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Accusport

Manufactured by Roche
Sourced in Germany, Switzerland

The Accusport is a laboratory instrument designed for the analysis and determination of various analytes. It utilizes electrochemical detection techniques to provide accurate and reliable measurements. The core function of the Accusport is to quantify the levels of specific substances in samples, enabling researchers and clinicians to obtain valuable data for their scientific and medical applications.

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8 protocols using accusport

1

Incremental Bench Step Test for Lactate Threshold

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The subjects performed an incremental step bench test to volitional exhaustion to determine their lactate threshold and the onset of blood lactate accumulation (OBLA). The initial load was set at 15 W. Each stage lasted 5 minutes and was increased by 15 W per stage until the subject could no longer continue. To calculate the power of the bench step, the following procedures were adopted: determination of body mass, step height and frequency increases [Power = strength (N) × speed (m/s)]. Thus, the speed was adjusted individually in each stage to generate the necessary intensity (15 W).
Prior to the first stage and at the end of each stage, LA concentration was determined with a portable lactate analyzer (Accusport, Roche, Brazil). The lactate threshold was considered the last period in which the LA concentration did not differ by more than 1 mmol·l−1 from the rest value. The OBLA was calculated assuming a fixed concentration of 4 mmol·l−1 (Svedahl and McIntosh, 2003 (link)). The test was terminated when two consecutive LA measurements were higher than 4 mmol·l−1.
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2

Submaximal Exercise Test for Horses

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A standardized submaximal exercise test (SET) was performed by each horse on the treadmill at the beginning of the study to determine the blood lactate running speed relationship (BLRS). Blood samples were drawn from the jugular vein prior to SET, but after warm-up. Warm-up consisted of 5 min at 1.7 m/s and 5 min at 4.0 m/s on a 0% slope.
The SET on the treadmill inclined at 6% consisted of 5 min at each speed, starting at 4.0 m/s with subsequent steps increasing incrementally by 0.5 m/s. Between each step, the treadmill was stopped for 60 s, blood samples were drawn (within 15 s) by puncture of the jugular vein into Li-heparinized evacuated tubes (Becton Dickinson, Heidelberg, Germany) and blood Lactate (LA) was determined immediately (Accusport™; Roche Diagnostics, Mannheim, Germany). When the horse reached a speed at which the blood LA concentration was at or above 4 mmol/L, the SET ended. A BLRS curve was generated using exponential regression analysis and used to calculate the horse’s speed at which the LA concentration reached 4 mmol/L (v4) [22 ].
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3

Blood Lactate Dynamics during Exercise

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Blood samples were collected at rest, in the morning, before feeding (measurement 0; LAC 0), immediately after (1–3 min; measurement 1; LAC 1), and 30 min after exercise (measurement 2; LAC 2). All samplings were a part of standard veterinary diagnostic procedures according to Polish legal regulations (art 1.2 (5) Ust. z dnia 15 stycznia 2015 r. o ochronie zwierzat wykorzystywanych do celów naukowych lub edukacyjnych, Dz.U.2018.0.1207 (Resolution on the animals protection used for scientific and educational purposes); the European directive EU/2010/63 approval of the Local Commission for Ethics in Animal Experiments was not required. Blood samples were acquired by a jugular venipuncture using BD Vacutainer® dry tubes (Plymouth, UK). Blood lactate concentrations were determined immediately after blood collection using an Accusport® (Roche Diagnostics, Basel, Switzerland) (LAC, mmol/L).
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4

Equine Hematology and Blood Biochemistry

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EDTA blood samples were kept at +4 °C and examined within 5 h in an automated analyzer calibrated for equine species (ABC Vet, Horiba ABX). The following hematological parameters were taken into account: white blood cell count (WBC, × 109/L), red blood cell count (RBC, × 1012/L), hemoglobin concentration (HGB, mmol/L), hematocrit (HCT, %), mean corpuscular volume (MCV, fL), mean corpuscular hemoglobin (MCH, gL), mean corpuscular hemoglobin concentration (MCHC, mmol/L), and red cell distribution width (RDW, %).
Blood lactate concentrations (LAC, mmol/L) were determined in whole blood immediately after blood collection using an Accusport® (Roche Diagnostics, Basel, Switzerland). The dry tubes were centrifuged (2000 ×
g, 5 min) and serum-free from any apparent hemolysis was aspirated for further analyses. Total serum protein (TSP, g/L) concentration was measured by the refractometer technique (Reichert Rhino Vet 360, Munich, Germany). Creatine phosphokinase (CPK, U/L) and aspartate aminotransferase (AST, U/L) activities were determined using an automated clinical biochemistry analyzer (Miura One, ISE. S.r.l., Albuccione, Italy). For all measurements, Pointe Scientific (5449 Research Dr, Canton, MI 48188, USA) reagents, standards, calibrators, and controls were used.
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5

Blood Lactate Measurement Protocol

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Blood lactate was collected before and after the workout. The blood sample was collected by a puncture in the distal phalanx of the index finger of the participants in aseptic conditions using a lancet (Roche®, Accu-Chek Safe-T-Pro Uno, USA) and disposable gloves (Cremer®, Brazil). After discarding the first drop of blood, 25 μL of capillary blood was collected. For the determination of blood lactate, a portable lactate analyzer (Roche®, Accusport, USA) duly validated 24 was used. Before testing, the lactate analyzer was calibrated with different standard solutions of known lactate concentrations (2, 4, 8, and 10 mmol•L -1 ).
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6

Blood Lactate Responses to Simulated Fights

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Blood lactate responses (LA) of each participant were evaluated at Pre (before the fight and warm-up), and 1 and 15 min Post simulated fights. Lactate concentration was obtained using a portable lactate analyzer (Accusport; Boehringer Mannheim, Germany) (Bishop, 2001 (link); Pyne et al., 2000 (link)).
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7

Capillary Blood Lactate Measurement

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For lactate measurements, capillary blood was obtained from earlobe and assessed with reagent strips (BM-Lactate, Roche Diagnostics, Germany) [27 (link)] and a portable handheld lactate meter (Accusport®, Boehringer Mannheim, Germany).
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8

Measuring Capillary Lactate Levels

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For measuring capillary lactate concentrations, blood samples from the fingertip 5 were obtained at rest before the 400 m run tests, immediately after finishing them 6 and four times during the recoveries: at min 10, 20, 30 and 40. These samples 7 were analyzed immediately after they were drawn using the Accusport portable 8 blood lactate analyzer (Boehringer Mannheim, Manheim, Germany), which has 9 been found to be valid and reliable (Bishop 2001; Pinnington and Dawson 2001). 10 Furthermore, only one device was used for all the measurements in order to avoid 11 potential error due to the use of different analyzers (Bishop 2001; Pinnington and 12
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