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Education  |   March 2004
Effect of Amino Acid Infusion on Central Thermoregulatory Control in Humans
Author Affiliations & Notes
  • Yasufumi Nakajima, M.D., Ph.D.
    *
  • Akira Takamata, Ph.D.
  • Takashi Matsukawa, M.D., Ph.D.
  • Daniel I. Sessler, M.D.
    §
  • Yoshihiro Kitamura, M.D., Ph.D.
    *
  • Hiroshi Ueno, M.D.
    *
  • Yoshifumi Tanaka, M.D., Ph.D.
  • Toshiki Mizobe, M.D., Ph.D.
    #
  • * Instructor, ∥ Professor and Chair, # Associate Professor, Department of Anesthesiology, Kyoto Prefectural University of Medicine. † Associate Professor, Department of Environmental Health, Nara Women’s University. ‡ Associate Professor, Department of Anesthesia, University of Yamanashi, Faculty of Medicine. § Associate Dean for Research, Director Outcomes Research™ Institute, Lolita & Samuel Weakley Distinguished University Research Chair, Professor of Anesthesiology and Pharmacology, University of Louisville.
  • Received from the Department of Anesthesiology, Kyoto Prefectural University of Medicine, Kyoto, Japan; the Department of Anesthesia, University of Yamanashi, Yamanashi, Japan; the Department of Environmental Health, Nara Women’s University, Nara City, Japan; and the Outcomes Research™ Institute and Departments of Anesthesiology and Pharmacology, University of Louisville, Louisville, Kentucky.
Article Information
Education
Education   |   March 2004
Effect of Amino Acid Infusion on Central Thermoregulatory Control in Humans
Anesthesiology 3 2004, Vol.100, 634-639. doi:
Anesthesiology 3 2004, Vol.100, 634-639. doi:
INTRAOPERATIVE core temperature depends both on distribution of heat within the body and on systemic heat balance. During the first hour of anesthesia, core-to-peripheral redistribution of heat is the primary cause of core hypothermia. 1 Subsequently, however, hypothermia results from heat loss exceeding heat production. 2 Core temperature during this second phase of the hypothermia curve therefore depends on systemic heat balance. Because anesthetics profoundly impair thermoregulatory control, 3,4 factors that increase thermogenesis or reduce loss of heat to the environment moderate the rate at which intraoperative hypothermia develops. 5–7 
Ingestion of glucose or fat only minimally increases the metabolic rate. However, enteral or parenteral administration of protein or an amino acid mixture stimulates oxidative metabolism, typically increasing the metabolic rate approximately 20%. 8,9 This postprandial hypermetabolism far exceeds the obligatory metabolic cost of digestion, absorption, processing, and storage of administered nutrients. 10 As might therefore be expected, thermogenesis associated with amino acid infusions have been shown in numerous studies to help preserve intraoperative core temperature 5,11 and to moderate complications associated with hypothermia. 12–14 
An interesting consequence of the hypermetabolism associated with protein ingestion or amino acid infusion is that each increases core temperature, even when thermoregulation remains intact (i.e.  , in unanesthetized volunteers). 8,9 Although hyperthermia might seem to be a logical consequence of hypermetabolism, this is the case only in the absence of effective thermoregulatory control (e.g.  , during anesthesia) because thermoregulatory defenses normally maintain core temperature despite alterations in heat production or heat loss. A single light cotton blanket, for example, reduces heat loss by approximately 30%, 15 which improves systemic heat balance more than the hypermetabolism associated with protein or amino acid administration. However, a blanket does not normally provoke hyperthermia because thermoregulatory defenses maintain core temperature.
The observation that hyperthermia results from protein ingestion or amino acid infusion in volunteers with intact thermoregulation suggests that these treatments produce a regulated increase in core temperature. Thermoregulatory defenses are best characterized by their thresholds (core temperature triggering defense activation) and gain (incremental increase in response intensity as core temperature deviates from the threshold). The major thermoregulatory defenses in humans are sweating, active precapillary vasodilation, arteriovenous shunt vasoconstriction, and thermogenesis. 16 A synchronous change in all autonomic thresholds can be considered a set point alteration. Therefore, we tested the hypothesis that an amino acid infusion increases the thermoregulatory set point.
Materials and Methods
With approval by the Review Board on Human Experiments of Kyoto Prefectural University of Medicine (Kyoto, Japan), written informed consent was obtained from nine healthy men. Their average age was 26 ± 6 yr, their body weight was 69 ± 3 kg, and their height was 172 ± 6 cm (mean ± SD).
Protocol
Each volunteer participated on 4 different study days, separated by at least 6 days. We tested autonomic thermoregulatory responses to external heating and cooling (designated as the heat test and the cold test) after amino acid infusion and saline infusion. The order of the experiments was randomized. To avoid circadian variations, the studies started at 09:00 each day. Volunteers refrained from salty food and beverages containing caffeine or alcohol beginning the night before the experiment. They were not allowed to eat breakfast but could drink water.
After voiding, subjects entered a chamber in which ambient temperature was maintained at 28°C and relative humidity was maintained at 30%. Each subject wore only thin cotton trunks. A 22-gauge intravenous catheter was inserted in an antecubital vein for the administration of amino acids. Another 22-gauge intravenous catheter was placed in a contralateral antecubital vein for blood sampling. Throughout each study day, the volunteers assumed an upright sitting position, leaning against a backrest.
After a 30-min rest period during which baseline data were collected (table 1), amino acid (Teruamino 12, a mixture of 18 amino acids, 18 gN2/l; Terumo, Tokyo, Japan) or saline infusion was given for 150 min/randomization. The solutions were given at a rate of 2 ml · kg−1· h−1, which corresponded, in the case of amino acid, to 4 kJ · kg−1· h−1. Subjects were monitored during the infusion and for 60 subsequent minutes. Depending on the randomization, the participants were then either warmed or cooled.
Table 1. Baseline Values (before Saline or Amino Acid Infusion)
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Table 1. Baseline Values (before Saline or Amino Acid Infusion)
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Warming consisted of the volunteers immersing their lower legs into water at 42°C. Leg heating was maintained until active vasodilation and sweating were observed. Ambient temperature was maintained at 28°C, with a relative humidity of 30% during warming. Alternatively, the volunteers were warmed with a water-perfused suit that covered the entire body except the face, head, forearm, and fingers. Warm water (approximately 40°C) was circulated through the water-perfused suit for approximately 10 min until active cutaneous vasodilation was observed. Core temperature was then decreased at a rate of approximately 2°C/h by reducing mean skin temperature approximately 7.0°C/h by progressively reducing the circulating-water temperature. Cooling continued until vasoconstriction and vigorous shivering were observed, a process that typically took approximately 70 min. Ambient temperature was maintained at 18°C, with a relative humidity of 30% during cooling.
Measurements
Core temperature was measured in the distal esophagus with a thermocouple probe in polyethylene tubing (PE-90; Clay Adams, Parsippany, NJ) that was positioned at a distance of one fourth of the subject’s standing height from the external nares. 17 Skin temperature was measured on the forehead, chest, back, forearm, thigh, and calf. Forearm skin temperature was measured on the noninfused arm. Mean skin temperature was calculated from the body surface area distribution and thermal sensitivity of each skin area. 18 
Heart rate was continuously monitored using an electrocardiogram recorder, and blood pressure was measured every 5 min in the noninfused arm (model STBT-780; Colin, Nagoya, Japan). Mean arterial pressure was calculated as (SBP/3)+DBP, where SBP is systolic blood pressure and DBP is diastolic blood pressure.
The sweating rate on the chest was estimated using a ventilated capsule. Anhydrous air was flushed across a 6-cm-diameter circle of skin surrounded by an airtight adhesive ostomy appliance at a rate of 2.0 l/min. Cutaneous water loss was calculated from the gas flow rate, gas temperature, and relative humidity (HMP233 L; Visala, Helsinki, Finland). The sweating rate on the chest was expressed as mg · cm−2· min−1. This is a well-established method. 19 
Skin blood flow was assessed with a laser-Doppler flowmeter (ALF21; Advance, Tokyo, Japan) on the noninfused forearm during heating and on the noninfused middle finger during cooling. 17 Cutaneous vascular conductance was calculated from the output voltage indicated by the laser-Doppler flowmeter and mean arterial pressure, which was presented as the percent change from the mean value obtained before heating or cooling.
Oxygen consumption is the most reliable method of quantifying thermogenesis. 20 Oxygen consumption was therefore determined at 1-min intervals using a flow/gas analyzer (Aeromonitor AE260; Minato, Tokyo, Japan).
Blood samples were collected before the amino acid (or saline) infusion started, immediately after completion of the infusion, and 1 h after completion of the infusion (before heating or cooling). Plasma aliquots for the measurement of hormone concentrations were centrifuged at 4°C and stored at −80°C until the hormone and amino acid assays were performed. To determine free plasma amino acid concentrations, high-performance liquid chromatography (JLC-300V; JEOL, Tokyo, Japan) was performed using the ninhydrin method. The detection limit of the assay was 1 nm, and the intraassay and interassay coefficients of variation were less than 3%. Catecholamine concentrations were also determined by high-performance liquid chromatography (HLC-725CA; Tosoh, Tokyo, Japan) using an electrochemical detector after alumina extraction. The detection limit of the assay was 8 pg/ml, and the intraassay and interassay coefficients of variation were less than 5%.
Data and Statistical Analysis
The core temperature thresholds for sweating, vasodilation, and thermogenesis were defined by the core temperatures triggering sustained sweating, forearm cutaneous vascular conductance, and total body oxygen consumption increases of 25% above baseline values. 4,21 The core temperature threshold for vasoconstriction was defined by the core temperature triggering a reduction in fingertip-skin vascular conductance to at least 50% of the baseline value. 22 The threshold was individually determined for each condition in each subject by the same inspector who was blinded to the experimental conditions. Thermal responsiveness (gain) was defined by the slope of the linear portion of each thermoregulatory response above or below the threshold core temperature and was calculated by least-squares linear regression on an individual basis.
To compare thresholds between conditions in which both core temperature and mean skin temperature were changing, the following equation was used to correct the core temperature (Tc) for a designated mean skin temperature (T̄SK):EQUATION
where designated T̄SKwas set as 34°C, and β was the fractional contribution of the skin to the vasoconstriction and shivering response (0.2) and to the vasodilation and sweating response (0.1). This methodology is well established. 4 
Morphometric data, thresholds, and thermal responsiveness were analyzed by two-tailed paired t  tests. The effects of amino acid infusion on the cardiovascular, temperature, and metabolic responses were analyzed by a general linear regression model for analysis of variance with repeated measures (two within, zero between factors), followed by Student-Newman-Keuls multiple comparison tests. All data are reported as mean ± SD; P  < 0.05 was considered statistically significant.
Results
Cardiovascular, thermal, metabolic, and plasma catecholamine variables were similar before saline or amino acid infusion (table 1). Amino acid infusion increased core temperature by 0.3 ± 0.1°C and oxygen consumption by 18 ± 12%. Mean arterial pressure, heart rate, mean skin temperature, and plasma epinephrine and norepinephrine concentrations did not differ significantly during infusion of amino acid or saline (data not shown). Core temperature stabilized within 1 h after the infusion was completed. Table 2shows plasma amino acid concentrations before infusion, immediately after completion of the amino acid infusion, and 1 h later. Plasma amino acid concentrations 1 h after completion of the amino acid infusion decreased toward baseline values, indicating that the amino acids were metabolized.
Table 2. Plasma Amino Acid Concentrations (nM/ml)
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Table 2. Plasma Amino Acid Concentrations (nM/ml)
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During warming, core temperature increased at a rate of 0.6 ± 0.3°C/h with the saline infusion and 0.4 ± 0.3°C/h with the amino acid infusion. During cooling, calculated core temperature decreased at a rate of 1.7 ± 0.6°C/h with the saline infusion and 2.3 ± 0.6°C/h with the amino acid infusion. Sweating rate, active cutaneous vasodilation, oxygen consumption, and cutaneous vasoconstriction as a function of calculated core temperature are shown in figures 1 and 2.
Fig. 1. Sweating rate on chest (SRch; top  ) or forearm cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 1. Sweating rate on chest (SRch; top 
	) or forearm cutaneous vascular conductance (CVC; bottom 
	) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 1. Sweating rate on chest (SRch; top  ) or forearm cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
×
Fig. 2. Oxygen consumption (V̇o2; top  ) or fingertip cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 2. Oxygen consumption (V̇o2; top 
	) or fingertip cutaneous vascular conductance (CVC; bottom 
	) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 2. Oxygen consumption (V̇o2; top  ) or fingertip cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
×
Mean skin, core temperatures at the onset of each thermoregulatory response, the thresholds calculated from these values, gains, and hemodynamic responses are summarized in table 3. Amino acid infusion increased the calculated core temperature threshold for active cutaneous vasodilation by 0.3 ± 0.3°C, for sweating by 0.2 ± 0.2°C, for thermoregulatory vasoconstriction by 0.3 ± 0.3°C, and for thermogenesis by 0.4 ± 0.5°C compared with saline infusion. In contrast, amino acid administration did not alter the gain of any thermoregulatory defense.
Table 3. Mean Skin Temperatures, Core Temperatures, Calculated Thresholds, and Gains
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Table 3. Mean Skin Temperatures, Core Temperatures, Calculated Thresholds, and Gains
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Discussion
It is well established that amino acid infusion provokes thermogenesis 5,11 and hyperthermia, 9 and our results confirm previous observations. However, our results also indicate that amino acid infusion synchronously increases the triggering threshold for all major autonomic thermoregulatory defenses in humans, which is equivalent to a set point increase. Therefore, amino acids influence both peripheral heat production and central thermoregulatory control.
Synchronous increases in each of the major autonomic thermoregulatory thresholds suggest an alteration in central thermoregulatory function rather than the summation of individual peripheral actions related to each thermoregulatory defense. The mechanisms by which amino acid infusion increases the set point were not addressed in this study and remain unknown. However, peripherally infused amino acids are unlikely to cross the blood–brain barrier. It is therefore unlikely that amino acids directly alter central thermoregulatory control.
One potential mediator is the sympathetic nervous system. This is relevant because the thermic effects of nutrition are divided into an obligatory component, which represents the theoretical metabolic costs for processing and storing ingested nutrients, and a facultative component, which augments systemic energy expenditure and is reportedly attributable to central activation of the sympathoadrenal system. 23–25 However, intravenous administration of amino acid solutions to tetraplegic patients causes a normal or even supranormal increase in metabolic rate, even though pathways connecting the brain with the peripheral sympathetic nerve pathways to the brain are severed in these patients and they typically exhibit low peripheral sympathetic nervous system activity. 26 Plasma epinephrine and norepinephrine concentrations did not increase after amino acid infusion in our volunteers. Furthermore, increased hypothalamic catecholamine concentrations are associated with hypothermia rather than hyperthermia. 27,28 Taken together, these data suggest that amino acids do not increase the thermoregulatory set point by activating the sympathoadrenal system.
An additional mechanism by which amino acid infusion might increase the thermoregulatory set point is via  metabolites that alter central thermoregulatory control. Alternatively, amino acid infusion might activate peripheral receptors and thus afferent pathways. This possibility is by no means unprecedented: for example, the pyrogenic effect of many cytokines is mediated via  the vagus nerve. 29,30 Although the hyperthermia associated with amino acid infusion resembles fever in being a set point increase, it is presumably not mediated by endogenous pyrogens and cannot be blocked by prostaglandin inhibitors such as acetaminophen. 31 Hyperthermia associated with amino acid infusion also differs from the temperature elevation associated with exercise that simultaneously reduces the sweating threshold. 32 In contrast, the synchronous elevation of all major autonomic thermoregulatory thresholds is reminiscent of the menstrual cycle and circadian rhythm, both of which produce similar increases in the set point. 33,34 Our current results are consistent with the observation that an amino acid infusion increases the threshold for vasoconstriction during spinal anesthesia. 11 
Hyperthermia in response to amino acid infusion has been considered a passive response to hypermetabolism and the resulting thermogenesis. This interpretation is likely correct during anesthesia when thermoregulatory defenses are profoundly impaired. 16 However, it is interesting to note that the increase in core temperature was identical to the increase in set point. Furthermore, with either saline or amino acid infusion, measured core temperatures were virtually identical during warming and cooling. That core temperature did not decrease during intense cooling (and therefore considerable heat loss) indicates that core temperature was actively maintained with vasoconstriction and thermogenesis according to the central thermoregulatory control. This conclusion is consistent with the general theory that, over a wide range of metabolic rates and ambient environments, central thermoregulatory processing dominates control of core temperature.
In summary, amino acid infusion increased both metabolic rate and resting core temperature. However, amino acids also produced a synchronous increase in all major autonomic thermoregulatory defense thresholds (i.e.  , a set point increase), and the increase in core temperature was identical to the set point increase. In subjects with intact thermoregulatory defenses, it is likely that amino acid–induced hyperthermia results from a set point increase rather than an augmented metabolic rate per se  .
References
Matsukawa T, Sessler DI, Sessler AM, Schroeder M, Ozaki M, Kurz A, Cheng C: Heat flow and distribution during induction of general anesthesia. A nesthesiology 1995; 82: 662–73Matsukawa, T Sessler, DI Sessler, AM Schroeder, M Ozaki, M Kurz, A Cheng, C
Kurz A, Sessler DI, Christensen R, Dechert M: Heat balance and distribution during the core-temperature plateau in anesthetized humans. A nesthesiology 1995; 83: 491–9Kurz, A Sessler, DI Christensen, R Dechert, M
Xiong J, Kurz A, Sessler DI, Plattner O, Christensen R, Dechert M, Ikeda T: Isoflurane produces marked and non-linear decreases in the vasoconstriction and shivering thresholds. A nesthesiology 1996; 85: 240–5Xiong, J Kurz, A Sessler, DI Plattner, O Christensen, R Dechert, M Ikeda, T
Matsukawa T, Kurz A, Sessler DI, Bjorksten AR, Merrifield B, Cheng C: Propofol linearly reduces the vasoconstriction and shivering thresholds. A nesthesiology 1995; 82: 1169–80Matsukawa, T Kurz, A Sessler, DI Bjorksten, AR Merrifield, B Cheng, C
Sellden E, Branstrom R, Brundin T: Augmented thermic effect of amino acids under general anaesthesia occurs predominantly in extra-splanchnic tissues. Clin Sci 1996; 91: 431–9Sellden, E Branstrom, R Brundin, T
Hynson J, Sessler DI: Intraoperative warming therapies: A comparison of three devices. J Clin Anesth 1992; 4: 194–9Hynson, J Sessler, DI
Nakajima Y, Mizobe T, Takamata A, Tanaka Y: Baroreflex modulation of peripheral vasoconstriction during progressive hypothermia in anesthetized humans. Am J Physiol Regul Integr Comp Physiol 2000; 279: R1430–6Nakajima, Y Mizobe, T Takamata, A Tanaka, Y
Brundin T, Wahren J: Influence of a mixed meal on splanchnic and interscapular energy expenditure in humans. Am J Physiol 1991; 260: E232–7Brundin, T Wahren, J
Brundin T, Wahren J: Effects of i.v. amino acids on human splanchnic and whole body oxygen consumption, blood flow, and blood temperatures. Am J Physiol 1994; 266: E396–402Brundin, T Wahren, J
Jequier E: Thermogenesis induced by nutrient administration in man. Infusionsther Klin Ernahr 1984; 11: 184–8Jequier, E
Kasai T, Nakajima Y, Matsukawa T, Ueno H, Sunaguchi M, Mizobe T: Effect of preoperative amino acid infusion on thermoregulatory response during spinal anaesthesia. Br J Anaesth 2003; 90: 58–61Kasai, T Nakajima, Y Matsukawa, T Ueno, H Sunaguchi, M Mizobe, T
Sellden E, Lindahl SG: Postoperative nitrogen excretion after amino acid-induced thermogenesis under anesthesia. Anesth Analg 1998; 87: 641–6Sellden, E Lindahl, SG
Sellden E, Lindahl SG: Amino acid-induced thermogenesis reduces hypothermia during anesthesia and shortens hospital stay. Anesth Analg 1999; 89: 1551–6Sellden, E Lindahl, SG
Widman J, Hammarqvist F, Sellden E: Amino acid infusion induces thermogenesis and reduces blood loss during hip arthroplasty under spinal anesthesia. Anesth Analg 2002; 95: 1757–62Widman, J Hammarqvist, F Sellden, E
Sessler DI, Schroeder M: Heat loss in humans covered with cotton hospital blankets. Anesth Analg 1993; 77: 73–7Sessler, DI Schroeder, M
Sessler DI: Perioperative hypothermia. N Engl J Med 1997; 336: 1730–7Sessler, DI
Takamata A, Nagashima K, Nose H, Morimoto T: Osmoregulatory inhibition of thermally induced cutaneous vasodilation in passively heated humans. Am J Physiol 1997; 273: R197–204Takamata, A Nagashima, K Nose, H Morimoto, T
Nadel ER, Mitchell JW, Stolwijk JA: Differential thermal sensitivity in the human skin. Pflugers Arch 1973; 340: 71–6Nadel, ER Mitchell, JW Stolwijk, JA
Washington D, Sessler DI, Moayeri A, Merrifield B, Prager M, McGuire J, Belani K, Hudson S, Schroeder M: Thermoregulatory responses to hyperthermia during isoflurane anesthesia in humans. J Appl Physiol 1993; 74: 82–7Washington, D Sessler, DI Moayeri, A Merrifield, B Prager, M McGuire, J Belani, K Hudson, S Schroeder, M
Hong SI, Nadel ER: Thermogenic control during exercise in a cold environment. J Appl Physiol 1979; 47: 1084–9Hong, SI Nadel, ER
Mack G, Nishiyasu T, Shi X: Baroreceptor modulation of cutaneous vasodilator and sudomotor responses to thermal stress in humans. J Physiol 1995; 483( pt 2): 537–47Mack, G Nishiyasu, T Shi, X
Frank SM, Raja SN, Bulcao C, Goldstein DS: Age-related thermoregulatory differences during core cooling in humans. Am J Physiol Regul Integr Comp Physiol 2000; 279: R349–54Frank, SM Raja, SN Bulcao, C Goldstein, DS
Landsberg L, Young JB: Fasting, feeding and regulation of the sympathetic nervous system. N Engl J Med 1978; 298: 1295–301Landsberg, L Young, JB
Astrup A, Bulow J, Christensen NJ, Madsen J, Quaade F: Facultative thermogenesis induced by carbohydrate: A skeletal muscle component mediated by epinephrine. Am J Physiol 1986; 250: E226–9Astrup, A Bulow, J Christensen, NJ Madsen, J Quaade, F
Astrup A, Simonsen L, Bulow J, Madsen J, Christensen NJ: Epinephrine mediates facultative carbohydrate-induced thermogenesis in human skeletal muscle. Am J Physiol 1989; 257: E340–5Astrup, A Simonsen, L Bulow, J Madsen, J Christensen, NJ
Aksnes AK, Brundin T, Hjeltnes N, Wahren J: Metabolic, thermal and circulatory effects of intravenous infusion of amino acids in tetraplegic patients. Clin Physiol 1995; 15: 377–96Aksnes, AK Brundin, T Hjeltnes, N Wahren, J
Shido O, Romanovsky AA, Ungar AL, Blatteis CM: Role of intrapreoptic norepinephrine in endotoxin-induced fever in guinea pigs. Am J Physiol 1993; 265: R1369–75Shido, O Romanovsky, AA Ungar, AL Blatteis, CM
Van Zoeren JG, Stricker EM: Thermal homeostasis in rats after intrahypothalamic injections of 6-hyroxydopamine. Am J Physiol 1976; 230: 932–9Van Zoeren, JG Stricker, EM
Girod V, Bouvier M, Grelot L: Characterization of lipopolysaccharide-induced emesis in conscious piglets: Effects of cervical vagotomy, cyclooxygenase inhibitors and a 5-HT(3) receptor antagonist. Neuropharmacology 2000; 39: 2329–35Girod, V Bouvier, M Grelot, L
Hansen MK, Krueger JM: Subdiaphragmatic vagotomy blocks the sleep- and fever-promoting effects of interleukin-1beta. Am J Physiol 1997; 273: R1246–53Hansen, MK Krueger, JM
Blatteis CM, Sehic E, Li S: Pyrogen sensing and signaling: Old views and new concepts. Clin Infect Dis 2000; 31( suppl 5): S168–77Blatteis, CM Sehic, E Li, S
Lopez M, Sessler DI, Walter K, Emerick T, Ayyalapu A: Reduced sweating threshold during exercise-induced hyperthermia. Pflugers Arch 1995; 430: 606–11Lopez, M Sessler, DI Walter, K Emerick, T Ayyalapu, A
Tayefeh F, Plattner O, Sessler DI, Ikeda T, Marder D: Circadian changes in the sweating-to-vasoconstriction interthreshold range. Pflugers Arch 1998; 435: 402–6Tayefeh, F Plattner, O Sessler, DI Ikeda, T Marder, D
Hessemer V, Brück K: Influence of menstrual cycle on thermoregulatory, metabolic, and heart rate responses to exercise at night. J Appl Physiol 1985; 59: 1911–7Hessemer, V Brück, K
Fig. 1. Sweating rate on chest (SRch; top  ) or forearm cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 1. Sweating rate on chest (SRch; top 
	) or forearm cutaneous vascular conductance (CVC; bottom 
	) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 1. Sweating rate on chest (SRch; top  ) or forearm cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during heating. Amino acid infusion significantly increased the threshold for sweating and cutaneous vasodilation. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
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Fig. 2. Oxygen consumption (V̇o2; top  ) or fingertip cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 2. Oxygen consumption (V̇o2; top 
	) or fingertip cutaneous vascular conductance (CVC; bottom 
	) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
Fig. 2. Oxygen consumption (V̇o2; top  ) or fingertip cutaneous vascular conductance (CVC; bottom  ) as a function of calculated core temperature (Tc) during cooling. Amino acid infusion significantly increased the threshold for thermogenesis and cutaneous vasoconstriction. Values are plotted at 1-min intervals and shown as mean ± SD for nine men.
×
Table 1. Baseline Values (before Saline or Amino Acid Infusion)
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Table 1. Baseline Values (before Saline or Amino Acid Infusion)
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Table 2. Plasma Amino Acid Concentrations (nM/ml)
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Table 2. Plasma Amino Acid Concentrations (nM/ml)
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Table 3. Mean Skin Temperatures, Core Temperatures, Calculated Thresholds, and Gains
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Table 3. Mean Skin Temperatures, Core Temperatures, Calculated Thresholds, and Gains
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