CA-45 DISTRIBUTION AND TRANSPORT IN SAPONIN SKINNED VASCULAR SMOOTH-MUSCLE

  • 1 January 1983
    • journal article
    • research article
    • Vol. 225  (1) , 102-111
Abstract
45Ca distribution and transport were studied in chemically skinned strips of caudal artery from Kyoto Wistar rats. Sarcolemmal membranes were made hyperpermeable by exposure for 60 min to solutions containing 0.1 mg/ml of saponin. Skinned helical strips responded with graded contractions to changes in ethylene glycol bis-(.beta.-aminoethyl ether)-N,N''-tetraacetic acid buffered free Ca solutions (10-7 to 10-5 M) and were sensitive to the Mg-ATP concentration. Tissues loaded in the presence of 10-7 M Ca contracted in response to 10 mM caffeine. The strips apparently are skinned and possess a functional regulatory and contractile system, and an intact Ca sequestering system. 45Ca distributes in 3 compartments in skinned caudal artery strips. The Ca contents of 2 components are linear functions of the Ca-ethylene glycol bis-(.beta.-aminoethyl ether)-N,N''-tetraacetic acid concentration and desaturate at rapid rates. They correspond to the extracellular and cytoplasmic spaces. A significantly smaller component releases Ca at comparatively slower rates. 45Ca uptake by the slow component consists of an ATP-dependent and an ATP-independent fraction. The 45Ca content of the ATP-dependent fraction is a function of the free Ca concentration and is independent of the Ca-ethylene glycol bis-(.beta.-aminoethyl ether)-N,N''-tetraacetic acid concentration. Its content was enhanced by oxalate and was abolished by Triton X-100 skinning solutions. The ATP-independent component was not affected by Triton X-100 skinning and may represent Ca binding to cytoplasmic molecules and structures. The sequestered Ca was released with caffeine or Ca but not by epinephrine. The sarcoplasmic reticulum and mitochondria of vascular smooth muscle strips skinned with saponin apparently retain their functional integrity after saponin skinning.

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