Cohn J S, Fidge N H, Nestel P J
Am J Physiol. 1985 Sep;249(3 Pt 1):G369-76. doi: 10.1152/ajpgi.1985.249.3.G369.
The initial tissue distribution of high-density lipoprotein (HDL) was studied in the rat. Specific tissue-space measurements, calculated as the difference between HDL and albumin uptake in a tissue, 10 min after injecting radiolabeled lipoprotein, were taken to represent specific binding of HDL. Rat HDL (rHDL) and human HDL3 (hHDL3) were labeled directly with 125I or with prelabeled 125I-apolipoprotein A-I (125I-apoA-I). Specific tissue spaces were demonstrated for the liver and adrenals but not for spleen, jejunum, ileum, colon, muscle, or adipose tissue. The kidney showed a specific HDL space only when 125I-apoA-I-rHDL was injected. The adrenals bound rHDL to a greater extent than hHDL3, and the liver also bound from three to five times more rHDL than hHDL3. In male and female rats the liver accounted for about two-thirds of total HDL bound. Significantly more HDL was bound by adrenals of female than by male rats, but the reverse occurred for liver and kidney. The greater hepatic binding of HDL in males compared to females was consistent with measurements of HDL flux, calculated from constant infusions of labeled HDL; the fractional clearance of 125I-apoA-I-rHDL was 572 +/- 13 microliter plasma X h-1 X 100 g body wt-1 in males and 466 +/- 19 microliter plasma X h-1 X 100 g body wt-1 in females (P less than 0.01). Tissue-space measurements with 125I-rHDL were not affected by age. Fasting for 48 h increased HDL binding by liver but not by adrenals.(ABSTRACT TRUNCATED AT 250 WORDS)
在大鼠中研究了高密度脂蛋白(HDL)的初始组织分布。通过计算放射性标记脂蛋白注射10分钟后组织中HDL与白蛋白摄取量的差值得出特定组织间隙测量值,以此代表HDL的特异性结合。大鼠HDL(rHDL)和人HDL3(hHDL3)直接用125I或预先标记的125I - 载脂蛋白A - I(125I - apoA - I)进行标记。结果表明肝脏和肾上腺存在特异性组织间隙,而脾脏、空肠、回肠、结肠、肌肉或脂肪组织则没有。仅在注射125I - apoA - I - rHDL时,肾脏显示出特异性HDL间隙。肾上腺对rHDL的结合程度高于hHDL3,肝脏对rHDL的结合量也比hHDL3多三到五倍。在雄性和雌性大鼠中,肝脏约占结合的总HDL的三分之二。雌性大鼠肾上腺结合的HDL明显多于雄性大鼠,但肝脏和肾脏的情况则相反。与雌性相比,雄性大鼠肝脏对HDL的结合量更高,这与通过持续输注标记HDL计算得出的HDL通量测量结果一致;雄性大鼠中125I - apoA - I - rHDL的分数清除率为572±13微升血浆×小时-1×100克体重-1,雌性大鼠为466±19微升血浆×小时-1×100克体重-1(P<0.01)。用125I - rHDL进行的组织间隙测量不受年龄影响。禁食48小时会增加肝脏对HDL的结合,但不会增加肾上腺对HDL的结合。(摘要截选至250字)