Evidence map›Paper›PMID 26404254›Full record

ArticleInternational journal of molecular sciences2015

Weekly Treatment of 2-Hydroxypropyl-β-cyclodextrin Improves Intracellular Cholesterol Levels in LDL Receptor Knockout Mice.

Sofie M A Walenbergh, Tom Houben, Tim Hendrikx, Mike L J Jeurissen, Patrick J van Gorp, Nathalie Vaes, Steven W M Olde Damink, Fons Verheyen, Ger H Koek, Dieter Lütjohann and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Organ Weights inInternational journal of molecular sciences · 2022
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Inflammation and Metabolic Complications in HIV.Current HIV/AIDS reports · 2018
    Review
  10. NAFLD: Is There Anything New under the Sun?International journal of molecular sciences · 2017
    Article
  11. Review
  12. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 4 countries.

Sofie M A WalenberghDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. s.walenbergh@maastrichtuniversity.nl.
Tom HoubenDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. tom.houben@maastrichtuniversity.nl.
Tim HendrikxDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. t.hendrikx@maastrichtuniversity.nl.
Mike L J JeurissenDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. m.jeurissen@maastrichtuniversity.nl.
Patrick J van GorpDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. p.vangorp@maastrichtuniversity.nl.
Nathalie VaesDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. n.vaes@maastrichtuniversity.nl.
Steven W M Olde DaminkDepartment of General Surgery, Maastricht University, Maastricht 6229ER, The Netherlands. steven.oldedamink@maastrichtuniversity.nl.
Fons VerheyenDepartment of Molecular Cell Biology and Electron Microscopy, Maastricht University, Maastricht 6229ER, The Netherlands. f.verheyen@maastrichtuniversity.nl.
Ger H KoekDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Maastricht University Medical Center (MUMC), Maastricht 6202AZ, The Netherlands. gh.koek@mumc.nl.
Dieter LütjohannInstitute of Clinical Chemistry and Clinical Pharmacology, University of Bonn, Bonn D-53105, Germany. dieter.luetjohann@ukb.uni-bonn.de.
Alena GrebeInstitute of Innate Immunity, University Hospital, University of Bonn, Bonn D-53127, Germany. alena.grebe@uni-bonn.de.
Eicke LatzInstitute of Innate Immunity, University Hospital, University of Bonn, Bonn D-53127, Germany. eicke.latz@umassmed.edu.
Ronit Shiri-SverdlovDepartment of Molecular Genetics, School of Nutrition and Translational Research in Metabolism (NUTRIM), Maastricht University, Maastricht 6229ER, The Netherlands. r.sverdlov@maastrichtuniversity.nl.
Maastricht University · NLMaastricht University Medical Centre · NLThe Royal Free Hospital · GBUniversity Hospital Bonn · DEUniversity of Bonn · DEUniversity of Massachusetts Chan Medical School · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, the importance of lysosomes in the context of the metabolic syndrome has received increased attention. Increased lysosomal cholesterol storage and cholesterol crystallization inside macrophages have been linked to several metabolic diseases, such as atherosclerosis and non-alcoholic fatty liver disease (NAFLD). Two-hydroxypropyl-β-cyclodextrin (HP-B-CD) is able to redirect lysosomal cholesterol to the cytoplasm in Niemann-Pick type C1 disease, a lysosomal storage disorder. We hypothesize that HP-B-CD ameliorates liver cholesterol and intracellular cholesterol levels inside Kupffer cells (KCs). Hyperlipidemic low-density lipoprotein receptor knockout (Ldlr(-/-)) mice were given weekly, subcutaneous injections with HP-B-CD or control PBS. In contrast to control injections, hyperlipidemic mice treated with HP-B-CD demonstrated a shift in intracellular cholesterol distribution towards cytoplasmic cholesteryl ester (CE) storage and a decrease in cholesterol crystallization inside KCs. Compared to untreated hyperlipidemic mice, the foamy KC appearance and liver cholesterol remained similar upon HP-B-CD administration, while hepatic campesterol and 7α-hydroxycholesterol levels were back increased. Thus, HP-B-CD could be a useful tool to improve intracellular cholesterol levels in the context of the metabolic syndrome, possibly through modulation of phyto- and oxysterols, and should be tested in the future. Additionally, these data underline the existence of a shared etiology between lysosomal storage diseases and NAFLD.

Indexed as

2-Hydroxypropyl-beta-cyclodextrinAnimalsbeta-CyclodextrinsCholesterolDisease Models, AnimalDrug Administration ScheduleHyperlipidemiasInjections, SubcutaneousKupffer CellsLiverLysosomesMiceMice, KnockoutReceptors, LDL2-Hydroxypropyl-beta-cyclodextrinbeta-CyclodextrinsCholesterolReceptors, LDLcyclodextrinelectron microscopylysosomesmetabolic syndromeNAFLD

Identifiers

PMID26404254
PMCPMC4613241
OpenAlexW2136998170

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.