对6名患者的胆汁分析进行了复查。普罗布考显著降低了血清胆固醇水平。然而，治疗没有改变胆汁脂质组成和单个胆汁酸比例。结果表明，大多数杂合性FH患者胆汁过饱和，易形成胆固醇结石。此外，普罗布考降低血清胆固醇的机制似乎与胆汁脂质代谢的任何变化无关。[1]

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结果：本研究纳入了32名UC患者和23名HC患者。研究发现，与HC相比，UC患者的肠道微生物群多样性降低。UC患者的厚壁菌门、梭菌IV、丁球菌、梭菌XlVa、粪杆菌和Roseburia显著降低（分别为P=0.75E-05、P=0.28E-07、P=0.0002、P=0.003、P=0.0003和P=0.0004）。UC组中变形杆菌、大肠杆菌、肠球菌、克雷伯氏菌和链球菌显著富集（分别为P=2.99E-09、P=3.63E-05、P=8.59E-05、P=0.003和P=0.016）。UC患者粪便中的继发性BAs，如石胆酸、脱氧胆酸、糖脱氧胆酸、Glycolithocholic acid和牛磺胆酸的浓度显著低于HCs（分别为P=8.1E-08、P=1.2E-07、P=3.5E-04、P=1.9E-03和P=1.8E-02），并与丁球菌、玫瑰孢菌、梭菌IV、粪杆菌和梭菌XlVb呈正相关（P<0.01）。UC患者的原发性BA，如牛磺胆酸、胆酸、牛磺脱氧胆酸和甘鹅脱氧胆酸的浓度显著高于HC患者（分别为P=5.3E-03、P=4E-02、P=0.042和P=0.045），并且与肠球菌、克雷伯氏菌、链球菌、乳杆菌和促炎细胞因子呈正相关（P<0.01）。UC患者TGR5的表达显著升高（0.019±0.013 vs 0.006±0.003，P=0.0003）。UC患者结肠黏膜标本中VDR表达显著降低（0.011±0.007 vs 0.016±0.004，P=0.033）。 结论：粪便BA谱与肠道微生物群和血清炎性细胞因子密切相关。肠道微生物群失调和粪便BAs结构改变可能通过BA受体TGR5和VDR参与调节炎症反应[2]。

LCA、GLCA/Glycolithocholic acid、TLCA和DHEA磺化试验的优化[3]
之前已经优化了人肝细胞质中的LCA磺化试验（Bansal和Lau，2016a）。LCA和GLCA/Glycolithocholic acid磺化在100µg细胞质蛋白时线性增加，而TLCA磺化在80µg细胞质蛋白质时线性增加（补充图S1，A-C）。重组SULT2A1催化的LCA、Glycolithocholic acid/GLCA和TLCA磺化在5µg酶下呈线性（补充图S1，D-F）。人肝细胞溶质催化LCA磺化反应在45分钟内呈线性，而GLCA在45分钟后呈线性。。。

Background: Gut microbiota and its metabolites may be involved in the pathogenesis of inflammatory bowel disease. Several clinical studies have recently shown that patients with ulcerative colitis (UC) have altered profiles of fecal bile acids (BAs). It was observed that BA receptors Takeda G-protein-coupled receptor 5 (TGR5) and vitamin D receptor (VDR) participate in intestinal inflammatory responses by regulating NF-ĸB signaling. We hypothesized that altered profiles of fecal BAs might be correlated with gut microbiota and inflammatory responses in patients with UC. Aim: To investigate the changes in fecal BAs and analyze the relationship of BAs with gut microbiota and inflammation in patients with UC. Methods: The present study used 16S rDNA sequencing technology to detect the differences in the intestinal flora between UC patients and healthy controls (HCs). Fecal BAs were measured by targeted metabolomics approaches. Mucosal TGR5 and VDR expression was analyzed using immunohistochemistry, and serum inflammatory cytokine levels were detected by ELISA.[2]

[1]. Biliary lipid composition in heterozygous familial hypercholesterolemia and influence of treatment with probucol. Dig Dis Sci. 1994 Jul;39(7):1586-91.

[2]. Altered profiles of fecal bile acids correlate with gut microbiota and inflammatory responses in patients with ulcerative colitis. World J Gastroenterol. 2021 Jun 28;27(24):3609-3629.

[3]. Inhibition of Human Sulfotransferase 2A1-Catalyzed Sulfonation of Lithocholic Acid, Glycolithocholic Acid, and Taurolithocholic Acid by Selective Estrogen Receptor Modulators and Various Analogs and Metabolites. J Pharmacol Exp Ther. 2019 Jun;369(3):389-405.

[4]. Potent suppression of hydrophobic bile acids by aldafermin, an FGF19 analogue, across metabolic and cholestatic liver diseases. JHEP Rep. 2021 Feb 19;3(3):100255.

Glycolithocholic acid is the glycine conjugate of lithocholic acid. It is a bile acid glycine conjugate and a N-acylglycine. It is functionally related to a lithocholic acid. It is a conjugate acid of a glycolithocholate.
Glycolithocholic acid has been reported in Homo sapiens and Bos taurus with data available.
See also: Glycolithocholate (annotation moved to).

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Background & aims: Higher serum bile acid levels are associated with an increased risk of cirrhosis and liver-related morbidity and mortality. Herein, we report secondary analyses of aldafermin, an engineered analogue of the gut hormone fibroblast growth factor 19, on the circulating bile acid profile in prospective, phase II studies in patients with metabolic or cholestatic liver disease. Methods: One hundred and seventy-six patients with biopsy-confirmed non-alcoholic steatohepatitis (NASH) and fibrosis and elevated liver fat content (≥8% by magnetic resonance imaging-proton density fat fraction) received 0.3 mg (n = 23), 1 mg (n = 49), 3 mg (n = 49), 6 mg (n = 28) aldafermin or placebo (n = 27) for 12 weeks. Sixty-two patients with primary sclerosing cholangitis (PSC) and elevated alkaline phosphatase (>1.5× upper limit of normal) received 1 mg (n = 21), 3 mg (n = 21) aldafermin or placebo (n = 20) for 12 weeks. Serum samples were collected on day 1 and week 12 for determination of bile acid profile and neoepitope-specific N-terminal pro-peptide of type III collagen (Pro-C3), a direct measure of fibrogenesis. Results: Treatment with aldafermin resulted in significant dose-dependent reductions in serum bile acids. In particular, bile acids with higher hydrophobicity indices, such as deoxycholic acid, lithocholic acid, glycodeoxycholic acid, glycochenodeoxycholic acid, and glycocholic acid, were markedly lowered by aldafermin in both NASH and PSC populations. Moreover, aldafermin predominantly suppressed the glycine-conjugated bile acids, rather than the taurine-conjugated bile acids. Changes in levels of bile acids correlated with changes in the novel fibrogenesis marker Pro-C3, which detects a neo-epitope of the type III collagen during its formation, in the pooled NASH and PSC populations. Conclusions: Aldafermin markedly reduced major hydrophobic bile acids that have greater detergent activity and cytotoxicity. Our data provide evidence that bile acids may contribute to sustaining a pro-fibrogenic microenvironment in the liver across metabolic and cholestatic liver diseases. Lay summary: Aldafermin is an analogue of a gut hormone, which is in development as a treatment for patients with chronic liver disease. Herein, we show that aldafermin can potently and robustly suppress the toxic, hydrophobic bile acids irrespective of disease aetiology. The therapeutic strategy utilising aldafermin may be broadly applicable to other chronic gastrointestinal and liver disorders. Clinical trials registration: The study is registered at Clinicaltrials.govNCT02443116 and NCT02704364.[4]

C26H42NO4-.NA+

455.60578

455.301

24404-83-9

Glycolithocholic acid;474-74-8;Glycolithocholic acid-d4;2044276-16-4

23688920

White to off-white solid powder

619.7ºC at 760 mmHg

328.6ºC

3.679

89.46

2

4

6

32

701

6

C[C@H](CCC(=NCC(=O)O)[O-])[C@H]1CCC2C3CCC4C[C@@H](CC[C@]4(C)C3CC[C@]12C)O.[Na+]

LQKBJAKZKFBLIB-NYTIRPLLSA-M

InChI=1S/C26H43NO4.Na/c1-16(4-9-23(29)27-15-24(30)31)20-7-8-21-19-6-5-17-14-18(28)10-12-25(17,2)22(19)11-13-26(20,21)3;/h16-22,28H,4-15H2,1-3H3,(H,27,29)(H,30,31);/q;+1/p-1/t16-,17-,18-,19?,20-,21?,22?,25+,26-;/m1./s1

sodium;2-[[(4R)-4-[(3R,5R,10S,13R,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]acetate

Glycolithocholic acid sodium salt; GLYCOLITHOCHOLIC ACID, SODIUM SALT; 24404-83-9; Glycolithocholic acid (sodium); Sodium ((4R)-4-((3R,10S,13R,17R)-3-hydroxy-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoyl)glycinate; Sodium Glycolithocholate; N-(3alpha-Hydroxy-5beta-cholan-24-oyl)glycine Sodium Salt; N-[(3alpha,5beta)-3-Hydroxy-24-oxocholan-24-yl]glycine Sodium Salt;; Lithocholylglycine (sodium); Glycolithocholic acid,sodium salt;

2934.99.9001

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)

DMSO : ~25 mg/mL (~54.87 mM)
H2O : < 0.1 mg/mL

注意: 如下所列的是一些常用的体内动物实验溶解配方，主要用于溶解难溶或不溶于水的产品（水溶度<1 mg/mL）。 建议您先取少量样品进行尝试，如该配方可行，再根据实验需求增加样品量。

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注射用配方1: DMSO : Tween 80： Saline = 10 : 5 : 85 (如： 100 μL DMSO → 50 μL Tween 80 → 850 μL Saline)
*生理盐水/Saline的制备：将0.9g氯化钠/NaCl溶解在100 mL ddH ₂ O中，得到澄清溶液。
注射用配方 2: DMSO : PEG300 ：Tween 80 : Saline = 10 : 40 : 5 : 45 (如： 100 μL DMSO → 400 μL PEG300 → 50 μL Tween 80 → 450 μL Saline)
注射用配方 3: DMSO : Corn oil = 10 : 90 (如： 100 μL DMSO → 900 μL Corn oil)
示例: 以注射用配方 3 (DMSO : Corn oil = 10 : 90) 为例说明, 如果要配制 1 mL 2.5 mg/mL的工作液, 您可以取 100 μL 25 mg/mL 澄清的 DMSO 储备液，加到 900 μL Corn oil/玉米油中, 混合均匀。

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注射用配方 4: DMSO : 20% SBE-β-CD in Saline = 10 : 90 [如：100 μL DMSO → 900 μL (20% SBE-β-CD in Saline)]
*20% SBE-β-CD in Saline的制备（4°C，储存1周）：将2g SBE-β-CD (磺丁基-β-环糊精) 溶解于10mL生理盐水中，得到澄清溶液。
注射用配方 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (如： 500 μL 2-Hydroxypropyl-β-cyclodextrin (羟丙基环胡精)→ 500 μL Saline)
注射用配方 6: DMSO : PEG300 : Castor oil : Saline = 5 : 10 : 20 : 65 (如： 50 μL DMSO → 100 μL PEG300 → 200 μL Castor oil → 650 μL Saline)
注射用配方 7: Ethanol : Cremophor : Saline = 10： 10 : 80 (如： 100 μL Ethanol → 100 μL Cremophor → 800 μL Saline)
注射用配方 8: 溶解于Cremophor/Ethanol (50 : 50), 然后用生理盐水稀释。
注射用配方 9: EtOH : Corn oil = 10 : 90 (如： 100 μL EtOH → 900 μL Corn oil)
注射用配方 10: EtOH : PEG300：Tween 80 : Saline = 10 : 40 : 5 : 45 (如： 100 μL EtOH → 400 μL PEG300 → 50 μL Tween 80 → 450 μL Saline)

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口服配方 1: 悬浮于0.5% CMC Na (羧甲基纤维素钠)
口服配方 2: 悬浮于0.5% Carboxymethyl cellulose (羧甲基纤维素)
示例: 以口服配方 1 (悬浮于 0.5% CMC Na)为例说明, 如果要配制 100 mL 2.5 mg/mL 的工作液, 您可以先取0.5g CMC Na并将其溶解于100mL ddH2O中，得到0.5%CMC-Na澄清溶液；然后将250 mg待测化合物加到100 mL前述 0.5%CMC Na溶液中，得到悬浮液。

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口服配方 3: 溶解于 PEG400 (聚乙二醇400)
口服配方 4: 悬浮于0.2% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 5: 溶解于0.25% Tween 80 and 0.5% Carboxymethyl cellulose (羧甲基纤维素)
口服配方 6: 做成粉末与食物混合

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注意: 以上为较为常见方法，仅供参考， InvivoChem并未独立验证这些配方的准确性。具体溶剂的选择首先应参照文献已报道溶解方法、配方或剂型，对于某些尚未有文献报道溶解方法的化合物，需通过前期实验来确定（建议先取少量样品进行尝试），包括产品的溶解情况、梯度设置、动物的耐受性等。

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请根据您的实验动物和给药方式选择适当的溶解配方/方案：
1、请先配制澄清的储备液(如：用DMSO配置50 或 100 mg/mL母液(储备液));
2、取适量母液，按从左到右的顺序依次添加助溶剂，澄清后再加入下一助溶剂。以 下列配方为例说明 (注意此配方只用于说明，并不一定代表此产品 的实际溶解配方):
10% DMSO → 40% PEG300 → 5% Tween-80 → 45% ddH2O (或 saline);
假设最终工作液的体积为 1 mL, 浓度为5 mg/mL: 取 100 μL 50 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀/澄清；向上述体系中加入50 μL Tween-80，混合均匀/澄清；然后继续加入450 μL ddH2O (或 saline)定容至 1 mL；
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