乳糜微粒
医学
极低密度脂蛋白
脂蛋白
脂蛋白脂酶
中密度脂蛋白
甘油三酯
载脂蛋白B
载脂蛋白E
肝脂肪酶
内科学
内分泌学
生物化学
生物
胆固醇
脂肪组织
疾病
标识
DOI:10.1093/eurheartj/ehab890
摘要
Metabolic choke points are shown at which apolipoprotein (apo) C-III—depicted in two-dimensional semi-circular form—probably affects triglyceride (TG)-rich lipoprotein metabolism. Circled plus (+) and minus (−) signs indicate metabolic steps that apo C-III either promotes or inhibits, respectively. Starting at the upper left (A), dietary fat from the intestine is packaged into chylomicrons (B), which include apo C-III on their surface; apo C-III may promote chylomicron secretion. On the right, TG of endogenous (i.e. hepatic) origin is packaged into very-low-density lipoprotein (VLDL), whose secretion is almost certainly promoted by apo C-III (E). In the plasma space, apo C-III inhibits: (i) lipoprotein lipase (LPL)—indicated in monomeric cartoon form—by impairing the hydrolysis of chylomicrons (C) into chylomicron remnants (D) and of VLDL (F) into intermediate-density lipoprotein (IDL) (G), which is ultimately remodelled into LDL; and (ii) hepatic uptake of TG-rich remnants (D). Interfering with apo C-III production reverses these effects, i.e. reduces secretion of TG-rich lipoproteins (E), increases hydrolysis of TG-rich lipoproteins by LPL (C and F) and permits hepatic removal of TG-rich remnants (D). Metabolic choke points are shown at which apolipoprotein (apo) C-III—depicted in two-dimensional semi-circular form—probably affects triglyceride (TG)-rich lipoprotein metabolism. Circled plus (+) and minus (−) signs indicate metabolic steps that apo C-III either promotes or inhibits, respectively. Starting at the upper left (A), dietary fat from the intestine is packaged into chylomicrons (B), which include apo C-III on their surface; apo C-III may promote chylomicron secretion. On the right, TG of endogenous (i.e. hepatic) origin is packaged into very-low-density lipoprotein (VLDL), whose secretion is almost certainly promoted by apo C-III (E). In the plasma space, apo C-III inhibits: (i) lipoprotein lipase (LPL)—indicated in monomeric cartoon form—by impairing the hydrolysis of chylomicrons (C) into chylomicron remnants (D) and of VLDL (F) into intermediate-density lipoprotein (IDL) (G), which is ultimately remodelled into LDL; and (ii) hepatic uptake of TG-rich remnants (D). Interfering with apo C-III production reverses these effects, i.e. reduces secretion of TG-rich lipoproteins (E), increases hydrolysis of TG-rich lipoproteins by LPL (C and F) and permits hepatic removal of TG-rich remnants (D).
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