Mersmann H J
J Anim Sci. 1986 Sep;63(3):757-69. doi: 10.2527/jas1986.633757x.
Rates of adipose tissue lipid metabolism in vitro are often measured to evaluate the function in vivo of metabolic pathways and thus appraise the accretion or loss of depot fat. This study directly addressed the comparison of degradative metabolism in vitro and in vivo. The concentrations of plasma free-fatty-acids and blood-glycerol as putative representatives of lipolysis in vivo and the lipolytic rate in adipose tissue in vitro obtained at the time of blood sampling were both measured in the same pig. Concentrations of plasma free-fatty-acids and blood-glycerol were increased or decreased by infusion of the norepinephrine analog, isoproterenol or by infusion of the adrenergic antagonist, propranolol, respectively. Although lipolytic rates and sensitivity to isoproterenol in vitro changed during some acute hormonal manipulations of the pig, the modulation in vitro was usually small relative to the large changes observed in plasma free-fatty-acid and blood-glycerol concentrations. Some of the subtle changes in vitro may reflect biological responses to hormone infusion, e.g., desensitization of the response to adrenergic agonists, but the magnitude of rate changes in vitro negates prediction of the rates in vivo from rates in vitro. Extrapolation of lipolytic rates in vitro and several adipose tissue anabolic rates obtained from the literature indicate the improbability for prediction of rates and degree of fat accretion in pigs from metabolic rates in vitro.
体外脂肪组织脂质代谢率常被用来评估体内代谢途径的功能,从而评估储存脂肪的增减情况。本研究直接探讨了体外和体内降解代谢的比较。在同一头猪身上,同时测量了作为体内脂肪分解假定代表的血浆游离脂肪酸和血液甘油的浓度,以及采血时体外脂肪组织的脂肪分解率。分别通过输注去甲肾上腺素类似物异丙肾上腺素或输注肾上腺素能拮抗剂普萘洛尔来升高或降低血浆游离脂肪酸和血液甘油的浓度。尽管在对猪进行一些急性激素处理期间,体外脂肪分解率和对异丙肾上腺素的敏感性发生了变化,但相对于血浆游离脂肪酸和血液甘油浓度的大幅变化,体外调节通常较小。体外的一些细微变化可能反映了对激素输注的生物学反应,例如对肾上腺素能激动剂反应的脱敏,但体外速率变化的幅度否定了从体外速率预测体内速率的可能性。根据文献中获得的体外脂肪分解率和几种脂肪组织合成代谢率进行推断,表明从体外代谢率预测猪的脂肪沉积速率和程度是不太可能的。