Blum J J
Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27706.
J Protozool. 1991 May-Jun;38(3):229-33. doi: 10.1111/j.1550-7408.1991.tb04434.x.
Leishmania major promastigotes were washed and resuspended in an iso-osmotic buffer. The rate of oxidation of 14C-labeled substrates was then measured as a function of osmolality. An acute decrease in osmolality (achieved by adding H2O to the cell suspension) caused an increase in the rates of 14CO2 production from [6-14C]glucose and, to a lesser extent, from [1,(3)-14C]glycerol. An acute increase in osmolality (achieved by adding NaCl, KCl, or mannitol) strongly inhibited the rates of 14CO2 production from [1-14C]alanine,[1-14C]glutamate, and [1,(3)-14C]glycerol. The rates of 14CO2 formation from [1-14C]laurate,[1-14C]acetate, and [2-14C]glucose (all of which form [1-14C]acetyl CoA prior to oxidation) were also inhibited, but less strongly, by increasing osmolality. These data suggest that with increasing osmolality there is an inhibition of mitochondrial oxidative capacity, which could facilitate the increase in alanine pool size that occurs in response to hyper-osmotic stress. Similarly, an increase in oxidative capacity would help prevent a rebuild up of the alanine pool after its rapid loss to the medium in response to hypo-osmotic stress.
硕大利什曼原虫前鞭毛体经洗涤后重悬于等渗缓冲液中。然后测定14C标记底物的氧化速率与渗透压的函数关系。渗透压急剧降低(通过向细胞悬液中加入水来实现)导致[6-14C]葡萄糖以及程度稍低的[1,(3)-14C]甘油产生14CO2的速率增加。渗透压急剧升高(通过加入NaCl、KCl或甘露醇来实现)强烈抑制[1-14C]丙氨酸、[1-14C]谷氨酸和[1,(3)-14C]甘油产生14CO2的速率。[1-14C]月桂酸、[1-14C]乙酸和[2-14C]葡萄糖(所有这些在氧化前均形成[1-14C]乙酰辅酶A)产生14CO2的速率也受到渗透压升高的抑制,但抑制程度较弱。这些数据表明,随着渗透压升高,线粒体氧化能力受到抑制,这可能有助于响应高渗应激时丙氨酸池大小的增加。同样,氧化能力的增加将有助于防止在响应低渗应激时丙氨酸池迅速释放到培养基后其重新积累。