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Publication : Organ Weights in NPC1 Mutant Mice Partly Normalized by Various Pharmacological Treatment Approaches.

First Author  Antipova V Year  2022
Journal  Int J Mol Sci Volume  24
Issue  1 PubMed ID  36614015
Mgi Jnum  J:332613 Mgi Id  MGI:7426684
Doi  10.3390/ijms24010573 Citation  Antipova V, et al. (2022) Organ Weights in NPC1 Mutant Mice Partly Normalized by Various Pharmacological Treatment Approaches. Int J Mol Sci 24(1)
abstractText  Niemann-Pick Type C1 (NPC1, MIM 257220) is a rare, progressive, lethal, inherited autosomal-recessive endolysosomal storage disease caused by mutations in the NPC1 leading to intracellular lipid storage. We analyzed mostly not jet known alterations of the weights of 14 different organs in the BALB/cNctr-Npc1(m1N)/-J Jackson Npc1 mice in female and male Npc1(+/+) and Npc1(-/-) mice under various treatment strategies. Mice were treated with (i) no therapy, (ii) vehicle injection, (iii) a combination of miglustat, allopregnanolone, and 2-hydroxypropyl-ss-cyclodextrin (HPssCD), (iv) miglustat, and (v) HPssCD alone starting at P7 and repeated weekly throughout life. The 12 respective male and female wild-type mice groups were evaluated in parallel. In total, 351 mice (176 Npc1(+/+), 175 Npc1(-/-)) were dissected at P65. In both sexes, the body weights of None and Sham Npc1(-/-) mice were lower than those of respective Npc1(+/+) mice. The influence of the Npc1 mutation and/or sex on the weights of various organs, however, differed considerably. In males, Npc1(+/+) and Npc1(-/-) mice had comparable absolute weights of lungs, spleen, and adrenal glands. In Npc1(-/-) mice, smaller weights of hearts, livers, kidneys, testes, vesicular, and scent glands were found. In female Npc1(-/-) mice, ovaries, and uteri were significantly smaller. In Npc1(-/-) mice, relative organ weights, i.e., normalized with body weights, were sex-specifically altered to different extents by the different therapies. The combination of miglustat, allopregnanolone, and the sterol chelator HPssCD partly normalized the weights of more organs than miglustat or HPssCD mono-therapies.
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