Why the study?
Does the form of apoA-I or the presence of hepatic lipase affect the in vivo metabolism and fractional catabolic rate of apoA-I in rabbits?
Does the form of apoA-I or the presence of hepatic lipase affect the in vivo metabolism and fractional catabolic rate of apoA-I in rabbits?
Hepatic lipase increases the catabolism of apoA-I and reduces the size of alpha-migrating HDLs in vivo, while the fractional catabolic rate of apoA-I is independent of its initial injected form.
Does not support clinical translation; leaves open hepatic lipase effects on human apoA-I metabolism.
OBJECTIVE: Apolipoprotein (apo)A-I exists in 3 forms in plasma: as lipid-free apoA-I, as a component of pre-beta-migrating discoidal high density lipoproteins (HDLs), and as a component of alpha-migrating spherical HDLs. This study investigates (1) the in vivo metabolism of apoA-I in each of these forms and (2) the effects of hepatic lipase (HL) on apoA-I metabolism. METHODS AND RESULTS: Wild-type and HL transgenic rabbits were studied. When lipid-free (125)I-apoA-I and 125I-apoA-I in pre-beta-migrating discoidal reconstituted HDLs (rHDLs) were injected into wild-type rabbits, the label rapidly appeared in alpha-migrating particles and decayed with the same fractional catabolic rate (FCR) as when they were injected as a component of spherical rHDLs. Spherical rHDLs did not change in size when they were injected into wild-type rabbits but were reduced in size in HL transgenic rabbits. The FCR of apoA-I in HL transgenic rabbits was double that in wild-type rabbits. CONCLUSIONS: In vivo, (1) lipid-free apoA-I rapidly incorporates into preexisting alpha-migrating particles, (2) pre-beta-migrating discoidal HDLs are rapidly converted into alpha-migrating HDLs, (3) the FCR of apoA-I is independent of the form in which it is introduced into plasma, and (4) HL reduces the size of alpha-migrating HDLs and increases the rate of catabolism of apoA-I.
No takes yet. Share an insight, caveat, or question.
Kee et al. (2002) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: