Indigo Leaves-Induced Pulmonary Arterial Remodeling without Right Ventricular Hypertrophy in Rats

被引:0
|
作者
Tsunematsu, Honoka [1 ]
Imanishi, Masaki [1 ]
Uemura, Yuka [1 ]
Higaki, Yoshiya [1 ]
Morisaki, Miyu [1 ]
Katsura, Akari [1 ]
Miyamoto, Licht [2 ]
Funamoto, Masafumi [3 ]
Ichimura-Shimizu, Mayuko [4 ]
Horinouchi, Yuya [5 ]
Ikeda, Yasumasa [3 ]
Tsuneyama, Koichi [4 ]
Tsuchiya, Koichiro [1 ]
机构
[1] Tokushima Univ, Grad Sch Biomed Sci, Dept Med Pharmacol, 1-78-1 Shoumachi, Tokushima 7708505, Japan
[2] Kanagawa Inst Technol, Fac Hlth & Med Sci, Dept Nutr & Life Sci, Lab Pharmacol & Food Sci, 1030 Shimoogino, Atsugi, Kanagawa 2430292, Japan
[3] Tokushima Univ, Grad Sch Biomed Sci, Dept Pharmacol, 3-18-15 Kuramoto Cho, Tokushima 7708503, Japan
[4] Tokushima Univ, Grad Sch Biomed Sci, Dept Pathol & Lab Med, 3-18-15 Kuramoto Cho, Tokushima 7708503, Japan
[5] Tokushima Bunri Univ, Fac Pharmaceut Sci, Dept Pharmaceut Care & Clin Pharm, Yamashiro, Tokushima 7708514, Japan
关键词
indigo naturalis; indigo leaf; indican; indoxyl sulfate; pulmonary arterial hypertension; endothelin-1; INDOXYL SULFATE; CELL-PROLIFERATION; UREMIC TOXIN; ENDOTHELIN-1; EXPRESSION; RECEPTOR; NATURALIS; INDICAN; PATHWAY; TISSUE;
D O I
10.1248/bpb.b24-00289
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Indigo naturalis (IN), derived from the leaves of the indigo plant, is a traditional Chinese medicine that has historically been used for its anti-inflammatory properties in the treatment of various diseases, including ulcerative colitis (UC). However, long-term use of IN in UC patients is incontrovertibly associated with the onset of pulmonary arterial hypertension (PAH). To investigate the mechanisms by which IN induces PAH, we focused on the raw material of IN, indigo leaves (IL). Only the condition of long-term chronic (6 months) and high-dose (containing 5% IL in the control diet) administration of IL induced medial thickening in the pulmonary arteries without right ventricular hypertrophy in our rat model. IL administration for a month did not induce pulmonary arterial remodeling but increased endothelin-1 (ET-1) expression levels within endothelial cell (EC) layers in the lungs. Gene Expression Omnibus analysis showed that ET-1 is a key regulator of PAH and that the IL component indican and its metabolite IS induced ET-1 mRNA expression via reactive oxygen species-dependent mechanism. We identified the roles of indican and IS in ET-1 expression in ECs, which were linked to pulmonary arterial remodeling in an animal model.
引用
收藏
页码:1350 / 1359
页数:10
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