Chin E R, Green H J, Grange F, Mercer J D, O'Brien P J
Department of Kinesiology, University of Waterloo, Ontario, Canada.
Mol Cell Biochem. 1994 Oct 12;139(1):41-52. doi: 10.1007/BF00944202.
A multiple measurement system for assessing sarcoplasmic reticulum (SR) Ca(++)-ATPase activity and Ca(++)-uptake was used to examine the effects of SR fractionation and quick freezing on rat white (WG) and red (RG) gastrocnemius muscle. In vitro measurements were performed on whole muscle homogenates (HOM) and crude microsomal fractions (CM) enriched in SR vesicles before and after quick freezing in liquid nitrogen. Isolation of the CM fraction resulted in protein yields of 0.96 +/- 0.1 and 0.99 +/- 0.1 mg/g in WG and RG, respectively. The percent Ca(++)-ATPase recovery for CM compared to HOM was 14.5% (WG) and 10.1% (RG). SR Ca(++)-activated Ca(++)-ATPase activity was not affected by quick freezing of HOM or CM, but basal ATPase was reduced (P < 0.05) in frozen HOM (5.12 +/- 0.18-3.98 +/- 0.20 mole/g tissue/min in WG and from 5.39 +/- 0.20-4.48 +/- 0.24 mumole/g tissue/min in RG). Ca(++)-uptake was measured at a range of physiological free [Ca++] using the Ca++ fluorescent dye Indo-1. Maximum Ca(++)-uptake rates when corrected for initial [Ca++]f were not altered in HOM or CM by quick freezing but uptake between 300 and 400nM free Ca++ was reduced (P < 0.05) in quick frozen HOM (1.30 +/- 0.1-0.66 +/- 0.1 mumole/g tissue/min in WG and 1.04 +/- 0.2-0.60 +/- 0.1 mumole/g tissue/min in RG). Linear correlations between Ca(++)-uptake and Ca(++)-ATPase activity measured in the presence of the Ca++ ionophore A23187 were r = +0.25, (P < 0.05) and r = +0.74 (P < 0.05) in HOM and CM preparations, respectively, and were not altered by freezing. The linear relationships between HOM and CM maximum Ca(++)-uptake (r = +0.44, P < 0.05) and between HOM and CM Ca(++)-ATPase activity (r = +0.34, P < 0.05) were also not altered by tissue freezing. These data suggest that alterations in maximal SR Ca(++)-uptake function and maximal Ca(++)-ATPase activity may be measured in both HOM and CM fractions following freezing and short term storage.
采用一种用于评估肌浆网(SR)Ca(++)-ATP酶活性和Ca(++)摄取的多重测量系统,来检测SR分级分离和快速冷冻对大鼠白色(WG)和红色(RG)腓肠肌的影响。在液氮中快速冷冻前后,对富含SR囊泡的全肌肉匀浆(HOM)和粗微粒体组分(CM)进行体外测量。CM组分的分离使得WG和RG中的蛋白质产量分别为0.96±0.1和0.99±0.1mg/g。与HOM相比,CM的Ca(++)-ATP酶回收率在WG中为14.5%,在RG中为10.1%。SR Ca(++)激活的Ca(++)-ATP酶活性不受HOM或CM快速冷冻的影响,但冷冻后的HOM中基础ATP酶活性降低(P<0.05)(WG中从5.12±0.18降至3.98±0.20微摩尔/克组织/分钟,RG中从5.39±0.20降至4.48±0.24微摩尔/克组织/分钟)。使用Ca++荧光染料Indo-1在一系列生理游离[Ca++]条件下测量Ca(++)摄取。校正初始[Ca++]f后的最大Ca(++)摄取率在HOM或CM中不受快速冷冻的影响,但快速冷冻后的HOM中300至400nM游离Ca++之间的摄取量降低(P<0.05)(WG中从1.30±0.1降至0.66±0.1微摩尔/克组织/分钟,RG中从1.04±0.2降至0.60±0.1微摩尔/克组织/分钟)。在Ca++离子载体A23187存在下测量的Ca(++)摄取与Ca(++)-ATP酶活性之间的线性相关性在HOM和CM制剂中分别为r = +0.25(P<0.05)和r = +0.74(P<0.05),且不受冷冻影响。HOM和CM最大Ca(++)摄取之间(r = +0.44,P<0.05)以及HOM和CM Ca(++)-ATP酶活性之间(r = +0.34,P<0.05)的线性关系也不受组织冷冻的影响。这些数据表明,在冷冻和短期储存后,可在HOM和CM组分中测量最大SR Ca(++)摄取功能和最大Ca(++)-ATP酶活性的变化。