Name: evaluation of blood lactate and plasma insulin during high-intensity exercise by antecubital vein catheterization
Uploaded: 2018-05-18T12:30:00.000+00:00
Duration: 4 min 28 s
Description: Watch this Scientific Journal Video about Evaluation of Blood Lactate and Plasma Insulin During High-intensity Exercise by Antecubital Vein Catheterization at JoVE.com

저자는 신문을 읽고에 대 한 박사 P. Karagiannis와 그의 기술 지원에 대 한 교수 T. 호요 인정 하 고 싶습니다.

여기에 설명 된 모든 방법 로컬 윤리 위원회에 의해 승인 되었습니다 (도시샤 대학 윤리 위원회: 15033), 헬싱키의 선언에 의해 설정 된 표준 규격을 따라에서 했다. 동의 모든 참가자 로부터 얻은 것입니다. 참가자 들은 남성 레크리에이션 선수 (20.1 ± 1.2 년, 나이, 체중, 69.7 ± 6.2 k g, 높이, 176.1 ± 5.8 cm; 신체 지방 13.6 ± 1.5% 및 VO2최대 52.6 ± 6.6 mL/min1/kg1).
1입니다. 운동 프로토콜의 설립
참고: 현재 연구는 HIIE 프로토콜 중 antecubital 정 맥에서 혈액 샘플링에 의해 혈액 호르몬 및 대사 산물 역학의 평가의 구성 되어 있습니다.
<ol><li>낮은 강도에서 측에서 자전거의 5 분와 따뜻한을 수행을 요구 하십시오. 워밍업, 후 5 분 동안 휴식 하는 주제를 보자.</li>
	<li>다리 주기 측에서 다음 HIIE를 수행 하기 위해 주제를 물어: 30 s 높은 강도 운동, 구분 하 여 나머지 (그림 1)의 4 분의 3 관찰. 참고: 30 s 복싱 설정 되어야 합니다 강도 평등에서 90%로 이전 수행된 Wingate 테스트의 전원 평균. 다른 곳에 대 한 완전 한 윈 게이트 테스트8 참조.</li>
	<li>30 s 복싱에 대 한 작업 부하를 계산 하려면 다음 수식: 일 = 힘 x 거리 (식 1) 힘 = 질량 x 가속도 (식 2) 일 = (질량 x 가속도) 거리 (식 3) x 참고:이 모델에서는, 질량은 작업 부하 (kg), 그리고 가속도 9.81 m/s2이다. 거리는 바퀴 직경 (1.622 m). 때문에 바퀴 회전 3.7 타임된 /peal 회전, 페달 회전 당 거리 3.7 x 1.662입니다. 또한, 페달 주파수 90 레 브/분1이므로 우리 90 한 페달 거리를 곱하면 해야. 일 = 9.81 x 3.7 x 1.622 x 90 (식 4) x 작업 부하 작업 부하 = 일 / (9.81 x 3.7 x 1.622 x 90) (식 5)</li>
</ol>2입니다. 도관 법
참고: 튜브 및 vacutainers 표시 되어야 합니다 시간 손실을 방지 하려면 미리.
<ol><li>지 혈 대는 도관 법에 대 한 선택 하는 팔을 감싸 줍니다. 이렇게 하려면 선택한 팔 뒷면 신축성 밴드 놓습니다. 스트레칭 밴드, 팔 주위 밴드와 함께 루프를 확인 하 고 탄성을 넥타이.</li>
	<li>보이는 antecubital 정 맥을 선택 하 고 에탄올 또는 알코올 피부를 소독.</li>
	<li>피부와 15 °의 대략적인 각도에서 정 맥으로 멸 균된 정 맥의 끝을 삽입 합니다. 참고:은 정 원심 방향에 인접에서 삽입 한다. Cannulation 성공 하면 혈액의 backflush 관찰 한다.</li>
	<li>손으로 정을 장악 하 고 바늘을 부드럽게 제거 합니다. 참고: 운동을 하는 동안 바늘의 각도 유지, 면 조직 피부와 바늘 사이 사용할 수 있습니다. 테이프와 함께이 구조를 수정 합니다.</li>
	<li>헤 파 린과 첫 번째 혈액 샘플 (약 2.5 mL) aspirate는 vacutainer를 연결 합니다. 직후, 40 분 동안 얼음 상자에 넣어 혈액 샘플을 냉동. 혈액 가스 분석 하려고 하는 경우 보조 도움 요청.</li>
	<li>카 테 터에 튜브를 연결 하 고 혈액 응고를 피하기 위해 튜브의 전체 길이에 헤 파 린 주사. 나비를 닫습니다.</li>
	<li>테이프를 사용 하 여 카 테 터를 고정 시켜야 합니다. 이 시점에서 확인, 피사체의 팔 이동성 혈액 컬렉션에 방해가 되지 않습니다. 이 상태를 확인 하려면 반드시 바늘 위치 어떤 운동에 의해 영향을 받지 않습니다.</li>
</ol>3. 혈액 Samplings
<ol><li>때까지 테에만 피는 vacutainer를 사용 하 여는 헤 파 린을 제거 합니다. 혈액 플래쉬 백을 관찰 하는 경우 2.5 단계에 설명 된 대로 샘플을 수집 합니다.</li>
	<li>샘플 수집 후 혈액 응고를 피하기 위해 카 테 테 르 튜브에 헤 파 린을 다시 삽입할. 이 작업 후 단계 2.5 여러 샘플 컬렉션 반복 수 있습니다.</li>
	<li>마지막 샘플 수집 후 조심 스럽게 cannulation 튜브를 제거 하 고 알코올 피부를 청소. 가능 출혈을 방지 하려면는 catheterization 되었다 장소에 소독된 면 계속 주제 요청.</li>
	<li>혈액 vacutainer 튜브에 수집 후 신중 하 게 1.5 mL 튜브에 혈액의 약 1.5 mL를 통과 하 고 얼음에 튜브를 유지.</li>
	<li>젖 산 검출기를 사용 하 여 나머지 혈액에서 측정 혈액 젖 산. 같은 날에는 플라즈마 혈액 샘플을 (혈액의 약 1.5 mL) 구하십시오.</li>
	<li>플라스마 분리, 혈액 샘플을 4 oC에서 5000 x g에 5 분 동안 원심 및 새로운 1.5 mL 튜브에 상쾌한 분리.</li>
	<li>한 번 더 원심 분리를 반복 하 여 플라즈마 정화.</li>
	<li>혈장 분리 후 호르몬 분석까지-80 oC에서 샘플을 저장 합니다.</li>
	<li>ELISA 키트로 제조업체의 당 ( 재료의 표참조) 프로토콜을 사용 하 여 플라스마 인슐린을 측정 합니다.</li>
</ol>

<ol>
	<li>Wahl, P., Mathes, S., K&#246;hler, K., Achtzehn, S., Bloch, W., Mester, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+active+vs.+passive+recovery+during+Wingate-based+training+on+the+acute+hormonal,+metabolic+and+psychological+response.">Effects of active vs. passive recovery during Wingate-based training on the acute hormonal, metabolic and psychological response.</a> Growth Horm IGF Res. 23 (6), 201-208 (2013).</li><li>Wahl, P., Mathes, S., Achtzehn, S., Bloch, W., Mester, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Active+vs.+passive+recovery+during+high-intensity+training+influences+hormonal+response.">Active vs. passive recovery during high-intensity training influences hormonal response.</a> Int J Sports Med. 35 (7), 583-589 (2014).</li><li>Nalbandian, H. M., Radak, Z., Takeda, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+active+recovery+during+interval+training+on+plasma+catecholamines+and+insulin.">Effects of active recovery during interval training on plasma catecholamines and insulin.</a> J Sports Med Phys Fitness. , (2017).</li><li>Stolen, T., Chamari, K., Castagna, C., Wislff, U. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physiology+of+Soccer.">Physiology of Soccer.</a> Sport Med. 35 (6), 501-536 (2005).</li><li>Bangsbo, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+physiology+of+soccer--with+special+reference+to+intense+intermittent+exercise.">The physiology of soccer--with special reference to intense intermittent exercise.</a> Acta Physiol Scand Suppl. 619, 1-155 (1994).</li><li>MacInnis, M. J., Gibala, M. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Physiological+adaptations+to+interval+training+and+the+role+of+exercise+intensity.">Physiological adaptations to interval training and the role of exercise intensity.</a> J Physiol. 595 (9), 2915-2930 (2017).</li><li>Emberts, T., Porcari, J., Dobers-Tein, S., Steffen, J., Foster, C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Exercise+intensity+and+energy+expenditure+of+a+tabata+workout.">Exercise intensity and energy expenditure of a tabata workout.</a> J Sports Sci Med. 12 (3), 612-613 (2013).</li><li>Smith, J. C., Hill, D. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Contribution+of+energy+systems+during+a+Wingate+power+test.">Contribution of energy systems during a Wingate power test.</a> Br J Sports Med. 25 (4), 196-199 (1991).</li><li>Dotan, R., Bar-Or, O. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Load+optimization+for+the+Wingate+Anaerobic+Test.">Load optimization for the Wingate Anaerobic Test.</a> Eur J Appl Physiol Occup Physiol. 51 (3), 409-417 (1983).</li><li>Carrasco-Benso, M. P., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Human+adipose+tissue+expresses+intrinsic+circadian+rhythm+in+insulin+sensitivity.">Human adipose tissue expresses intrinsic circadian rhythm in insulin sensitivity.</a> FASEB J. 30 (9), 3117-3123 (2016).</li><li>Hatfield, D. L., Nicoll, J. X., Kraemer, W. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Effects+of+Circadian+Rhythm+on+Power,+Force,+and+Hormonal+Response+in+Young+Men.">Effects of Circadian Rhythm on Power, Force, and Hormonal Response in Young Men.</a> J Strength Cond Res. 30 (3), 725-732 (2016).</li></ol>

저자는 공개 없다.

이 연구에서는 antecubital 정 맥 catheterized 했다, 그리고 높은 간격 운동 중 혈액 샘플 수집 성공적으로 되었습니다. 이 방법론의 사용의 예를 들어, 혈액 샘플 플라스마 인슐린에 대 한 혈액 젖 산에 대 한 전후 (플라즈마 분리) 분석 되었다. 이 방법의 주요 장점은 수 혈액 샘플의 컬렉션 짧은 기간입니다. 동시에 그것은 몇 가지 한계는. 예를 들어, 제한 된 운동 양식 수 있는 그것의 사용; 조교 수, 고 ...

신체 활동 중 대사 및 endocrinal 마커의 측정 다른 운동 modalities의 생리 적인 의미를 이해 하는 관련성입니다. 일부 운동 형식 (예: 높은 강도 간격 운동 (HIIE)), 동안 혈액 대사와 호르몬 수준을 상대적으로 짧은 시간1,2,3변동.
구분 하 여 낮은 강렬한 운동 및 수동 기간4,5강도 높은 운동 짧은 기간 (즉, 축구, 농구, 럭비) 많은 스포츠에 의하여 이루어져 있다. HIIE 상기 스포츠와 유사성을 선물 하 고 따라서 선수6을 위한 훈련 방법으로 널리 사용. 또한, 스포츠와의 유사성 때문에 HIIE 사용 되었습니다 모델 운동 생리학7공부 하. 혈액 샘플링은 중요 한 생리 적 변수를 측정 하 고 그것은 자주 연구 목적 및 건강 상태 평가 대 한 사용. 그러나, HIIE 동안 혈액 샘플링 샘플 컬렉션 사이의 짧은 시간 때문에 기술적으로 어려운 수 있습니다. 이 문제에 해결책으로 여기 선물이를 받는 방법을 혈액 샘플 antecubital 정 맥 도관 법에 의해 짧은 기간 동안 과목 수행 HIIE.

<table><tbody><tr><td>Cycle ergometer</td><td>Monark</td><td>MONARK Ergomedic 874 E</td><td></td></tr><tr><td>Catheter</td><td>Terumo</td><td>SR-FF2032</td><td></td></tr><tr><td>Vacutainer</td><td>Terumo</td><td>PZ-D03</td><td></td></tr><tr><td>Tube for catheter</td><td>Terumo</td><td>SP-PTW30L02</td><td></td></tr><tr><td>Heparin</td><td>Terumo</td><td>PF-10HF10UA</td><td></td></tr><tr><td>Insulin ELISA kit</td><td>Abnova</td><td>ELISA Kit KA0921</td><td></td></tr></tbody></table>

evaluation of blood lactate and plasma insulin during high-intensity exercise by antecubital vein catheterization

신체 활동 중 대사 및 endocrinal 마커의 측정 다른 운동 modalities의 생리 적인 의미를 이해 하는 관련성입니다. 일부 동안 형식 (예: 높은 강도 간격 운동) 운동, 혈액 대사와 호르몬 수준을 짧은 기간 변경. 현재 연구에서 우리는 운동 하는 동안 몇 가지 혈액 샘플의 수집 수 있는 antecubital 정 맥 catheterize 하는 방법을 설명 합니다. 인슐린 및 정 맥 젖 산 농도 강도 높은 운동을 하는 동안 설명된 방법의 응용 프로그램에 의해 측정 되었다. 높은 강도 운동 구분 복구의 4 분의 3 30의 복싱 운동에 의하여 이루어져 있다. 마지막 복구 기간 후 윈 게이트 테스트 수행 되었다. Antecubital 정 맥에서 혈액 샘플 전에 각 30 s 한판 승부 후 전에 그리고 Wingate 테스트 후 얻은 했다. 그 결과, 운동을 하는 동안 플라스마 인슐린과 정 맥 혈액 젖 산 변화를 평가 가능 했다.

대표적인 결과로 우리 혈액 젖 산 및 인슐린 유사 6 과목에서 주기 측에 HIIE 동안 측정 하이 프로토콜을 사용. 피크 전력 및 Wingate 테스트에 대 한 평균 전력 732 ± 120와 549 ± 84 와트, 각각 있었다. 평균 전력은 HIIE의 30 s 발작 동안 전원 출력 (494 ± 75 와트)를 계산 하기 위해 사용 되었다.
그림 2 플라즈마 인?...

Watch this Scientific Journal Video about Evaluation of Blood Lactate and Plasma Insulin During High-intensity Exercise by Antecubital Vein Catheterization at JoVE.com

Evaluation of Blood Lactate and Plasma Insulin During High-intensity Exercise by Antecubital Vein Catheterization

여기 우리는 높은 강도 간격 훈련 기간 동안 antecubital 정 맥에서 혈액 샘플을 몇 가지를 얻기 위해 프로토콜을 제시. 이 프로토콜 혈액 대사 산물의 측정에 유용 수 있습니다 하 고 동안 endocrinal 마커 운동.

Antecubital 정 맥 도관 법에 의해 높은 강도 운동 중 혈액 젖 산 염과 플라스마 인슐린의 평가

The measurement of metabolic and endocrinal markers during physical activity is of relevance to understanding the physiological implications of different ...

evaluation-blood-lactate-plasma-insulin-during-high-intensity

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Immunology and Infection

6.4K 조회수.  Kyoto University. 여기 우리는 높은 강도 간격 훈련 기간 동안 antecubital 정 맥에서 혈액 샘플을 몇 가지를 얻기 위해 프로토콜을 제시. 이 프로토콜 혈액 대사 산물의 측정에 유용 수 있습니다 하 고 동안 endocrinal 마커 운동.

비디오: Evaluation of Blood Lactate and Plasma Insulin During High-intensity Exercise by Antecubital Vein Catheterization

Hyperinsulinemic-Euglycemic Clamp in the Conscious Rat

Type 2 diabetes (T2D) is rapidly rising in prevalence. Characterized by either inadequate insulin production or the inability to utilize insulin produced, T2D results in elevated blood glucose levels. The "gold-standard" in assessing insulin sensitivity is a hyperinsulinemic-euglycemic clamp or insulin clamp. In this procedure, insulin is infused at a constant rate resulting in a drop in blood glucose. To maintain blood glucose at a constant level, exogenous glucose (D50) is infused into the venous circulation. The amount of glucose infused to maintain homeostasis is indicative of insulin sensitivity. Here, we show the basic clamp procedure in the chronically catheterized, unrestrained, conscious rat. This model allows blood to be collected with minimal stress to the animal. Following the induction of anesthesia, a midline incision is made and the left common carotid artery and right jugular vein are catheterized. Inserted catheters are flushed with heparinized saline, then exteriorized and secured. Animals are allowed to recover for 4-5 days prior to experiments, with weight gain monitored daily. Only those animals who regain weight to pre-surgery levels are used for experiments. On the day of the experiment, rats are fasted and connected to pumps containing insulin and D50. Baseline glucose is assessed from the arterial line and used a benchmark throughout the experiment (euglycemia). Following this, insulin is infused at a constant rate into the venous circulation. To match the drop in blood glucose, D50 is infused. If the rate of D50 infusion is greater than the rate of uptake, a rise in glucose will occur. Similarly, if the rate is insufficient to match whole body glucose uptake, a drop will occur. Titration of glucose continues until stable glucose readings are achieved. Glucose levels and glucose infusion rates during this stable period are recorded and reported. Results provide an index of whole body insulin sensitivity. The technique can be refined to meet specific experimental requirements. It is further enhanced by the use of radioactive tracers that can determine tissue specific insulin-stimulated glucose uptake as well as whole body glucose turnover.

The hyperinsulinemic-euglycemic clamp is the "gold standard" for the assessment of insulin action. Insulin is infused at a constant rate stimulating glucose uptake. The amount of exogenous glucose infused to counter this drop is indicative of insulin sensitivity. Here the procedure is performed on a conscious, unrestrained rat.

의식 랫에서 인슈린 과다 - Euglycemic 클램프

Type 2 diabetes (T2D) is rapidly rising in prevalence. Characterized by either inadequate insulin production or the inability to utilize insulin produced, ...

연구

의학

Finger-stick Blood Sampling Methodology for the Determination of Exercise-induced Lymphocyte Apoptosis

Exercise is a physiological stimulus capable of inducing apoptosis in immune cells. To date, various limitations have been identified with the measurement of this phenomenon, particularly relating to the amount of time required to isolate and treat a blood sample prior to the assessment of cell death. Because of this, it is difficult to determine whether reported increases in immune cell apoptosis can be contributed to the actual effect of exercise on the system, or are a reflection of the time and processing necessary to eventually obtain this measurement. In this article we demonstrate a rapid and minimally invasive procedure for the analysis of exercise-induced lymphocyte apoptosis. Unlike other techniques, whole blood is added to an antibody panel immediately upon obtaining a sample. Following the incubation period, red blood cells are lysed and samples are ready to be analyzed. The use of a finger-stick sampling procedure reduces the volume of blood required, and minimizes the discomfort to subjects.

Exercise is capable of inducing apoptosis in immune cells. There are various measurement limitations, particularly relating to the amount of time required to isolate and treat a blood sample prior to the assessment. Demonstrated is a rapid and minimally invasive procedure for the analysis of exercise-induced lymphocyte apoptosis.

운동 유발성 Apoptosis 림프구의 결정을위한 손가락 - 스틱 혈액 샘플링 방법론

Exercise is a physiological stimulus capable of inducing apoptosis in immune cells. To date, various limitations have been identified with the measurement ...

면역학 및 감염병학

Hyperinsulinemic-euglycemic Clamps in Conscious, Unrestrained Mice

Type 2 diabetes is characterized by a defect in insulin action. The hyperinsulinemic-euglycemic clamp, or insulin clamp, is widely considered the "gold standard" method for assessing insulin action in vivo. During an insulin clamp, hyperinsulinemia is achieved by a constant insulin infusion. Euglycemia is maintained via a concomitant glucose infusion at a variable rate. This variable glucose infusion rate (GIR) is determined by measuring blood glucose at brief intervals throughout the experiment and adjusting the GIR accordingly. The GIR is indicative of whole-body insulin action, as mice with enhanced insulin action require a greater GIR. The insulin clamp can incorporate administration of isotopic 2[14C]deoxyglucose to assess tissue-specific glucose uptake and [3-3H]glucose to assess the ability of insulin to suppress the rate of endogenous glucose appearance (endoRa), a marker of hepatic glucose production, and to stimulate the rate of whole-body glucose disappearance (Rd).
The miniaturization of the insulin clamp for use in genetic mouse models of metabolic disease has led to significant advances in diabetes research. Methods for performing insulin clamps vary between laboratories. It is important to note that the manner in which an insulin clamp is performed can significantly affect the results obtained. We have published a comprehensive assessment of different approaches to performing insulin clamps in conscious mice1 as well as an evaluation of the metabolic response of four commonly used inbred mouse strains using various clamp techniques2. Here we present a protocol for performing insulin clamps on conscious, unrestrained mice developed by the Vanderbilt Mouse Metabolic Phenotyping Center (MMPC; URL: www.mc.vanderbilt.edu/mmpc). This includes a description of the method for implanting catheters used during the insulin clamp. The protocol employed by the Vanderbilt MMPC utilizes a unique two-catheter system3. One catheter is inserted into the jugular vein for infusions. A second catheter is inserted into the carotid artery, which allows for blood sampling without the need to restrain or handle the mouse. This technique provides a significant advantage to the most common method for obtaining blood samples during insulin clamps which is to sample from the severed tip of the tail. Unlike this latter method, sampling from an arterial catheter is not stressful to the mouse1. We also describe methods for using isotopic tracer infusions to assess tissue-specific insulin action. We also provide guidelines for the appropriate presentation of results obtained from insulin clamps.

The hyperinsulinemic-euglycemic clamp, or insulin clamp, is the gold standard for assessing insulin action in vivo. A method for performing insulin clamps in mice is described. This includes a method for arterial catheterization that permits experiments to be performed in conscious, unrestrained mice with minimal stress.

의식 억제 마우스에 인슈린 과다 - euglycemic 클램프

Type 2 diabetes is characterized by a defect in insulin action. The hyperinsulinemic-euglycemic clamp, or insulin clamp, is widely considered the "gold ...

Determining the Contribution of the Energy Systems During Exercise

One of the most important aspects of the metabolic demand is the relative contribution of the energy systems to the total energy required for a given physical activity. Although some sports are relatively easy to be reproduced in a laboratory (e.g., running and cycling), a number of sports are much more difficult to be reproduced and studied in controlled situations. This method presents how to assess the differential contribution of the energy systems in sports that are difficult to mimic in controlled laboratory conditions. The concepts shown here can be adapted to virtually any sport.
The following physiologic variables will be needed: rest oxygen consumption, exercise oxygen consumption, post-exercise oxygen consumption, rest plasma lactate concentration and post-exercise plasma peak lactate. To calculate the contribution of the aerobic metabolism, you will need the oxygen consumption at rest and during the exercise. By using the trapezoidal method, calculate the area under the curve of oxygen consumption during exercise, subtracting the area corresponding to the rest oxygen consumption. To calculate the contribution of the alactic anaerobic metabolism, the post-exercise oxygen consumption curve has to be adjusted to a mono or a bi-exponential model (chosen by the one that best fits). Then, use the terms of the fitted equation to calculate anaerobic alactic metabolism, as follows: ATP-CP metabolism = A1 (mL . s-1) x t1 (s). Finally, to calculate the contribution of the lactic anaerobic system, multiply peak plasma lactate by 3 and by the athlete&#x2019;s body mass (the result in mL is then converted to L and into kJ).
The method can be used for both continuous and intermittent exercise. This is a very interesting approach as it can be adapted to exercises and sports that are difficult to be mimicked in controlled environments. Also, this is the only available method capable of distinguishing the contribution of three different energy systems. Thus, the method allows the study of sports with great similarity to real situations, providing desirable ecological validity to the study.

This protocol allows researchers focused on exercise and sports sciences to determine the relative contribution of three different energy systems to the total energy expenditure during a large variety of exercises.

운동하는 동안 에너지 시스템의 공헌을 결정

One of the most important aspects of the metabolic demand is the relative contribution of the energy systems to the total energy required for a given ...

생물학

Combined Intravital Microscopy and Contrast-enhanced Ultrasonography of the Mouse Hindlimb to Study Insulin-induced Vasodilation and Muscle Perfusion

It has been demonstrated that insulin's vascular actions contribute to regulation of insulin sensitivity. Insulin's effects on muscle perfusion regulate postprandial delivery of nutrients and hormones to insulin-sensitive tissues. We here describe a technique for combining intravital microscopy (IVM) and contrast-enhanced ultrasonography (CEUS) of the adductor compartment of the mouse hindlimb to simultaneously visualize muscle resistance arteries and perfusion of the microcirculation in vivo. Simultaneously assessing insulin's effect at multiple levels of the vascular tree is important to study relationships between insulin's multiple vasoactive effects and muscle perfusion. Experiments in this study were performed in mice. First, the tail vein cannula is inserted for the infusion of anesthesia, vasoactive compounds and ultrasound contrast agent (lipid-encapsulated microbubbles). Second, a small incision is made in the groin area to expose the arterial tree of the adductor muscle compartment. The ultrasound probe is then positioned at the contralateral upper hindlimb to view the muscles in cross-section. To assess baseline parameters, the arterial diameter is assessed and microbubbles are subsequently infused at a constant rate to estimate muscle blood flow and microvascular blood volume (MBV). When applied before and during a hyperinsulinemic-euglycemic clamp, combined IVM and CEUS allow assessment of insulin-induced changes of arterial diameter, microvascular muscle perfusion and whole-body insulin sensitivity. Moreover, the temporal relationship between responses of the microcirculation and the resistance arteries to insulin can be quantified. It is also possible to follow-up the mice longitudinally in time, making it a valuable tool to study changes in vascular and whole-body insulin sensitivity.

Insulin-induced vasodilation regulates muscle perfusion and increases the microvascular surface area (microvascular recruitment) available for solute exchange between blood and tissue interstitium. Combined intravital microscopy and contrast-enhanced ultrasonography is presented to simultaneously assess insulin&#39;s action at the larger vessels and the microcirculation in vivo.

Intravital 현미경 검사 법 및 대비 향상 된 초음파 마우스 Hindlimb의 인슐린 유도 된 혈관과 근육 관류 결합

It has been demonstrated that insulin's vascular actions contribute to regulation of insulin sensitivity. Insulin's effects on muscle perfusion regulate ...

Experimental Protocol of a Three-minute, All-out Arm Crank Exercise Test in Spinal-cord Injured and Able-bodied Individuals

Reliable exercise protocols are required to test changes in exercise performance in elite athletes. Performance improvements in these athletes may be small; therefore, sensitive tools are fundamental to exercise physiology. There are currently many exercise tests that allow for the examination of exercise capacity in able-bodied athletes, with protocols mainly for lower-body or whole-body exercise. There is a trend to test athletes in a sport-specific setting that closely resembles the actions that the participants are used to performing. Only a few protocols test short-term, high-intensity exercise capacity in participants with an impairment of the lower body. Most of these protocols are very sport-specific and are not applicable to a wide range of athletes. One well-known test protocol is the 30 s Wingate test, which is well-established in cycling and in arm crank exercise testing. This test analyzes high-intensity exercise performance over a 30 s time duration. In order to monitor exercise performance over a longer duration, a different method was modified for application to the upper body. The 3 min, all-out arm crank ergometer test allows athletes to be tested in a manner specific to 1,500 m wheelchair racing (in terms of exercise duration), as well as to upper body exercises such as rowing or hand-cycling. In order to increase the reliability with identical test conditions, it is crucial to precisely replicate settings such as the resistance (i.e., torque factor) and the position of the participants (i.e., the height of the crank, the distance between the crank and the participant, and the fixation of the participant). Another important issue concerns the beginning of the exercise test. Fixed revolutions per minute are required to standardize the test conditions for the start of the exercise test. This exercise protocol shows the importance of accurate operations to reproduce identical test conditions and settings.

We present a protocol to test the aerobic and anaerobic power of the upper body muscles over a duration of 3 min in able-bodied as well as in paraplegic and tetraplegic individuals. The protocol presents specific modifications in its application for upper-body exercise in individuals with or without disability.

척수 손상 및 에이블 바디의 3 분간 전면 팔 크랭크 운동 테스트의 실험 프로토콜

Reliable exercise protocols are required to test changes in exercise performance in elite athletes. Performance improvements in these athletes may be ...

Postconditioning with Lactate-enriched Blood for Cardioprotection in ST-segment Elevation Myocardial Infarction

The beneficial effects of reperfusion therapy for ST-segment elevation myocardial infarction (STEMI) is attenuated by reperfusion injury. No approach has been proven successful in preventing this injury in the clinical setting to date. Meanwhile, a novel approach for cardioprotection in patients with STEMI, i.e., postconditioning with lactate-enriched blood (PCLeB), has recently been reported. PCLeB is a modification of the original protocol of postconditioning, aimed at increasing the delay in the recovery from tissue acidosis produced during ischemia. This was sought to achieve controlled reperfusion with tissue oxygenation and minimal lactate washout. In this modified postconditioning protocol, the duration of each brief reperfusion is gradually increased in a stepwise manner from 10 to 60 s. Each brief ischemic period lasts for 60 s. At the end of each brief reperfusion, injection of lactated Ringer&#39;s solution (20&#8211;30 mL) is performed directly into the culprit coronary artery immediately before the balloon inflation and the balloon is quickly inflated at the lesion site, so that the lactate is trapped inside the ischemic myocardium during each brief repetitive ischemic period. After seven cycles of balloon inflation and deflation, full reperfusion is performed. Stenting is performed thereafter, and the percutaneous coronary intervention is completed. Excellent in-hospital and 6 month outcomes in a limited number of patients with STEMI treated using PCLeB have already been reported. This method article provides a detailed description of each step of the PCLeB procedures.

Herein, we present a protocol for postconditioning with lactate-enriched blood, which is a novel approach for cardioprotection. This protocol comprises&#160;intermittent reperfusion and timely coronary injections of lactated Ringer&#39;s solution. This can be applied to ST-segment elevation myocardial infarction patients who undergo primary percutaneous coronary intervention.

ST 세그먼트 고도 심근 경색에서 심장 보호를 위한 젖산 농축 혈액으로 후컨디셔닝

The beneficial effects of reperfusion therapy for ST-segment elevation myocardial infarction (STEMI) is attenuated by reperfusion injury. No approach has ...

Measurement of Myocardial Lactate Production for Diagnosis of Coronary Microvascular Spasm

In about a quarter of patients with angina and non-obstructive coronary arteries, no epicardial spasm is noted on coronary arteriography during an angina attack. Since the pressure-rate product is almost identical at rest and the onset of attack in those patients, the decrease in coronary blood flow rather than increased myocardial oxygen consumption is likely to explain myocardial ischemia, indicating a substantial involvement with coronary microvascular spasm (MVS). Myocardial lactate production, which could be defined as a negative myocardial lactate extraction ratio (ratio of the coronary arterial-venous difference in lactate concentration to arterial concentration), is considered indicative of objective evidence to support the emerging myocardial ischemia. Thus, monitoring of the myocardial lactate production and the emergence of chest pain and ischemic electrocardiographic changes during acetylcholine (ACh) provocation testing is of significant value for detecting the entity of MVS. Practically, 1 min after incremental doses of ACh (20, 50, and 100 &#956;g) are administered into the left coronary artery (LCA), paired samples of 1 mL of blood are collected from the LCA ostium and coronary sinus for measurement of lactate concentration by a calibrated automatic lactate analyzer. Then, the development of MVS could be confirmed by negative myocardial lactate extraction ratio despite the absence of angiographically demonstrable epicardial coronary spasm or before its occurrence throughout ACh provocation testing. In conclusion, assessment of myocardial lactate production is essential and valuable for the diagnosis of MVS.

Myocardial lactate production (coronary arterial-venous difference in serum lactate level) during coronary spasm provocation testing is considered as a highly sensitive marker that reflects acetylcholine-induced myocardial ischemia due to microvascular spasm. This article presents the procedures to assess myocardial lactate production for the diagnosis of coronary microvascular spasm.

관상동맥 미세혈관 경련 진단을 위한 심근 젖산 생산 측정

In about a quarter of patients with angina and non-obstructive coronary arteries, no epicardial spasm is noted on coronary arteriography during an angina ...

Using a Combination of Indirect Calorimetry, Infrared Thermography, and Blood Glucose Levels to Measure Brown Adipose Tissue Thermogenesis in Humans

In mammals, brown adipose tissue (BAT) is activated rapidly in response to cold in order to maintain body temperature. Although BAT has been studied greatly in small animals, it is difficult to measure the activity of BAT in humans. Therefore, little is known about the heat-generating capacity and physiological significance of BAT in humans, including the degree to which components of the diet can activate BAT. This is due to the limitations in the currently most used method to assess the activation of BAT-radiolabeled glucose (fluorodeoxyglucose or 18FDG) measured by positron emission tomography-computerized tomography (PET-CT).
This method is usually performed in fasted subjects, as feeding induces glucose uptake by the muscles, which can mask the glucose uptake into the BAT. This paper describes a detailed protocol for quantifying total-body human energy expenditure and substrate utilization from BAT thermogenesis by combining indirect calorimetry, infrared thermography, and blood glucose monitoring in carbohydrate-loaded adult males. To characterize the physiological significance of BAT, measures of the impact of BAT activity on human health are critical. We demonstrate a protocol to achieve this by combining carbohydrate loading and indirect calorimetry with measurements of supraclavicular changes in temperature. This novel approach will help to understand the physiology and pharmacology of BAT thermogenesis in humans.

Here, we present a protocol to quantify the physiological significance of the impact of brown adipose tissue (BAT) activity on human metabolism. This is achieved by combining carbohydrate loading and indirect calorimetry with measurements of supraclavicular changes in temperature. This novel approach can help develop a pharmacological target for BAT thermogenesis in humans.

간접 열량계, 적외선 체온 측정 및 혈당 수치의 조합을 사용하여 인간의 갈색 지방 조직 열 발생을 측정합니다.

In mammals, brown adipose tissue (BAT) is activated rapidly in response to cold in order to maintain body temperature. Although BAT has been studied ...

근력 운동량과 비만에서 인슐린 감수성에 미치는 영향 평가

Randomized Controlled Trial to Study the Acute Effects of Strength Exercise on Insulin Sensitivity in Obese Adults

An acute session of strength exercise (SE) ameliorates insulin sensitivity (IS) for several hours; however, the effects of SE volume (i.e., number of sets) have not been studied thoroughly. Although it is intuitive that some SE is better than none, and more is better than some for the improvement of IS, high-volume sessions might be challenging for diseased populations to complete, especially obese adults, for whom even a brisk walk can be challenging. This protocol details a randomized clinical trial to assess the acute effects of SE on IS in obese adults. The inclusion criteria are body mass index &#62;30 kg/m2, central obesity (waist circumference &#62;88 cm and &#62;102 cm for women and men, respectively), and age &#62;40 years. Participants will be familiarized with the SE (7 exercises targeting major muscle groups) and then will perform three sessions in a randomized order: session 1 - high-volume session (3 sets/exercise); session 2 - low-volume session (1 set/exercise); session 3 - control session (no exercise). Diet will be controlled the day before and on the day of the sessions. Sessions will be completed at night, and an oral glucose tolerance test will be performed the next morning, from which several indexes of IS will be derived, such as the area under the curve (AUC) of glucose and insulin, the Matsuda index, the Cederholm index, the muscle IS index, and the Gutt index. Based on pilot studies, we expect ~15% improvement in IS (insulin AUC, and Matsuda and Cederholm indexes) after the high-volume session, and ~8% improvement after the low-volume session compared to the control session. This study will benefit individuals who find high-volume SE sessions challenging but still aim to improve their IS by investing 1/3 of their time and effort.

저자 스포트라이트: 저항력 운동량 감소가 신진대사 건강에 미치는 영향 탐구 

This study describes a randomized controlled trial protocol aiming at assessing the acute effects of strength exercise volume on insulin sensitivity in obese individuals.

비만 성인의 인슐린 감수성에 대한 근력 운동의 급성 효과를 연구하기 위한 무작위 대조 시험

An acute session of strength exercise (SE) ameliorates insulin sensitivity (IS) for several hours; however, the effects of SE volume (i.e., number of ...