Co-treatment with probucol does not improve lung pathology in hydroxypropyl-β-cyclodextrin-treated Npc1−/− mice

被引:0
|
作者
Robert P. Erickson
Ivan A. Borbon
机构
[1] University of Arizona College of medicine,Department of pediatrics
来源
Journal of Applied Genetics | 2019年 / 60卷
关键词
Niemann-pick C1 disease; Mouse model; Probucol; Hydroxypropyl-β-cyclodextrin; Pulmonary function; Cholesterol storage;
D O I
暂无
中图分类号
学科分类号
摘要
We previously reported the altered pulmonary function and pathology found in the mouse model of infantile Niemann-Pick C1 disease, the Npc1−/− mouse. Despite its salutary properties on brain and liver parameters, we did not find efficacious effects of hydroxypropyl-β-cyclodextrin (HPBCD) on pulmonary pathology. Since we had previously shown the beneficial effects of probucol on the somatic phenotype in the Npc1−/− mice, we have now studied the effects of combined therapy with HPBCD and probucol on the lung with mostly negative results. Body weight and lung weight for body weight were increased in parallel while inspiratory capacity for body weight was markedly decreased. Other physical, biochemical, and pulmonary function parameters were not much changed. There were trends towards improved lung elastance (p = 0.09) and compliance (p = 0.07).
引用
收藏
页码:175 / 178
页数:3
相关论文
共 4 条
  • [1] Co-treatment with probucol does not improve lung pathology in hydroxypropyl--cyclodextrin-treated Npc1-/- mice
    Erickson, Robert P.
    Borbon, Ivan A.
    JOURNAL OF APPLIED GENETICS, 2019, 60 (02) : 175 - 178
  • [2] NPC1 Deficiency in Mice is Associated with Fetal Growth Restriction, Neonatal Lethality and Abnormal Lung Pathology
    Rodriguez-Gil, Jorge L.
    Watkins-Chow, Dawn E.
    Baxter, Laura L.
    Yokoyama, Tadafumi
    Zerfas, Patricia M.
    Starost, Matthew F.
    Gahl, William A.
    Malicdan, May Christine V.
    Porter, Forbes D.
    Platt, Frances M.
    Pavan, William J.
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (01)
  • [3] Pulmonary function and pathology in hydroxypropyl-beta-cyclodextin-treated and untreated Npc1-/- mice
    Muralidhar, Akshay
    Borbon, Ivan A.
    Esharif, Dyadin M.
    Ke, Wangjing
    Manacheril, Rinu
    Daines, Michael
    Erickson, Robert P.
    MOLECULAR GENETICS AND METABOLISM, 2011, 103 (02) : 142 - 147
  • [4] Delineation of metabolic responses of Npc1-/-nih mice lacking the cholesterol-esterifying enzyme SOAT2 to acute treatment with 2-hydroxypropyl-β-cyclodextrin
    Ramirez, Charina M.
    Taylor, Anna M.
    Lopez, Adam M.
    Repa, Joyce J.
    Turley, Stephen D.
    STEROIDS, 2020, 164