Literature DB >> 2230708

Absorbance signals from resting frog skeletal muscle fibers injected with the pH indicator dye, phenol red.

S M Baylor1, S Hollingworth.   

Abstract

Singly dissected twitch fibers from frog muscle were studied on an optical bench apparatus after micro-injection with the pH indicator dye, phenol red. Dye-related absorbances in myoplasm, denoted by A0(lambda) and A90(lambda), were estimated as a function of wavelength lambda (450 nm less than or equal to lambda less than or equal to 640 nm) with light polarized parallel (0 degrees) and perpendicular (90 degrees) to the fiber axis respectively. At all lambda, A0(lambda) was slightly greater than A90(lambda), indicating that some of the phenol red molecules were bound to oriented structures accessible to myoplasm. The phenol red "isotropic" signal, [A0(lambda) + 2A90(lambda)]/3, a quantity equal to the average absorbance of all the dye molecules independent of their orientation, had a spectral shape that was red-shifted by approximately 10 nm in comparison with in vitro dye calibration curves measured in 140 mM KCl. The red-shifted spectrum also indicates that some phenol red molecules were bound in myoplasm. A quantitative estimate of indicator binding was obtained from measurements of the dye's apparent diffusion constant in myoplasm, denoted by Dapp. The small value of Dapp, 0.37 x 10(-6) cm2 s-1 (at 16 degrees C), can be explained if approximately 80% of the dye was bound to myoplasmic sites of low mobility. To estimate the apparent myoplasmic pH, denoted by pHapp, the isotropic absorbance of phenol red was fitted by in vitro calibration spectra. pHapp was found to be independent of dye concentration (0.2-2 mM), but varied widely (range, 6.8-7.5; mean value, 7.17) among fibers judged from functional characteristics to be normal. When fibers were subjected to acid or alkaline loads by exposure to Ringer's solution containing, respectively, dissolved CO2 or NH3, the changes in pHapp were in agreement with those expected from pH micro-electrode studies. It is concluded that in spite of the several indications for the presence of bound phenol red inside muscle cells, the pHapp signal from the indicator is useful for monitoring changes in myoplasmic pH in response to physiological and pharmacological manipulations.

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Year:  1990        PMID: 2230708      PMCID: PMC2229001          DOI: 10.1085/jgp.96.3.449

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  11 in total

1.  The impact of cell culture equipment on energy loss.

Authors:  Lleucu B Davies; Michael N Kiernan; Joanna C Bishop; Catherine A Thornton; Gareth Morgan
Journal:  Lasers Med Sci       Date:  2013-04-09       Impact factor: 3.161

2.  Fluorescence signals from the Mg2+/Ca2+ indicator furaptra in frog skeletal muscle fibers.

Authors:  M Konishi; N Suda; S Kurihara
Journal:  Biophys J       Date:  1993-01       Impact factor: 4.033

3.  Properties of tri- and tetracarboxylate Ca2+ indicators in frog skeletal muscle fibers.

Authors:  M Zhao; S Hollingworth; S M Baylor
Journal:  Biophys J       Date:  1996-02       Impact factor: 4.033

4.  AM-loading of fluorescent Ca2+ indicators into intact single fibers of frog muscle.

Authors:  M Zhao; S Hollingworth; S M Baylor
Journal:  Biophys J       Date:  1997-06       Impact factor: 4.033

5.  Simulation of calcium sparks in cut skeletal muscle fibers of the frog.

Authors:  W K Chandler; S Hollingworth; S M Baylor
Journal:  J Gen Physiol       Date:  2003-03-17       Impact factor: 4.086

6.  How source content determines intracellular Ca2+ release kinetics. Simultaneous measurement of [Ca2+] transients and [H+] displacement in skeletal muscle.

Authors:  Gonzalo Pizarro; Eduardo Ríos
Journal:  J Gen Physiol       Date:  2004-09       Impact factor: 4.086

7.  Use of fura red as an intracellular calcium indicator in frog skeletal muscle fibers.

Authors:  N Kurebayashi; A B Harkins; S M Baylor
Journal:  Biophys J       Date:  1993-06       Impact factor: 4.033

8.  Valinomycin and excitation-contraction coupling in skeletal muscle fibres of the frog.

Authors:  P C Pape; M Konishi; S M Baylor
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

9.  Myoplasmic calcium transients in intact frog skeletal muscle fibers monitored with the fluorescent indicator furaptra.

Authors:  M Konishi; S Hollingworth; A B Harkins; S M Baylor
Journal:  J Gen Physiol       Date:  1991-02       Impact factor: 4.086

10.  Myoplasmic calcium transients monitored with purpurate indicator dyes injected into intact frog skeletal muscle fibers.

Authors:  M Konishi; S M Baylor
Journal:  J Gen Physiol       Date:  1991-02       Impact factor: 4.086

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