• No results found

University of Groningen Disturbed vitamin A metabolism in chronic liver disease and relevance for therapy Saeed, Ali

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Disturbed vitamin A metabolism in chronic liver disease and relevance for therapy Saeed, Ali"

Copied!
2
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Disturbed vitamin A metabolism in chronic liver disease and relevance for therapy Saeed, Ali

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date: 2019

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Saeed, A. (2019). Disturbed vitamin A metabolism in chronic liver disease and relevance for therapy. University of Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

PROPOSITIONS

Stellingen behorende bij het proefschrift:

Disturbed vitamin A metabolism in chronic liver disease and relevance for therapy

1. The fact that the liver contains multiple retinyl ester hydrolases (PNPLA3, ATGL, HSL) and only one enzyme that esterifies retinol (LRAT) indicates that vitamin A release from the liver is evolutionary more important than vitamin A storage. (This

thesis)

2. Hepatic vitamin A storage is much more sensitive to metabolic disease and therapies as compared to circulatory vitamin A levels, which should also be included in the clinical assessment of systemic and tissue vitamin A deficiency (VAD). (This thesis)

3. Non-alcoholic fatty liver disease (NAFLD) is not associated with systemic vitamin A deficiency, but impaired vitamin A metabolism. (This thesis)

4. Hepatocytes are the dominant vitamin A-storing cells in NAFLD, not the hepatic stellate cells. (This thesis)

5. The accurate quantification of retinyl esters in fatty livers is highly dependent on the lipid extraction method, especially in the tissue from fatty liver. (This thesis) 6. Glycogen Storage Disease Ia is associated with impaired vitamin A metabolism

that may contribute to disease-associated symptoms, such as hepatic steatosis and osteoporosis. (This thesis)

7. Low serum retinol levels in patients with NAFLD should not be treated with over-the-counter oral vitamin A supplements. (This thesis)

8. FXR-targeted therapies reduce hepatic vitamin A storage and show the ability to correct the accumulation of hepatic vitamin A in NAFLD. (This thesis)

9. It is not funny that, by adapting to a Western diet, I turned obese (gained 22 kg) while searching for new therapeutic targets against obesity and NAFLD.

10. Science generates more questions in the attempt to answer a few.

11. Critique is a great tool that works best if someone applies it at his/herself. 12. To achieve a goal needs motivation, focus, patience and hard-but-smart work. 13. Education is the key to eradicate hate in the world spread by our political leaders.

Referenties

GERELATEERDE DOCUMENTEN

Chapter 5: Hepatic vitamin A metabolism is disturbed in mice with Non-Alcoholic Fatty Liver Disease leading to vitamin A accumulation in

Moreover, non-alcoholic fatty liver disease (NAFLD) and related pathologies like obesity, type 2 diabetes and metabolic syndrome, have repeatedly been shown to be

Via nuclear receptors, vitamin A-metabolites directly regulate bile acid synthesis and transport, while bile acids control expression of genes involved in vitamin

Hepatic expression was most dominant in the portal tree fractions and purified qHSC, while much lower levels were observed in hepatocytes, both in rat and human liver

Moreover, PNPLA3 expression is induced upon HSC activation and the PNPLA3-I148M variant further promotes fibrogenic features of HSC, including enhanced proliferation,

Faber, Disturbed Vitamin A Metabolism in Non-Alcoholic Fatty Liver Disease (NAFLD), Nutrients.. Mice were fed a chow diet or HFD diet for 12 weeks and analyzed

export in L-G6pc -/- fasted-mice. Transcript analyses suggest that the balance between vitamin A storage/retinol synthesis in the liver shifts to retinol synthesis in L-G6pc -/-

mRNA and protein levels of FXR targets and vitamin A metabolizing factors. B) Hepatic retinyl palmitate levels were significantly reduced in OCA-treated mice, while hepatic