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Model 300c

Manufactured by Aurora Scientific

The Model 300C is a laboratory instrument designed to measure force and displacement. It features a high-resolution load cell and a precision linear actuator for accurate and reliable measurements.

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3 protocols using model 300c

1

Diaphragm Muscle Contractility Measurement

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The diaphragm strip measurement began with whole-tissue removal while the mouse was under anesthesia. In a dissection bath (136.5 mM NaCl, 5 mM KCl, 1.8 mM CaCl2, 0.5 mM MgCl2, 0.4 mM NaH2PO4, and 11.9 mM NaHCO3), sutures were tied around both ends of a small strip cut along the myofibers of the diaphragm. The strip was placed in a bath (121 mM NaCl, 5 mM KCl, 1.8 mM CaCl2, 0.5 mM MgCl2, 0.4 mM NaH2PO4, 24 mM NaHCO3, and 5.5 mM glucose), and the sutures were tied to the servomotor (model 300-C, Aurora Scientific) and force transducer. A similar procedure as for the TA muscle strength assay was used, with the stimulation voltage and then muscle length adjusted for maximum isomeric twitch force, and the TA length was measured (L0). Tetanus (the point at which maximum tension is generated) was measured at increasing stretch of L0: 0%, 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, and 45%. The signal output of the force transducer was displayed on a storage oscilloscope (Tektronix model 5111) coupled to a microcomputer used for data acquisition and storage.
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2

Isolated Ventricular Trabeculae Contractility

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Thin, unbranched, and intact trabeculae were carefully dissected from the right ventricular wall and mounted between a force transducer (Cambridge Technology, model 400A) and a length-controlling motor (Aurora Scientific, model 300C). Each end of the trabecula was sutured to custom arms attached to the motor and force transducer made from 22-gauge needles. The trabecula was then submerged in a custom experimental chamber that was continuously perfused with modified Krebs buffer (1.8 mM CaCl2) at 30°C. Twitches were elicited by field stimulation with custom platinum plate electrodes at 1 Hz with oscillating polarity. Sarcomere length (SL) was set to 2.0 μm using an inverted stereomicroscope with a ×40 dry objective lens and a ×10 eyepiece. If sarcomeres could not be seen for direct measurement (e.g., if the trabecula was too thick), then an SL of 2.0 μm was assumed to be at trabecula slack length (the length of the trabecula at the onset of passive T development). Trabeculae were allowed to pace at 1 Hz for approximately 20 minutes at SL 2.0 μm (and 30°C) and then stretched to SL 2.3 μm for data acquisition.
Continuous twitch T-time traces were recorded using custom LabView software at a sampling rate of 1 kHz and were analyzed using custom code with MATLAB software (version 2018a, The MathWorks).
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3

Muscle Fiber Mechanical Characterization

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Muscle fibers were attached to hooks with glue made from cellulose nitrate dissolved in acetone. One hook was attached to a dual-mode force/length servo-motor (Aurora Scientific Inc., model 300C) mounted on an X-Y-Z positioner. The other hook was attached to another X-Y-Z positioner that is adjusted to take up the slack in the fiber and then remains fixed during force measurements. Length was controlled and force measured using a National Instruments 16 bit digital/analog controller system controlled by custom software written in Labview (National Instruments Inc.). Sarcomere lengths were measured using laser diffraction with a helium-neon laser with a wavelength of 663nm.
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