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Human Body Exergy Metabolism

Yıl 2013, Cilt: 16 Sayı: 2, 73 - 80, 01.06.2013

Öz

The exergy analysis of the human body is a tool that can provide indicators of health and life quality. To perform the exergy balance it is necessary to calculate the metabolism on an exergy basis, or metabolic exergy, although there is not yet consensus in its calculation procedure. Hence, the aim of this work is to provide a general method to evaluate this physical quantity for human body based on indirect calorimetry data. To calculate the metabolism on an exergy basis it is necessary to define the reference reactions and obtain their exergy variation. The reference reactions of the energy substrates are represented by the oxidation of the glucose, palmitic acid and a representative amino acid. Hence, from the exergy variation of these reactions and the consumption rate of the substrates, the metabolic exergy is determined. Results, for basal conditions and during physical activities, indicate that the difference between exergy and energy metabolisms is lower than 5%. Moreover, the body converts approximately 60% of the exergy of nutrients into available exergy to perform work.

Kaynakça

  • Glucose Palmitic Ac. Amino Ac. Hayne (2008) ‒16506 ‒39141 ‒18964
  • Cortassa (2002) ‒16516 ‒39223 ‒17578
  • Finally, the metabolisms on energy and exergy basis using the data from Hayne (2008) and from Cortassa et al.
  • (2002) are 2 2 11371 2366 6891 Hayne O CO N
  • M m m m    (18) , 2 2 9501 3963 6979 M Hayne O CO N
  • B m m m    (19) 2 2 11179 2502 1580 Cortassa O CO N
  • M m m m    (20) , 2 2 9558 3928 1823 M Cortassa O CO N
  • B m m m    (21) 2 Energy and exergy metabolism 1 Basal conditions Results in Table 5 indicate the metabolism on energy and exergy basis, considering the oxidation of proteins (M and B M ) and disregarding the oxidation of proteins (M p and B Mp ) for the energy measurements obtained by Hardy & Du Bois (1938). For this condition, the authors obtained that the metabolism is 79.8W. In all cases the difference between this value and the ones calculated herein was not larger than 2%. Furthermore, the difference of the metabolism using the two different references of thermodynamic properties did not differ more than 2%. The ratio of metabolism on energy and exergy basis
  • (considering and disregarding the oxidation of proteins) did not exceed 1.02. Hence, as in Batato et al. (1990), the approximation B M ≈ M for basal conditions is valid.
  • Table 5. Metabolism in energy and exergy basis with the oxidation of amino acids (M and B M ) and without the oxidation of amino acids (M p and B Mp ). Hayne (2008) (W) Cortassa et al. (2002) (W) M 3 9 M p 3 1 B M 8 7 B Mp 9 0 2 Physical activities For the experimental results of Figure 2 the metabolism in energy and exergy basis was calculated, using the values of thermodynamic properties of Cortassa et al. (2002) indicated in Eqs. (20) and (21), due to the small difference between results in Table 5. Figure 3 indicates M, B M and B QM for the experimental data of Figure 2. The difference of B M and B QM is one order of magnitude, indicating that when the metabolism is calculated as B QM (taking into account only the thermal exergy), more than 95% of the exergy content of metabolism is disregarded. Therefore, most of the available exergy to perform work would be disregarded. In Figure 4 it is demonstrated the ratio of the metabolism on energy and exergy basis as a function of time. In the first five minutes, the ratio B M /M ranged from 04 to 1.01 (time when the subject controlled the Figure 5. Ratio of the metabolism considering and disregarding the oxidation of proteins during the treadmill test.
  • Figure 6 Result of B M , W MAX and B QM as a function of time during the treadmill test. The first two properties are indicated in the left axis, the last on in the right side axis. Table 6 indicates the metabolism on exergy basis, the maximum available work, the exergy rate associated with metabolism (B QM ) and the ratio B M /M. It is possible to note that the thermal portion of metabolism is approximately 5% of exergy metabolism and the maximum available work from ATP hydrolysis corresponds to 60% of exergy metabolism. Hence, for the 11 runners more than 95% of the exergy released from the oxidation of nutrients would be neglected if B QM be considered as the exergy source of the body, whereas in fact the body uses 60% of the exergy content of nutrients. The ratio of metabolism in energy and exergy basis ranged from 1.01 to 1.03, indicating that the approximation B M ≈M is valid for physical activities. Conclusions In this work analyses of the human metabolism on energy and exergy basis were performed and it was proposed a method and an equation to calculate the metabolic exergy. From the range of tests analyzed it was possible to conclude that: ▪ For basal conditions results the metabolism on energy and exergy basis did not differ more than 2%, for the different thermodynamic properties. For basal conditions, results obtained from Batato et al. (1990) were verified; ▪
  • For the treadmill running tests, the metabolism on energy and exergy basis are very close. The ratio is equal to 05 in only one point; in the rest of the test the ratio was lower. ▪ Finally, the contribution of proteins did not exceed 3% of the total metabolism (energy and exergy basis) during physical activities and in basal conditions. Hence, the oxidation of proteins may be disregarded in a healthy person in basal conditions and under physical activities. ▪ The exergy released in ATP hydrolysis is the maximum available work that the body can obtain from the oxidation of energy substrates. Hence, the body keeps approximately 60% of the exergy content of nutrients in the chemical bounds of ATP. Acknowledgments: The authors acknowledge FAPESP (São Paulo Research Foundation) for his PhD grant 09/17578‒0 and CNPq (National Research Council) for grant 306033/2017-7. The authors also acknowledge the Sports medicine group and FIFA Medical Center of Institute of Orthopedics and Traumatology of the University of São Paulo Medical School. Nomenclature: ADP adenosine diphosphate ATP adenosine triphosphate b specific exergy, J/kg B body exergy, J B exergy rate and flow rate, W g specific free energy, J/kg G
  • Gibbs free energy rate, W h specific enthalpy, J/kg H enthalpy flow rate, W M metabolism, W m mass flow rate, kg/s Table Integration for 11 runners of metabolism in energy basis, metabolism in exergy basis, maximum available work, exergy rate associated with metabolism and ratio of metabolism on energy and exergy basis. Subject Time M (kJ/kg) B M (kJ/kg) W MAX (kJ/kg) B QM (kJ/kg) B M /M 1 0 16851 17307 10651 439 03 2 0 17617 17897 10911 457 02 3 0 15729 16150 9916 383 03 4 0 17026 17308 10585 437 02 5 0 27088 27712 17091 843 02 6 0 30434 30951 18990 880 02 7 0 25312 26019 16086 617 03 8 0 29907 30351 18586 868 01 9 0 22699 23037 14100 796 01 10 0 20826 21343 13165 702 02 11 0 42545 43504 26825 1174 02 P i phosphate group
  • Q heat transfer rate, W RQ respiratory quotient, ‒ T temperature, K t time, min V velocity, m/s W work, W Greek symbols η exergy efficiency, % ϕ relative humidity, % Subscripts and superscripts reference ami amino acids ATP adenosine triphosphate b body c convective carb carbohydrates dest destruction e evaporative ex expired in inspired lip lipids M metabolic MAX maximum oxi complete oxidation p disregarding proteins r radiative res respiration References: Alberty, R. A. (1998). Calculation of standard transformed gibbs energies and standard transformed enthalpies of biochemical reactants. Archives of biochemistry and biophysics, 353, 16–130.
  • Alberty, R. A., Goldeberg, R. N. (1992). Standard thermodynamic formation properties for the adenosine 5’-triphosphate series. Biochemistry. ACS Publications, 31, 10610–10615.
  • Handbook ASHRAE (2009). Fundamentals. American Society of Heating, Refrigerating and Air-Conditioning Engineers, Inc., Atlanta GA.
  • Aoki, I. (1991). Entropy principle for human development, growth and aging. Journal of Theoretical Biology, 150, 215-2
  • Balmer, R. T. (1984). Entropy and aging in biological systems. Chemical Engineering Communications, 17, 171-1
  • Batato, M., Borel, L., Deriaz, O., Jequier, E. (1990). Analyse exergétique théorique et expérimentale du corps humain. Entropie, 26, 120-130.
  • Coratassa, S., Aon, M. A., Iglesias, A. A., Lloyd, D. (2002). An introduction to metabolic and cellular engineering. London: World Scientific Pub Co Inc.
  • Diener, J. R. C. (1997). Indirect calorimetry (in Portuguese). AMB Revista da Associação Médica Brasileira, 43, 245–253.
  • Doran, M. D. (1995). Bioprocess Engineering Principles. Cambridge, UK: Cambridge University Press.
Yıl 2013, Cilt: 16 Sayı: 2, 73 - 80, 01.06.2013

Öz

Kaynakça

  • Glucose Palmitic Ac. Amino Ac. Hayne (2008) ‒16506 ‒39141 ‒18964
  • Cortassa (2002) ‒16516 ‒39223 ‒17578
  • Finally, the metabolisms on energy and exergy basis using the data from Hayne (2008) and from Cortassa et al.
  • (2002) are 2 2 11371 2366 6891 Hayne O CO N
  • M m m m    (18) , 2 2 9501 3963 6979 M Hayne O CO N
  • B m m m    (19) 2 2 11179 2502 1580 Cortassa O CO N
  • M m m m    (20) , 2 2 9558 3928 1823 M Cortassa O CO N
  • B m m m    (21) 2 Energy and exergy metabolism 1 Basal conditions Results in Table 5 indicate the metabolism on energy and exergy basis, considering the oxidation of proteins (M and B M ) and disregarding the oxidation of proteins (M p and B Mp ) for the energy measurements obtained by Hardy & Du Bois (1938). For this condition, the authors obtained that the metabolism is 79.8W. In all cases the difference between this value and the ones calculated herein was not larger than 2%. Furthermore, the difference of the metabolism using the two different references of thermodynamic properties did not differ more than 2%. The ratio of metabolism on energy and exergy basis
  • (considering and disregarding the oxidation of proteins) did not exceed 1.02. Hence, as in Batato et al. (1990), the approximation B M ≈ M for basal conditions is valid.
  • Table 5. Metabolism in energy and exergy basis with the oxidation of amino acids (M and B M ) and without the oxidation of amino acids (M p and B Mp ). Hayne (2008) (W) Cortassa et al. (2002) (W) M 3 9 M p 3 1 B M 8 7 B Mp 9 0 2 Physical activities For the experimental results of Figure 2 the metabolism in energy and exergy basis was calculated, using the values of thermodynamic properties of Cortassa et al. (2002) indicated in Eqs. (20) and (21), due to the small difference between results in Table 5. Figure 3 indicates M, B M and B QM for the experimental data of Figure 2. The difference of B M and B QM is one order of magnitude, indicating that when the metabolism is calculated as B QM (taking into account only the thermal exergy), more than 95% of the exergy content of metabolism is disregarded. Therefore, most of the available exergy to perform work would be disregarded. In Figure 4 it is demonstrated the ratio of the metabolism on energy and exergy basis as a function of time. In the first five minutes, the ratio B M /M ranged from 04 to 1.01 (time when the subject controlled the Figure 5. Ratio of the metabolism considering and disregarding the oxidation of proteins during the treadmill test.
  • Figure 6 Result of B M , W MAX and B QM as a function of time during the treadmill test. The first two properties are indicated in the left axis, the last on in the right side axis. Table 6 indicates the metabolism on exergy basis, the maximum available work, the exergy rate associated with metabolism (B QM ) and the ratio B M /M. It is possible to note that the thermal portion of metabolism is approximately 5% of exergy metabolism and the maximum available work from ATP hydrolysis corresponds to 60% of exergy metabolism. Hence, for the 11 runners more than 95% of the exergy released from the oxidation of nutrients would be neglected if B QM be considered as the exergy source of the body, whereas in fact the body uses 60% of the exergy content of nutrients. The ratio of metabolism in energy and exergy basis ranged from 1.01 to 1.03, indicating that the approximation B M ≈M is valid for physical activities. Conclusions In this work analyses of the human metabolism on energy and exergy basis were performed and it was proposed a method and an equation to calculate the metabolic exergy. From the range of tests analyzed it was possible to conclude that: ▪ For basal conditions results the metabolism on energy and exergy basis did not differ more than 2%, for the different thermodynamic properties. For basal conditions, results obtained from Batato et al. (1990) were verified; ▪
  • For the treadmill running tests, the metabolism on energy and exergy basis are very close. The ratio is equal to 05 in only one point; in the rest of the test the ratio was lower. ▪ Finally, the contribution of proteins did not exceed 3% of the total metabolism (energy and exergy basis) during physical activities and in basal conditions. Hence, the oxidation of proteins may be disregarded in a healthy person in basal conditions and under physical activities. ▪ The exergy released in ATP hydrolysis is the maximum available work that the body can obtain from the oxidation of energy substrates. Hence, the body keeps approximately 60% of the exergy content of nutrients in the chemical bounds of ATP. Acknowledgments: The authors acknowledge FAPESP (São Paulo Research Foundation) for his PhD grant 09/17578‒0 and CNPq (National Research Council) for grant 306033/2017-7. The authors also acknowledge the Sports medicine group and FIFA Medical Center of Institute of Orthopedics and Traumatology of the University of São Paulo Medical School. Nomenclature: ADP adenosine diphosphate ATP adenosine triphosphate b specific exergy, J/kg B body exergy, J B exergy rate and flow rate, W g specific free energy, J/kg G
  • Gibbs free energy rate, W h specific enthalpy, J/kg H enthalpy flow rate, W M metabolism, W m mass flow rate, kg/s Table Integration for 11 runners of metabolism in energy basis, metabolism in exergy basis, maximum available work, exergy rate associated with metabolism and ratio of metabolism on energy and exergy basis. Subject Time M (kJ/kg) B M (kJ/kg) W MAX (kJ/kg) B QM (kJ/kg) B M /M 1 0 16851 17307 10651 439 03 2 0 17617 17897 10911 457 02 3 0 15729 16150 9916 383 03 4 0 17026 17308 10585 437 02 5 0 27088 27712 17091 843 02 6 0 30434 30951 18990 880 02 7 0 25312 26019 16086 617 03 8 0 29907 30351 18586 868 01 9 0 22699 23037 14100 796 01 10 0 20826 21343 13165 702 02 11 0 42545 43504 26825 1174 02 P i phosphate group
  • Q heat transfer rate, W RQ respiratory quotient, ‒ T temperature, K t time, min V velocity, m/s W work, W Greek symbols η exergy efficiency, % ϕ relative humidity, % Subscripts and superscripts reference ami amino acids ATP adenosine triphosphate b body c convective carb carbohydrates dest destruction e evaporative ex expired in inspired lip lipids M metabolic MAX maximum oxi complete oxidation p disregarding proteins r radiative res respiration References: Alberty, R. A. (1998). Calculation of standard transformed gibbs energies and standard transformed enthalpies of biochemical reactants. Archives of biochemistry and biophysics, 353, 16–130.
  • Alberty, R. A., Goldeberg, R. N. (1992). Standard thermodynamic formation properties for the adenosine 5’-triphosphate series. Biochemistry. ACS Publications, 31, 10610–10615.
  • Handbook ASHRAE (2009). Fundamentals. American Society of Heating, Refrigerating and Air-Conditioning Engineers, Inc., Atlanta GA.
  • Aoki, I. (1991). Entropy principle for human development, growth and aging. Journal of Theoretical Biology, 150, 215-2
  • Balmer, R. T. (1984). Entropy and aging in biological systems. Chemical Engineering Communications, 17, 171-1
  • Batato, M., Borel, L., Deriaz, O., Jequier, E. (1990). Analyse exergétique théorique et expérimentale du corps humain. Entropie, 26, 120-130.
  • Coratassa, S., Aon, M. A., Iglesias, A. A., Lloyd, D. (2002). An introduction to metabolic and cellular engineering. London: World Scientific Pub Co Inc.
  • Diener, J. R. C. (1997). Indirect calorimetry (in Portuguese). AMB Revista da Associação Médica Brasileira, 43, 245–253.
  • Doran, M. D. (1995). Bioprocess Engineering Principles. Cambridge, UK: Cambridge University Press.
Toplam 22 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Invited ECOS 2012 Papers
Yazarlar

Carlos Mady

Yayımlanma Tarihi 1 Haziran 2013
Yayımlandığı Sayı Yıl 2013 Cilt: 16 Sayı: 2

Kaynak Göster

APA Mady, C. (2013). Human Body Exergy Metabolism. International Journal of Thermodynamics, 16(2), 73-80.
AMA Mady C. Human Body Exergy Metabolism. International Journal of Thermodynamics. Haziran 2013;16(2):73-80.
Chicago Mady, Carlos. “Human Body Exergy Metabolism”. International Journal of Thermodynamics 16, sy. 2 (Haziran 2013): 73-80.
EndNote Mady C (01 Haziran 2013) Human Body Exergy Metabolism. International Journal of Thermodynamics 16 2 73–80.
IEEE C. Mady, “Human Body Exergy Metabolism”, International Journal of Thermodynamics, c. 16, sy. 2, ss. 73–80, 2013.
ISNAD Mady, Carlos. “Human Body Exergy Metabolism”. International Journal of Thermodynamics 16/2 (Haziran 2013), 73-80.
JAMA Mady C. Human Body Exergy Metabolism. International Journal of Thermodynamics. 2013;16:73–80.
MLA Mady, Carlos. “Human Body Exergy Metabolism”. International Journal of Thermodynamics, c. 16, sy. 2, 2013, ss. 73-80.
Vancouver Mady C. Human Body Exergy Metabolism. International Journal of Thermodynamics. 2013;16(2):73-80.