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Tb 611t

Manufactured by Nihon Kohden
Sourced in Japan

The TB-611T is a blood pressure monitor designed for use in a clinical setting. It is capable of automatically measuring and recording blood pressure and pulse rate data.

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7 protocols using tb 611t

1

Measuring Isometric Contraction of Coronary Artery Smooth Muscle

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Isometric contractions of the coronary artery smooth muscle strips without the endothelium and adventitia were measured using a force transducer (TB-611T; Nihon Kohden, Tokyo, Japan), as previously described.17 The experimental process is briefly summarized as follows. These strips were mounted vertically in an organ bath filled with Krebs solution, gassed with 5% CO2/95% O2, and maintained at 37°C in a force transducer. After the relaxed smooth muscle tissue strips were stable in the solution for 15 minutes, we stimulated smooth muscle strips with 118 mM K+ for 5 minutes. Next, 118 mM K+ solution was washed out with Krebs solution. After 5 minutes, we applied resting tension. After 5 minutes of continuous resting tension, 118 mM K+ was used to induce depolarization contraction of smooth muscle strips for an additional 5 minutes. Next, the above cycle process was repeated until the depolarization-induced contraction caused by 118 mM K+ reached a maximum, that is, the resting tension was optimized. After the resting tension was optimized, the effects of posttreatment and pretreatment hesperetin on the maximum and steady-state forces of contractions induced by 30 μM SPC or 40 mM K+ were examined. The extent of contraction inhibition by hesperetin is described as the percentage by which the contraction induced by 30 μM SPC or 40 mM K+ was inhibited.
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2

Rat Uterine Contractility Assay

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Myometrial strips were prepared from the dissected rat uterus, as described previously [51 (link),52 (link)]. Each strip (width: 2 to 3 mm, length: 10–15 mm) was attached to a holder under 1 g of resting tension, equilibrated for 30 min in PSS, and then repeatedly treated with a 72.7-mM KCl solution (high-KCl) until the response stabilized. PSS contained 136.9-mM NaCl, 5.4-mM KCl, 1.5-mM CaCl2, 1.0-mM MgCl2, 23.8-mM NaHCO3, 5.5-mM glucose, and 0.01-mM ethylenediaminetetraacetic acid. A solution with high KCl concentration was prepared by replacing NaCl with an equimolar quantity of KCl. Calcium-free PSS was prepared without CaCl2. These solutions were saturated with a 95% O2/5% CO2 mixture at 37 °C (pH 7.4). After pretreatment with high KCl, a steroid hormone or a vehicle (DMSO) was added, and the myometrial contractile activity was recorded isometrically using a force-displacement transducer (TB611T; Nihon Kohden, Tokyo, Japan) connected to a Model 3134 strain amplifier. Uterine strips in each experiment were prepared from the uterine tissue of one animal (one strip/one group), and the experiment was repeated six times on each individual rat. Data were analyzed using the Unique Acquisition software package (Microsoft Windows 7; Unique Medical, Tokyo, Japan).
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3

Isometric Force Measurement of Pulmonary Vein

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The isometric contractile force of isolated tissue preparations was recorded. One end of the pulmonary vein preparation was pinned down on a silicon block at the bottom of the organ bath and the other end was attached to a needle connected to a force-displacement transducer (TB-611T, Nihon Kohden, Tokyo, Japan). The detected contractile force was amplified with a carrier amplifier (AP-621G, Nihon Kohden, Tokyo) and digitized by an A/D converting interface (Power Lab, AD Instruments, Dunedin, New Zealand).
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4

Neonatal Mouse Ventricular Contractility

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Whole ventricles were rapidly isolated from neonatal (0 to 2 days) ddY strain mice. Preparations were placed horizontally in a 20 mL organ bath containing the modified Ringer solution of the following composition (mM): NaCl 118.4, KCl 4.7, CaCl2 2.5, MgSO4 1.2, NaHCO3 24.9, KH2PO4 1.2, glucose 11.0 (pH 7.4 at 36 °C). The solution was gassed with 95% O2- 5% CO2 and maintained at 36 ± 0.5 °C. The preparations were driven by rectangular current pulses (1 Hz, 3 ms, 1.5 × threshold voltage) through a pair of platinum plate electrodes (field stimulation) generated from an electronic stimulator (SEN-3301; Nihon Kohden, Tokyo, Japan). The contractile force was recorded isometrically with a force-displacement transducer (TB-611T; Nihon Kohden) connected to a carrier amplifier (AP-621G; Nihon Kohden). The output was digitized by an A/D converting interface (Power Lab/4SP, AD Instruments, Chalgrove, UK) and analyzed by Chart 7 software (AD Instruments). The resting tension on each preparation was applied so that the muscle was stretched to the peak of its length/tension curve. The contractile force in the presence of phenylephrine was measured at 15 min after the addition of phenylephrine when it had reached a steady state. In all the experiments, experimental solutions contained propranolol (1 µM) to eliminate the β-adrenergic effects of phenylephrine.
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5

Measuring Muscle Contractile Properties

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To eliminate potential influences of acute muscle contractions on subsequent analyses, EDL and TA muscles were used for force measurements and biochemical analyses, respectively. Isolated EDL muscles were mounted between two platinum plate stimulation electrodes (Iwashiya Kishimoto Medical Instruments, Kyoto, Japan) and connected to an isometric force transducer (TB-611 T; Nihon Kohden). The muscles were placed in Krebs-Ringer solution [in mM: 115 NaCl, 20 NaHCO 3 , 11 glucose, 5 KHCO 3 , 5 N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid, 2 CaCl 2 , 1 MgCl 2 , 0.4 glutamine, and 0.3 glutamic acid] with continuous bubbling of 95% O 2 -5% CO 2 , maintaining an extramuscular pH of 7.4. Isometric contractions were elicited via direct stimulation at 10 and 80 Hz with supramaximal voltage, 1/ms pulses, and 1/s trains. Force output was recorded on a personal computer and analyzed using Lab-Chart version 8 (ADInstruments, CO, USA). All measurements were performed in a temperature-controlled room at 25 °C. Absolute force was normalized to cross-sectional area, calculated as wet muscle weight divided by the product of muscle length and density (1.06 mg/mm 3 ).
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6

Muscle Tension Measurement with Hypoxia

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The longitudinal muscle layer was stripped from the ileum circular muscle as described by Paton and Aboo Zar [24 (link)]. The
thoracic aorta was cut into spiral strips, and the endothelium was removed by gentle rubbing with absorbent cotton. The longitudinal muscle, which was divided
into strips approximately 5–6 mm in width and 15 mm in length, and the thoracic aorta and renal artery strips of approximately 2–3 mm in width and 8–10 mm in
length, two strips of iris sphincter muscles were cut from each eye (with the ciliary margin removed), were incubated with PSS containing (in mM) 136.8 NaCl,
5.4 KCl, 2.5 CaCl2, 1.0 MgCl2, 11.9 NaHCO3 and 5.5 glucose. The PSS was aerated with 95% O2 and 5% CO2 to
adjust to pH 7.2 and maintained at 37°C. For inducing hypoxia, PSS was aerated with 95% N2 instead of O2.
Muscle tension was isometrically recorded. One end of each strip was bound to a glass holder, and the other end was connected by a silk thread to a strain
gauge transducer (TB-611T; Nihon Kohden, Tokyo, Japan) in an organ bath containing PSS with a resting tension of 0.5 g. The muscle strips were equilibrated for
30 min to obtain stable contractility induced by hyperosmotic 65 mM KCl (H-65K+).
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7

Porcine Stomach Muscle Tension Assay

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The stomachs from adult pigs of either sex were obtained from a local abattoir. The mucosal layer was removed by cutting with fine scissors, and strips of circular and longitudinal smooth
muscle were isolated from the fundus region. Muscle strips (approximately 2 mm in width and 7–8 mm in length) were incubated in physiological salt solution (PSS) containing (in mM) 136.8
NaCl, 5.4 KCl, 11.9 NaHCO3, and 5.6 glucose. PSS was aerated with 95% O2 and 5% CO2 to adjust the pH to 7.2 at 37°C. In hypoxic conditions, PSS was aerated
with 95% N2 and 5% CO2 instead of 95% O2 and 5% CO2, and pH did not change even in hypoxic condition.
Muscle tension was recorded isometrically. One end of each strip was bound to a glass holder and the other end was connected by a silk thread to a strain-gauge transducer (TB-611T; Nihon
Kohden, Tokyo, Japan) in an organ bath containing PSS with a resting tension of 2.0 g. Muscle strips were equilibrated for 30 min to obtain stable contractility induced by hyperosmotic 65 mM
KCl (H-65K+). The developed tension was expressed as a percentage by assuming the values at rest in PSS to be 0% and those at 15 min after addition of H-65K+ or 0.3
µM CCh to be 100%. In the present study, we tentatively expressed decrease in muscle contraction as relaxation.
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