Acute growth hormone response lo low-intensify KAATSU resislclnce exercise: Compclrison between clrm clncJ leg Y. Sclb, A. Yoshilomi′ T. Abe Inf. J. KAATSU TroJ'nJ'ng Res. 2005,・ 1 : 45-50 Exercise is cI POIenl slimulus fo GH secretion. Howeyer iI is uncleclr if exercise-induced GH relec'se differs between different muscle groups′ i.e., clrm Clnd kg exercise′ when performecl cll equiyc'lenl exercise inlensi叶. The purpose of this study WCIS fo compclre the GH responses lo on cICUte resisfclnCe exercise/ Combined with reslriclion of muscuJqr venous blood now (KAATSUいn muscle groups of the qrm ond leg. Fiye young mQle subiecls performed twoサpes of exercise lesls′ orm clnd leg exercise/ on sepQrOIe days. The inlensiサof exercise WCIS 20% 0日-RJ^, which WCIS meqSUred CII lecISI l week before the experiment. The exIerncll reslriclion pressure during the KAATSU exercise WCIS Selected 50% higher Ihc.n ecICh mecISUred-orm ond esIimc'Ied-leg syslolic blood pressure. Venous blood sc,mples were oblc.ined prior lo the slqrf oF exercise′ immediclfely post exercise′ Cnd 1 5- C'nd 60-min Correspondence fo: cIFIer exercise′ clnd blood lcICIole (LA)′ growth hormone (GH)′ norcldrenQline (NA)′ hemcllocrif, Y Sc.fo, DepclrbTtenf of qlbumin c・nd Nc./K concenlrc・Iions were mec・sured. Signifkcnl eJeyqIions were cIPPClrent immedicllely lschemic Circuldlory Physiology, The Uniyersity of post clnd 1 5-min clfrer exercise for LA clnd clI immedicIIely post, 1 5- clnd 60-min clber exercise for GH Tokyo, 7-31l Hongo, Bunkyo- in both clrm Ond Ieg exercise. Significclnt eJeycllion wcls clIso observed clfrer exercise for NA in both ku, Tokyo l l 3-0033, Jqpcln orm qnd leg, but leg exercise resulted in c'grecIIer increcISe in NA Ihcln qrm QI immedicIIely post i nfo@scIIosporIs J=0 , ip See end of cITlicle for cluIhor'clfFili。Iions exercise. ChcLnge in plcISmO YOIume clker exercise WCIS no† differenl between two exercises. These results suggest Ihc.I GH secrefory responses lo exercise mcly be similor between the c'rm clnd leg when performed cll equiyclIenI exercise intensity clnd reslrklion stimulus. Key words: resislclnCe lrclining, growth hormone′ yenous b一ood flow reslriclion′ norqdrenclline l NTRODUCTtON KAATSU-induced GH secretion′ such as muscle It is well established that secretion of human metabolic demands and hypoxia. Although the growth hormone (GH) is stimulated by physical exercise and that exercise-induced increases in precise mechanism is not fully understood′ drculating GH might mediate some of the anabolic from working muscle seem to play an important role in stimulation of KAATSU-induced GH release adaptations induced by exercise′ such as muscle Sympathetic nerve signals sent by metabolic receptors hypertrophy′ bone mineralization′ and local lTakarada etal., 2000; Tdkano etal.′ 2005]. When angiogenesis [Cuneo et a1., 1991; Kelly et al.′ 19901. the activation of chemoreceptors during exerdse is Since exercise-induced GH secretion is, however, proportional to the exercise intensity per unit of related to exerdseintensityina linear dose-response muscle mass′ serum GH responses to acute exerdse lPritzlaff etal., 1999; Schmidt et a1., 2004], it would differ between musde groups of different size. In this seem likely that there would be a greater GH line, GH responses to acute exercise may be greater response after higherintensity physicalexercise. In during lower body exerdse when compared to the linewiththis observation, lowintensity (i.e., regular upper body exerdse. life-style physical activity, 10-20% exerdseintensity) exercise rarely results in increased serum GH concentrations lFelsing et a1., 1992]. However, low- that greater increases in serum GH concentration intensity (∼20% exerdse intensity) exerdse′ when 血an血ose obseⅣed du血g leg exerdses perfomed at combinedwith restriction of venous blood flow from A previousstudy lKodowski et al.′ 1983] reported accompanied arm (smaller muscle group) exercise equivalent oxygen uptake. However,inthat study, the working muscle (lWTSU exercise), has been theintensity of their am exerdse was not similar to reported to substantially Increase Serum GH leg exercise when performed at the same absolute concentrations lAbe et a1., 2005b,・ Takarada et al., oxygen uptake, Since peak oxygen uptake during arm 2000; Takano etal., 2005]. exercise is 30% lower when comparedwith leg A variety of factors are thought to influence the exerdse, resultingina higher exerdseintensity for Acute GH response b KAATSU exercise: Compclrison between orm Cnd leg 46 the am exerdse. Therefore, it is not clear whether Blood sqmpling c]nd biochemiccd cmcllysis resistive exerdse combinedwith orwithout KAATSU Venous blood samples were obtained prior to the would produce differencesinGH secretion between am and leg exerdse perfomed at the same exerdse intensity. Thus, the pulpOSe Ofthe present study was start of exercise, immediately post exercise, and I 5- to compare the GH responses to acute KAATSU resistance exercise in either arm or leg muscle portable analyzer (Lactate Pro, Arkray, Kyoto, Japan) I Serum GH concentration was measured with a eXerCISe. and 601min after exercise. Blood lactate concentrations (LA) Were determined using a commercially available radioimmunoassay (S.R.L Incり Tokyo′ Japan). Plasma noradrenaline SUBJECTS clnd州ETHODS concentration was measured by means of high- Subiecls performance liquid chromatography (HPLC) with Five recreational1y active male volunteers aged 2428 years (26.0 ± 1.8 years) wi血a body mass index of electrochemiCaldetection. Hematocrit was measured induplicate bymicrocentrifugation. Serum albumin 23.6 ± 1.1 kg/m2 were studied. None of the subjects and Na/K concentrations were also measured by had any history of relevant medical illness or were bromcresol purple and by ion-selective electrodes′ taking medication.All subjects wereinformed of the respedvely. Relative change in plasma volume was procedures′ risks′ and benefits′ and signed an calculated in accordance with a previous formula informed consent document before participation. (van Beaumont et alり1973). The Tokyo Metropolitan Urdversity Ethics Cormittee for Human Experiments approved the study. SIclfiSliccII cncllyses Experimentcll design clnd exercise probcols deviation (SD) for all variables. The effects of am Results are expressed as means ± standard The subjects partidpated in two types of exerdse lWTSU-exercise compared to leg KAATSU-exerdse tests on separate dayswithina week interval: 1) arm on changes in blood parameters over time (exerdse exercise (arm curl and triceps press down)′ 2) leg and post-exerdse time) were tested by a two-fador exercise (squat and leg curl). All tests were ANOVA for repeated measurements. Further analysis performed after a 4 h hstinthe aflemoon.Alter 30 used Student's paired t-test if theinteraction, time x min of rest, pre-testing blood samples were collected. group′ was sigrdcant. Statistical significance was set The subjects then performed 30 repetitions of armor at P<0.05. leg exercise of 20% of a p∫e-determined 1-RM. perfomed three sets of 15 repetitions′ with each set RESU LTS Blood lclclc]le, norc]drenclline 。nd growth and exerdse separated by 30 sec rest period. hormone Resfriclion of muscuhr yenous blood flow by for blood LA (P<0.001, Fig.1) and serum GH Followlng a 30 see rest period, the subjects then A sigmificant maineffect for time was determined KAATS U A method for indudng the restridion of muscular (P<0.001, Fig. 3). Post hocanalysesindicated that for the two variables′ slgnificant elevations were venous blood now has been previously reported lAbe apparent immediately post and 1 5-mina丑er exercise et al. 2005a]. Briefly, the subject wore an air pressure for LA and at immediately post, 1 5- and 601minafter belt (30 mmwide for the armand 45 rrmwide for leg, Kaatsu Master, Sato Sports Plaza, Tokyo, Japan) exercise for GH in both arm and leg KAATSUexercise. A signiRcant group x timeinteraction was placed around the most proximal portion on both arms or on both legs during the corresponding Post hoe analyses indicated that leg KAATSU-exercise exerdse. Resting systolic blood pressure (SBP) of the arm(at heart level) was measured using an automatic sphygmomanometer (Fit Cuff, Omron, Tokyo, observed for plasma noradrenaline (P<0.001, Fig. 2). resulted in a slgnificantly greater increase in noradrenaline levels when compared to arm lWTSU-exerdse immediately post exerdse. Japan)′ and SちP of the leg was estimated as follow: leg SBP = 120% of arm SBP. The extemal restriction pressure was selected 50% higher than each of the SBP, i.C.′ 190 mmHg for arm and 230 mmHg for leg, P(】rclmeTers of plcISmCI YO-ume chclnge A sigmincant maineffect for time was observed for limbgirth (P<0.001)and hematocrit (P<0.001, Table when am SBP is l25 mmHg. Restriction of musde 1). Post hoc analyses indicated that upper-am and blood flow was maintained for the entire exercise thighgirths wereincreased immediately post, and I 51 session, including the rest periods. The belt pressure and 60-min after exercise. AIso′ hematocrit was was then released immediately upon completion of elevated immediately post exercise followlng both the session. trialS′ and I 5-mina允er exerdse during armKAATSUexerdse. A sigmi丘cant group x timeinteraction was observed for serumalbumin concentration (P=0.037), 47 Y. ScIIo′ A. Yosh汁omi, T, Abe 1 1 2 0 8 (l\tOtHu)at ZTUtZTpO t円 ノb 4 (ノ】 pre post after 1 5 after60 FigtJre 1. Blood lactate concentrationsinresponse to acute lowintensity resistance exercise combined with KAATSU. Significant differences from pre-exerdse, ** p < 0.01. (t HJgu)au!TtmaJPtZJOtl ?uSPTd LJ'ノ O LJ.1 2 2 1 pre post after 1 5 after60 Figure 2. Plasma noradrenaline concentrationsinresponse to acute low-intensity resistance exercise combined with KAATSU. SigniBcant differences from pre-exercise′ * p < 0.05, ''p < 0.01, SigniBcant difference between armand leg exercise′ † P < 0.01. Acute GH response to KAuATSU exercise: Compclrison between clrm ClnCl leg 48 Tclble 1. Limbgirth′ hematocrit′albu血l and Na/K concentrationsinresponse to acute low- intensity resistance exerdse combinedwithlWTSU Pre Post 1 5 1min 60 -min Arm Upper arm girth (cm) 30.0(1.4) 32.2 (1.9)†31.8(1.6)†31.1 (1.6)千 Hematocrit ( % ) 43.5 (0.7) 49.5 (1.2)†45.6 (1.ラ)* 44.0 (0.5) Na (m】∃q/L) 141 (2) 142 (ラ) 140 (2) 141 (2) K (m】∃q/L) 4.5(0.4) 3.9(0.ラ) 3.9(0.2) 4,4(0.5) Albumin (g/dl) 5_I(0.4) 5.9(0.3)i' 5.2(0.3) 4.9(0.2) Leg Thigh girth (cm) 56.0 (2.7) 58.0 (2.7)† 57.2 (2.5)千 56.9 (2.5)† Hematocrit (%) 44.9 (1.2) 49.7 (1.1)†46.4 (2.2) 44.9 (0.9) Na (mEq/L) K (mEq/1) 4.1(0.3) 3.9(0.4) 4.0(0.7) 4.5(0.6) Albumin (g/dl) 5.1(0.2) 5.7(0.2)† 5.4(0.1)* 5.0(0.2) 141 (2) 144(3) 142 (2) 141 (1) Significant differences from pre-exercise, 'p<0.05 †P<0.01 (tuJgu)auouJOq t臣OJStXmJaS つつ つつ LJ1 0 LP. nU 2 つム 0 pre post after lう after60 Figure 3. Serum growthhormpne concentrationsinresponse to acute low-intensity resistance exercise combined with KAATSU. Significant differences from pre-exerdse′ * p < 0.05 ** p < 0.01. however a post hoc analyses showed no significant exerdse. Our丘ndings demonstrated that the notable differences over time. Relative change in plasma volume after exerdse was not significantly different increases in serum GH response to resistive exerdse with KAATSU was observed in both arm and leg between am (-21%) and leg卜17%) exerdse. exercise. Furthermore, there was no significant DISCUSStON difference between the muscle groups in GH response. In addition, the magnitude onheincreases It is Weu known that exerdse is a potent stimulus imam and leg exerdse was consistentwith previous for GH secretion′ especially high-intensity exerdse. IWTSU studies [Takarada etal., 2000; Takano et a1., However, it is not clear whether exerdse-induced GH 2005]. h contrast′ a previous study 【Kozlowski et al.′ release differs between upper-body and lower-body 1983] reported a greater increase in plasma GH 49 Y. Sclb′ A. Yoshilomi′ T. Abe Concentration following arm exercise when previous reports [Giustina and Veldhuis′ 1998; compared to leg exercise performed at equlValent Weltman et al.′ 2000】′ but at the same time, support absolute oxygen uptake. However,inthat study, the the concept that theincrease in plasma noradrenaline relative exercise intensity for the arm was higher after exerdse depends on the size of the muscle mass compared with leg exercise′ since peak oxygen utilized [Seals and Victor′ 1991】. It is clear that uptake du血g am exerdse is 30% lower than that of further studies are needed to clarify the basic leg exerdse lSanada et a1., 2005]. In fact′ Kozlowski mechanisms of GH release that is stimulated by arm and colleagues (1983) reported a greaterincreasein or leg KAArSU exerdse. heart rate and blood lactate concentration du血g and In conclusion, there were no sigmi丘cant difference after血e am exerdse compared with those of the leg in serum GH concentrations fouowing arm and leg exercise. Therefore the difference in exercise intensity between the armand leg exerdse, and not KAATSU exercise. These results suggest that exercise-induced GH secretion may be similar any int血sic difference between muscle groups per between the arm and leg exercise performed at se′ may be the reason for the larger GH response in equivalent exerciseintensity and restriction stimulus. am exerdse. h me present study. usmg an exerdse intensity of 20% of I-RM and a restriction stimulus of 150% of resting systolic blood pressure to the Referent:eS working musde resultedinsiユldar GH responses for Abe T, YosUdcI T,仙dorikcIWCI T, ScIIo Y, KeclrnS CF, lnoue K, Koizumi both the arm and leg exerdse. Our results suggest that the GH secretory responses to exerdse may be K, Ash-li N (2005cl) SkeletcIl muscle size clnd circUlclIing lGF-1 ore increcISed clber Two weeks oF twice dclily 〝KAATSU〝 resistclnCe lrclining. similar between musde groups of different size when lnfJ KAATSU Trclining Res 1 : all 2. perfomed at equlValent exerdse intensity. Abe T′ KeclrnS CF, Scllo Y′ YoshH・omi A (2005b) Acute hormoncll In the present study, We found that post exerdse responses to reslricIion oHeg muscle blood flow during wcllking blood lactate concentrations were similar between (AbsfrcICl). 川ed Sci Sports Exerc 37: Sl 08. arm and leg exercise with KAATSU. These results CLIneO RC′ ScILomon F′ Wiles CM, Hesp R, Sonksen pH (1 991 ) Growrh suggest that blood lactate could serve as a marker for exercise-induced GH release, Since there was a similar increaseinGH observed after exercise. However, a hormone lrecllmenl in growth hormone-deficient cldUlls. ll. Effects on exercise performclnCe. J Appl physiol 70: 695-700. Felsing NE, Brc-sel JA′ C∞per DIvH1 992) Effect oHow clnd high inlensiサ exercise on circULclling growth hormone in men. J CIin Endocrinol仙elclb previous study [Luger et al.′ 1992】 reported血e effect 75: 157-162. of sodium Llactate intravenous infusion on plasma Giuslinc] A, Veldhuis JD H 998) Pcllhphysiologicc'l bc'sis oF the GH concentration (doses producing blood lactate concentrations within the range of those seen clnd the hUmcln. Endocrine Rey l 9: 71 7-797. neuroregulcllion of the somcllotropic (GH) C'xis in experimenlcII Qnimclls Ke"y pJ, Eismcm JA′ SIuclrt MC′ Poc∝k NA′ Sc'mbrook pN, Gwinn TH between 70% and 90% Vo2max)′ and found that the elevation of plasma GH was smaller than those 日990I Somc'Iomedin-C, physiccll fitness′ C'nd bone density. J Clin EndocrinoI MefcIb 70: 71 8-723. obtained at an exercise-induced matched blood Kozlowski S, Chwc'lbinskc-lMoneIcI J′ VigcIS M, KcIdubcl-UsciLko H, lactate concentration. Changes in blood lactate and Nc'zc-r K (1 9837 Greclter serum GH response to clrm thcln rO leg exercise catecholamine release followed similar patterns of performed cll eqUiycllenl oxygen uplclke. Eur J AppI Physiol 52: 1 3l 135. response to exerdse 【Weltman et al.′ 1994; Sclmeider et a1., 2000], therefore, it is unlikelythat blood lactate itself is responsible for the GH response to KAATSU exerdse and would be a poor surrogate marker for GH. Noradrenaline is one of several markersthat have Luger A, Wcllschinger B′ Deusler P, Svobodc'T, CLodi M, Chrousos GP 日992) PIcISmCl growth hormone cfnd prolcIdin responses lo grclded leyels of cICUIe exercise clnd to cl lqclclte infusion. NeUroendocrinology 56: 112-117. PriTzJclff CJ′ WidemcHI L′ Wellmcln JY, Abbo什RD, GuIgesell ME, Hclrlmcln J^L, Veldhuis JD′ Wellmcm A (1 999日mpcId of cICUte eXerdse been suggested as an explanation for exercise- inlensiサon pulsclrile gro叫h hormone reLec-se in men. J Appl physiol 87: induced GH release. For example, invitroanimal 498-504. studies found that catecholamines can directly SclncdtコK, Kecms CF, KoiimcI K′ Abe T (2005) Peclk oxygen uplclke stimulate GH secretion from pituitary tissue lGiustina and Veldhuis′ 1998】. In humans′ when exercise intensity is increased from 25% to 175% of an individual′s lactate threshold′ the change in serum GH is linearly related to changes in plasma during running c'nd c-rm crc'nking normqlized Io lolc-L clnd regioncll skeletol muscle mcISS meCISUred by mclgnelic resonclnCe imclging. Eur J AppI Physiol 93: 687-693. SchrnidI A, Mc-ier C, Schclller G, Nowolny P, Bclyerle-Eder lvt, Burcmyi B, Luger A′ WolzI ∼ (2004I Acule exercise hcLS nO effect on ghrelin plcISmCI COnCenlrolions. Horn Melclb Res 36: 1 74-1 77. noradrenaline concentrations lWeltman et a1., 2000]. Schneider DA,仙cLe"cln TJ^, GcISS GC (2000) PIQSmCI CCIIecholdmine In the present study′ however′ noradrenaline clnd blood lc'clqle responses to incrementcll c'rm qnd Leg exercise. Ned concentrations were slgnificantly lower in the arm Sci Sports Exerc 32: 608-61 3. exerdse thaninthe leg exercise′ despite the fact that there was no differenceinGH responses betweenthe arm and leg exercise. Our findings differ from Seas DR′ Vicror RG (i 991 ) Regulcllion oF muscle sympcllheIic nerve c-。ivity during exercise in humclnS. Exerc Sports Sci Rey 19: 31 3-349. Tokclno H, J^or汁cI T′ lidcI H, AscldcI K, Kcllo J^, Uno K, Hirose K, el CIL (2005J Hemodynclmic clnd hormoncII responses lo cI ShorHerm low- 50 Acute GH response to KAATSU exercise: Compc・rison between c・rm c.ncE leg inlensiサresisrQnCe exercise with the reduction of muscle blood flow. EUr Welfmcln A, Pritzlclff cJ, Wdemcln L, Welfmcln JY, BIumer JL, Abbott J AppI PhysioJ (in press). RD′ Hc.rImc.n ML, Veldhuis JD (2000I Exercise-dependent growth Tc・kく】rOd(】 Y, Nc.kc,murc・ Y′ ArUgcI S, OndcI T′仙ycIZClki S′ Ishii N hormone release is linked fo m。rkers of heightened cenlrd cldrenergic (2000) RcIPid increcISe in pkISmO grOWIh hormone Offer low-intensify resislc・nce exercise with vcISCUIor occlUsion. J Appl physiol 88: 6l -65. ouIRow. J AppI Physiol 89: 629-635. vcn BecumonI W′ SIrc.nd JC, Pelrofsky JS, Hipskind SG′ GreeniecIF JE (1 973I Chc・nges in lolc.l plcISmC・ COnlenl of electrolytes clnd proleins with Aulhors'clffiliclfions mcIXimc,l exercise. J AppI physio1 34: 102-lob. Y・ Sc血, Depc.rTmenl oHschmic CirculclrOry Physiology′ The Uniyersi∼ of WeLIm。n A, Wood CM, WomcICk CJ, DcIYis SE′ BIUmer JL, ALyclreZ J, Tokyo, Tokyo, JcIPQn ScIUer K′ Goesser GA H 994I Colecholomine clnd b一ood loclclle A. Yoshilomi′ T. Abe, Deportmenl of Exercise ond Sport Science, responses 也 incremenlc.I rowing c.nd running exercise・ J AppI Physio1 Tokyo仙elropolibn Universiサ′ Tokyo, JcIPC-n 76: 1 144-1 149.
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