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Holzmann, C; Witt, M; Rolfs, A; Antipova, V; Wree, A.
Gender-Specific Effects of Two Treatment Strategies in a Mouse Model of Niemann-Pick Disease Type C1
INT J MOL SCI. 2021; 22(5): 2539 Doi: 10.3390/ijms22052539 [OPEN ACCESS]
Web of Science PubMed PUBMED Central FullText FullText_MUG

 

Leading authors Med Uni Graz
Antipova Veronica Alexandra
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Abstract:
In a mouse model of Niemann-Pick disease type C1 (NPC1), a combination therapy (COMBI) of miglustat (MIGLU), the neurosteroid allopregnanolone (ALLO) and the cyclic oligosaccharide 2-hydroxypropyl-β-cyclodextrin (HPßCD) has previously resulted in, among other things, significantly improved motor function. The present study was designed to compare the therapeutic effects of the COMBI therapy with that of MIGLU or HPßCD alone on body and brain weight and the behavior of NPC1-/- mice in a larger cohort, with special reference to gender differences. A total of 117 NPC1-/- and 123 NPC1+/+ mice underwent either COMBI, MIGLU only, HPßCD only, or vehicle treatment (Sham), or received no treatment at all (None). In male and female NPC1-/- mice, all treatments led to decreased loss of body weight and, partly, brain weight. Concerning motor coordination, as revealed by the accelerod test, male NPC1-/- mice benefited from COMBI treatment, whereas female mice benefited from COMBI, MIGLU, and HPßCD treatment. As seen in the open field test, the reduced locomotor activity of male and female NPC1-/- mice was not significantly ameliorated in either treatment group. Our results suggest that in NPC1-/- mice, each drug treatment scheme had a beneficial effect on at least some of the parameters evaluated compared with Sham-treated mice. Only in COMBI-treated male and female NPC+/+ mice were drug effects seen in reduced body and brain weights. Upon COMBI treatment, the increased dosage of drugs necessary for anesthesia in Sham-treated male and female NPC1-/- mice was almost completely reduced only in the female groups.
Find related publications in this database (using NLM MeSH Indexing)
1-Deoxynojirimycin - analogs & derivatives, pharmacology
2-Hydroxypropyl-beta-cyclodextrin - pharmacology
Animals - administration & dosage
Cyclodextrins - pharmacology
Disease Models, Animal - administration & dosage
Drug Therapy, Combination - methods
Female - administration & dosage
Male - administration & dosage
Mice - administration & dosage
Mice, Inbred BALB C - administration & dosage
Niemann-Pick Disease, Type C - drug therapy
Pregnanolone - pharmacology

Find related publications in this database (Keywords)
NPC1
mouse
lipid storage disorder
treatment
miglustat
2-hydroxypropyl-β -cyclodextrin
allopregnanolone
body weight
brain weight
anesthesia
behavior
accelerod test
open field test
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