A densidade como uma nova métrica da quantificação de cargas no treinamento de força / Density as a new metric to quantify strength training loads

O objetivo do estudo foi realizar um breve comunicado sobre a adoção da densidade com uma nova métrica de quantificação de cargas no treinamento de força. Descrevemos como quantificá-la e destacamos as possíveis implicações da sua manipulação. Uma vez que considera o intervalo de recuperação entre as séries - onde podem ocorrer processos metabólicos importantes, como a ressíntese de fosfocreatina - a densidade pode ser um parâmetro representativo da magnitude do estresse metabólico induzido pelas sessões. Recomendamos que treinadores e pesquisadores da área de ciências do esporte passem a reportar quantificar e reportar a densidade dos treinos. Técnicas de treinamento que manipulam as pausas entre as séries, repetições e exercícios, como os treinos em circuito, o restpause, cluster training, intra-set rest e/ou inter-repetion rest, podem ter novas análises e, consequentemente, resultados interessantes a serem reportados.(AU)

The aim of the study was to provide a short communication about the adoption of density as a new metric to quantify strength training loads. We describe how quantify and highlighted the possible implications of density manipulation. Since considers the rest interval between sets - where important metabolic process such as phosphocreatine resynthesizes may occurs ­ density may represent the magnitude of metabolic stress induced by training session. In this sense, is recommended that sports sciences coach's and researchers report the training density. Training techniques that manipulate the rest intervals between sets, repetitions, and exercises, such as circuit tra ining, rest pause, cluster training, intra-set rest, and/or inter-repetition rest may have new analysis, and consequently interesting results to be reported.(AU)

Role of the phosphocreatine system on energetic homeostasis in skeletal and cardiac muscles / Papel do sistema da fosfocreatina na homeostase energética das musculaturas esquelética e cardíaca

Adenosine triphosphate is the present energy currency in the body, and is used in various cellular and indispensable processes for the maintenance of cell homeostasis. The regeneration mechanisms of adenosine triphosphate, from the product of its hydrolysis – adenosine diphosphate – are therefore necessary. Phosphocreatine is known as its quickest form of regeneration, by means of the enzyme creatine kinase. Thus, the primary function of this system is to act as a temporal energy buffer. Nevertheless, over the years, several other functions were attributed to phosphocreatine. This occurs as various isoforms of creatine kinase isoforms have been identified with a distinct subcellular location and functionally coupled with the sites that generate and use energy, in the mitochondria and cytosol, respectively. The present study discussed the central and complex role that the phosphocreatine system performs in energy homeostasis in muscle cells, as well as its alterations in pathological conditions.

A adenosina trifosfato é a moeda corrente de energia no organismo, sendo utilizada em diversos processos celulares e indispensável para a manutenção da homeostase celular. Mecanismos de regeneração da adenosina trifosfato, a partir de seu produto de hidrólise – a adenosina difosfato – são, dessa forma, necessários. A fosfocreatina é conhecidamente sua fonte mais rápida de regeneração, por meio da enzima creatina quinase. Assim, a principal função desse sistema é atuar como um tampão temporal de energia. Entretanto, ao longo dos anos, diversas outras funções foram atribuídas à fosfocreatina. Isso ocorreu à medida que foram identificadas diversas isoformas da creatina quinase com localização subcelular distinta e acopladas de forma funcional aos sítios geradores e utilizadores de energia, na mitocôndria e citosol, respectivamente. O presente trabalho discutiu o papel central e complexo que o sistema da fosfocreatina desempenha na homeostase energética nas células musculares, bem como suas alterações em quadros patológicos.

Non-invasive assessment of oxidative capacity in young Indian men and women: a 31P magnetic resonance spectroscopy study.

It is generally assumed that men display greater strength and muscle capacity than women. However, previous biochemical and histological studies have shown that men have greater capacity for anaerobic metabolism and women have higher or similar oxidative metabolism. Therefore, in the present study, we estimated oxidative capacity of gastrocnemius muscle and compared in Indian men and women using non-invasive in vivo 31P magnetic resonance spectroscopy (MRS). Healthy subjects (8 young males and 9 females, age-matched) performed plantar flexion exercise within a magnet and MRS measurements of inorganic phosphate (Pi), phosphocreatine (PCr), ADP, and pH of the calf muscles were carried out using a 1.5 T whole-body MRI system. PCr values during recovery were fitted to an exponential curve, and oxidative capacity was calculated using rate constant (k(PCr)), as an index of oxidative phosphorylation. When men and women were compared for different metabolic ratios, ADP, pH, k(PCr) and oxidative capacity, all parameters turned out to be statistically insignificant. The results showed no gender effect on skeletal muscle oxidative metabolism. The study demonstrated the usefulness of such non-invasive method to indirectly measure the oxidative capacity of the muscle based on PCr recovery.

Parâmetros mecânicos e metabólicos do desempenho em intensidade supra-máxima de nado crawl / Mechanical and metabolic parameters of front crawl swim performance at supramaximal intensity

O objetivo deste estudo foi analisar o desempenho supra-máximo no nado crawl (vmax) pelas relações entre energia anaeróbia (Eanaer), potência muscular (Po) e propulsiva (Pu), eficiência mecânica (emec) e propulsiva (ep), economia e força de arrasto (Fr). Onze competidores submeteram-se à avaliação de Fr pelo método de Perturbação da Velocidade e à estimativa da ep, pelas relações entre Fr e a ação do hidrofólio. Eanaer foi quantificada pelo equivalente energético do lactato e da fosfocreatina. Correlações de vmax com Eanaer (0,71), economia (0,65), Fr (0,68), Pu (0,79) e Po (0,69) sugerem que força, potência e disponibilidade de energia sustentam o desempenho em vmax. Contudo, ao restringir Eanaer em vmax, apenas a economia acomoda-se a esta condição (-0,95), enquanto que emec torna-se determinante para Fr (0,97), Pu (0,90) e Po (0,98). Conclui-se que a taxa de trabalho é decisiva no desempenho supramáximo, e que Eanaer subsidia sua produção, mas quando restrita, emec e economia interagem-se como fatores fundamentais para manter a taxa de trabalho no patamar demandado por esta condição de nado.

The purpose of this study was to analyze crawl performance at supramaximal intensity (vmax) from relationships between anaerobic energy (Eanaer), mechanical and propulsive power (Po, Pu), mechanical and propulsive efficiency (emec, ep), and drag force (Fr). Eleven experience swimmers were undergone to the measurement of Fr from the method of Velocity Perturbation, and to estimative the ep from Fr relationships to hydrofoil action. Eanaer was estimated from lactate and phosphocreatine energy equivalents. Correlations of vmax to Eanaer (0,72), economy (0,65), Fr (0,68), Pu (0,79), and Po (0,69) suggest a trend to force, power and energy release to determine performance at vmax. Once Eanaer became constrained, only economy was able to accommodated to these context (-0,95), whereas emec improve their influence on Fr (0,97), Pu (0,90), and Po (0,98). In conclusion, work rate is the main parameter to ensure supramaximal performance, and Eanaer is the major factor in power availability, but when it is constrained, emec and economy interactions plays a fundamental role to maintain the level of work rate production enough to reach supramaximal swim requirements.

Estimation of postmortem interval with multivoxel-voxel proton 1H-MR spectroscopy / 法医学杂志

OBJECTIVE@#The purpose of our study was to evaluate the postmortem interval with multi-voxel 1H-MR spectroscopy.@*METHODS@#Twelve healthy rabbits were studied and the quantities of N-acetylaspartate, total choline, phosphocreatine and creatine were measured by 1H-MR spectroscopy after death at 0.5, 1, 2, 4, 6, 8, 12, 16, and 24 h.@*RESULTS@#The levels of Naa/Cr and Naa/Ch decreased following death, while the level of Ch/Cr increased initially and then decreased following death.@*CONCLUSION@#Multi-voxel proton MR spectroscopy for Naa/Cr and Ch/Cr metabolic ratio could be used in future postmortem interval studies.

Estudo do metabolismo energético muscular em atletas por 31P-ERM / Muscular energetic metabolism study in athletes by 31P-MRS

OBJETIVO: Caracterizar as reservas energéticas de metabólitos fosforilados no músculo esquelético de atletas mediante 31P-ERM. MÉTODOS: Amostra deste estudo foi formada por 14 atletas de alto nível do Centro de Alto Rendimento Esportivo (CAR, Sant Cugat del Vallés, Espanha). O padrão de metabólitos fosforilados foi medido no músculo vasto medial por 31P-ERM. A suplementação oral foi realizada durante 14 dias, na forma de 20g de monohidrato de creatina. Os atletas foram determinados conforme as suas características físicas (peso, altura, índice de massa corporal (IMC), consumo máximo de oxigênio (VO2 Max.) em dois grupos: placebo (maltodextrina) e suplementação com creatina. O protocolo de exercício foi realizado no interior do túnel de ressonância (160 x 52 cm), a 60 ciclos por minuto para ambas as pernas. RESULTADOS: Os resultados demonstraram um aumento significativo da fosfocreatina (PCr) durante o exercício, após o período de suplementação, denotando uma redução do seu consumo no grupo que recebeu suplementação com creatina; não houve diminuição significativa do pH intracelular e fosfato inorgânico após a suplementação. CONCLUSÃO: O protocolo de exercício realizado pelos fundistas no Centro de Diagnóstico de Pedralbes permitiu detectar mediante 31P-ERM, no grupo que foi suplementado com creatina, uma diminuição do consumo de PCr durante os períodos de exercício.

Proton Magnetic Resonance Spectroscopic Changes of the Primary Motor Cortex and Supplementary Motor Area in Hemiparetic Patients with Corticospinal Tract Injury due to Deep Intracerebral Hematoma

This study was conducted to investigate the metabolic changes in the motor and motor association cortices following axonal injury in the internal capsule that was caused by deep intracerebral hematoma. Using proton magnetic resonance spectroscopy (1H MRS), the authors studied the primary motor cortices (M-1) and sup-plementary motor areas (SMA) of 9 hemiparetic patients with documentable hemi-paresis of varying severity, and we studied 10 normal volunteers as controls. To measure the M-1 and SMA biochemical changes, 4 separate single volumes of inter-est(VOIs) were located bilaterally in the affected and unaffected hemisphere (AH and UH).1H MRS provided a neuronal and axonal viability index by measuring levels of N-acetylaspartate (NAA) and creatine/phosphocreatine (Cr). The M-1/SMA NAA/Cr ratios of the AH and UH in patients, and the AH and normal volunteers were com-pared. The NAA/Cr ratios of the M-1 and SMA in AH, and the SMA in UH were sig-nificantly lower than those of normal volunteers. These 1H MRS findings indicate that axonal injury in the descending motor pathway at the level of internal capsule could induce metabolic changes in the higher centers of the motor pathway.

Effect of flavone in a canine model of myocardial stunning.

Putative cardioprotective action of flavone (10, 20 and 30 mg/kg) was investigated in a canine model of regional ischemia (20 min) followed by 60 min of reperfusion. In animals pretreated with vehicle, myocardial stunning was evidenced by significant changes in hemodynamic parameters (depressed mean arterial pressure, LV peak (+) dP/dt, LV peak (-) dP/dt and elevated LV end-diastolic pressure) and biochemical parameters (decreased myocardial ATP and rise in plasma malondialdehyde or MDA; a marker of free radical-induced injury). A reduction in plasma MDA was noted with 20 and 30 mg/kg flavone, although attenuation of myocardial dysfunction was evident with all the three doses. The results suggest that besides a significant dose-dependent antioxidant effect, flavone may also have some cardioprotective actions per se, which needs to be further investigated.

Role of Lipistat in protection against isoproterenol induced myocardial necrosis in rats: a biochemical and histopathological study.

A test drug (Lipistat) comprising of equal-proportions of extracts of Terminalia arjuna, Inula racemosa Hook, latex of Commiphora mukul, in three different doses (225 mg/kg; 350 mg/kg; 450 mg/kg) were administered orally daily for 6 days a week for 60 days in rats. Thereafter, the rats were subjected to isoproterenol (ISO) induced (85 mg/kg, s.c. for 2 days) myocardial necrosis. Gross and microscopic examinations (histopathology) were done along with estimations of myocardial tissue high energy phosphates (HEP) stores and lactate content. Gross examination showed significant (P < 0.05) cardioprotection in Lipistat treated animals. On microscopic examination no statistically significant reduction in myocardial damage by 350 and 450 mg/kg of Lipistat were observed although loss of myocardial HEP stores and accumulation of lactate were significantly prevented. The results of the present study suggest the potential usefulness of Lipistat in the prevention of ischemic heart disease.

Anoxia and ischemia tolerance in turtle hearts

It has been known since ancient times that turtle hearts exhibit extraordinary tolerance to anoxia or ischemia. The mechanisms by which they accomplish this remain obscure. The most important adaptation in anoxic turtles is a rapid and dramatic decrease in metabolic rate. Nuclear magnetic resonance measurements indicate that painted turtle (Chrysemys picta) hearts respond to anoxia with a rapid decrease in phosphocreatine (PCr; to 50 percent of control) after which PCr remains constant for at least 4 h. ATP is defended and does not decrease while intracellular pH (pHi) decreases by 0.2 pH units early in anoxia and is then maintained constant. Softshelled turtles (Trionyx spinifer) have been demonstrated to be far more sensitive than painted turtles to anoxia in vivo. However, isolated hearts from softshelled turtles appear to be as anoxia tolerant as those of Chrysemys. During ischemia there is also little difference in cardiac performance, high energy Phosphates, or phi between these two species. A peculiar feature of turtle hearts is an extremely high concentration of phosphodiesters (PDE). The role of cytosolic PDEs remains controversial but they may function as lysophospholipase inhibitors and thereby limit phospholipid turnover (Burt CT and Ribolow H, Comparative Biochemistry and Physiology, 108B: 11-20, 1994). Whether PDEs promote anoxia/ischemia tolerance is unknown but these stresses can result in membrane lipid dysfunction in mammals. Metabolic control, acid-base, and phospholipid homeostasis all play a role in anoxia and ischemia tolerance in turtle hearts. These physiologic processes are interdependent, and how they interact in these animals is unknown, but they are experimentally accessible by modem analytical methods.

Cerebral energy metabolism following ESWL brain injury model and effects of cerebral protective drugs

The goal of this study was to introduce a new method inducing an experimental brain injury model using ESWL(Extracorporeal Shock Wave Lithotripsy) and to evaluate findings of localized lesions on 1H MR imaging and the response of cerebral energy metabolism using a 31P MR spectroscope to the ESWL brain injury in cats. This study also examined effects of cerebral protective drugs. 1) There were no statistically significant changes in pH at all measurement points. 2) In the trauma group, initial decrease of PCr/Pi was seen at 30 to 60 minutes with return to control levels by 2 hours after injury(P < 0.05), followed by a second decline at 4 hours which lasted until 8 hours after injury. 3) Significant recovery in PCr/Pi(P < 0.05) was observed in both the THAM and dexamethasone treated groups at all measurement points and in the mannitol treated group only temporary recovery at 30 and 60 minutes (P < 0.05). 4) High intensity signals were seen on 1H MR imaging in traumatized animals. This study demonstrated the immediate and persistent recovery of cerebral energy metabolism using THAM or dexamethasone and an immediate but transient effect with mannitol in traumatized animals.

Recovery from reperfusion injury in intact canine heart by nifedipine.

Effect of nifedipine post-treatment (100 micrograms/kg slow bolus followed by 3 micrograms/kg/min infusion) on the functional and metabolic changes of the heart after a brief regional ischemia (I) (20 min.) followed by 1 hr of reperfusion (R) was studied in pentobarbitone-anaesthetized open-chest coronary ligated dogs. In the control group, 1 hr of reperfusion failed to cause any significant recovery of the depressed LVdP/dtmax and that of the elevated LVEDP (LVdP/dtmax, pre-ischemic: 2720 +/- 90 mm Hg/sec., 20 min. of I: 2410 +/- 120 mm Hg/sec and 60 min. of R: 2210 +/- 130 mm Hg/sec. LVEDP, pre-ischemic: 5.25 +/- 0.2 mm Hg, 20 min. of I: 10.5 +/- 0.9 mm Hg and 60 min. of R: 7.5 +/- 0.5 mm Hg). However, 1 hr of reperfusion caused a significant recovery of ischemia-induced depletion of myocardial creatine phosphate (CP) content only, but not that of ATP. On post-treatment with nifedipine (i.e., infusion started just before reperfusion), there was a significant recovery in LVEDP (8.25 +/- 0.6 mm Hg after 20 min. of ischemia to 5.0 +/- 0.4 mm Hg after 1 hr of reperfusion) and there was no further deterioration in LVdP/dtmax, as observed in untreated dogs. More significantly, nifedipine caused a near normal recovery of both ATP and CP contents of the affected myocardium. Therefore, the present study shows that post-ischemic administration of nifedipine prevented reperfusion injury of the ischemic myocardium, as evidenced by both functional and metabolic recovery.

Proton liberation in the pre-steady state phase of creatine kinase.

Numerous stereochemical and kinetic investigations on the reaction pathway of creatine kinase (CK) suggest that this enzymic reaction proceeds via direct in-line transfer of phosphate between participating substrates and to date there has been no chemical evidence for any plausible intermediate between enzyme-substrate and enzyme-product complexes. By following the absorption pattern of a pH sensitive dye (o-cresol sulphonaphthalein) in a stopped flow module we have studied transient pH changes in the backward reaction of CK. While the rapid mixing of ADP and CK gives no pH transient, that of phosphocreatine (PCr) and CK gives H+ liberation with kapp of 62.8 sec-1. The magnitude of proton release is one H+ per monomer of CK. Mixing of PCr+CK with ADP does not give any detectable pH transient and the reaction immediately proceeds to steady phase. The mixing of ADP+CK with PCr again gives a release of 1.2 H+ per monomer of CK with kapp of around 67.2 sec-1 before the reaction proceeds to steady phase where there is absorption of one H+ per ADP transphosphorylated. The results obtained, therefore, indicate the involvement of proton deficient E.PCr and E.ADP.PCr complexes in the pathway of CK.