ライフサイエンスコーパス: heat production

1 y, followed by heat loss exceeding metabolic heat production.

2 ile cycling of SERCA, contributing to muscle heat production.

3 te (500 W) or high (700 W) rate of metabolic heat production.

4 inct changes in gut microbiota and increased heat production.

5 lative to moderate (400 W) rate of metabolic heat production.

6 s uncoupling of the SERCA pump and increased heat production.

7 ing that Sln is the basis for Serca-mediated heat production.

8 uman carotid artery samples showed increased heat production.

9 f surface heat loss and declining radiogenic heat production.

10 reliable surrogate measure of UCP1-mediated heat production.

11 elivery of nutrients to brown adipocytes for heat production.

12 te (ATP) production but energy efficient for heat production.

13 when active stimulate heat loss and inhibit heat production.

14 the body, and when active, may contribute to heat production.

15 ore fat while that of BAT is to burn fat for heat production.

16 a complex multi-organ metabolic response for heat production.

17 causes a hypermetabolic state with increased heat production.

18 ters may be due to the absence of endogenous heat production.

19 ing than hamsters, due in part to endogenous heat production.

20 brain mitochondrial uncoupling activity and heat production.

21 ion, kinetics, and quantity of intracellular heat production.

22 hanges in food intake, fat malabsorption, or heat production, although intestinal lipid secretion kin

23 monstrated a 42 +/- 7 % decrease in cortical heat production and a 35 +/- 10 % reduction in oxygen co

24 and beige adipose tissue is specialized for heat production and can be activated to reduce obesity a

25 allometric models, the relationship between heat production and cell carbon content or surface area

26 effects of methylone and MDPV on intra-brain heat production and cutaneous vascular tone, two critica

27 Irisin deficiency reduced heat production and decreased the expression of uncoupli

28 rylation from respiration, thereby promoting heat production and decreasing oxyradical production.

29 n adipose tissue (BAT)-long known to promote heat production and energy expenditure in infants and hi

30 highly activated mitochondria and increased heat production and energy expenditure.

31 hysiological mechanisms (i.e., intracerebral heat production and heat loss via skin surfaces) that un

32 ature is regulated by balancing the rates of heat production and heat loss.

33 pothermia, mediated by reciprocal changes in heat production and loss, as well as dramatic cold-seeki

34 was determined by calculation of both brain heat production and oxygen consumption.

35 Heat production and RMR were significantly elevated for

36 Heat production and sweat rate were not different during

37 egrees C causes large decreases in metabolic heat production and wing-beat frequency in honeybees dur

38 ral selectivity, low power requirements, low heat production, and fast release times, along with the

39 This excitatory mechanism of heat production appears to be activated on demand, durin

40 proved methods for the direct measurement of heat production as the signature function of brown adipo

41 ocricetus auratus) do not exhibit endogenous heat production before 3 weeks of age and do not huddle

42 latation during moderate (400 W of metabolic heat production) but not high (700 W of metabolic heat p

43 Fundamental rheology, yeasts heat production by isothermal microcalorimetry and the i

44 At the end of the series, recovery heat production by UCP-3tg fibres, 1.575 +/- 0.246 relat

45 the increase of the volume and the metabolic heat production by yeast.

46 Cortical heat production, calculated as the product of CBF, the t

47 renergic agonist known to activate metabolic heat production, CL316,243, was employed to evaluate whe

48 ive of a direct regulatory role for Them2 in heat production, cultured primary brown adipocytes from

49 Cortical heat production decreased by 78 +/- 6 % while oxygen use

50 nown to play an important role in regulating heat production during cold exposure, the biological fun

51 On the day of heat production, electron-translucent pockets are subseq

52 and severe cold adaptation and that loss of heat production from one thermogenic pathway leads to in

53 ances of K, Th, and U indicate that internal heat production has declined substantially since Mercury

54 The balance between metabolic heat production, heat removal by blood flow, and heat co

55 Human obesity is associated with increased heat production; however, subcutaneous adipose tissue pr

56 l metabolic rate in the fetal sheep based on heat production in a local region of the brain.

57 ) and beige adipose tissue combust fuels for heat production in adult humans, and so constitute an ap

58 Although the exact mechanisms of local heat production in brain tissue remain to be confirmed,

59 regulators of mitochondrial respiration and heat production in brown adipocytes are the transcriptio

60 was assumed to be a key event for triggering heat production in brown fat.

61 ter in isothermal mode, we directly measured heat production in eukaryotic protists from 5 phyla span

62 constraint leading to a universally constant heat production in single-celled eukaryotes is related t

63 2+) ATPase (SERCA) pump, could contribute to heat production in skeletal muscle.

64 We conclude that local measurements of heat production in the brain provide a useful index of o

65 ssue (BAT), the major source of nonshivering heat production in the rat.

66 ) mice show increased oxygen consumption and heat production, indicating that they expend more energy

67 production) but not high (700 W of metabolic heat production) intensity exercise bouts performed in t

68 on) relative to moderate (500 W of metabolic heat production) intensity exercise.

69 , and the relationship between body size and heat production investigated.

70 ize, body fatness, pregnancy weight gain and heat production is predicted to influence maternal therm

71 Heat production is stimulated by the sympathetic nervous

72 32.5 degrees C), pups at both ages increased heat production, maintained an elevated interscapular te

73 Thus, variation in heat production may be the primary mechanism for achievi

74 F-FDG accumulation in BAT by 3 stressors and heat production measured in vivo by thermal imaging.

75 Since brain metabolism is accompanied by heat production, measurement of brain temperature offers

76 Our results reveal that metabolic heat production normalized to cell mass is virtually con

77 at uses Monte Carlo simulation, based on the heat production of major seed storage compounds to unrav

78 pancy between the observed heat flux and the heat production of the mid-ocean ridge basalt source reg

79 a resulted in no significant change in brain heat production or oxygen consumption, suggesting the ad

80 ysiological processes such as ATP synthesis, heat production, or regulation of the reactive oxygen sp

81 That heat production per unit cell surface area is constant s

82 ygen species during high (700 W of metabolic heat production) relative to moderate (500 W of metaboli

83 Prior to heat production, the rER- and plasma-membrane pockets ar

84 Heat production (thermogenesis) in brown adipose tissue

85 ing with the stress of chronically increased heat production through exercise.

86 he requirement for unusually high radiogenic heat production to achieve crustal melting temperatures.

87 delivery of a PTH2R antagonist had impaired heat production upon cold exposure, but no change in bas

88 Heat production was compared to oxygen use in 20 near-te

89 Heat production was partitioned into initial heat (due t

90 Initial heat production was similar for the UCP-3tg and wild-typ

91 xpression and maximal norepinephrine-induced heat production were gradually increased during cold-acc

92 Force and heat production were measured during a series of thirty

93 calorimetry, T3 and TSH increased follicular heat production, whereas T3/T4 and TRH stimulated ATP pr

94 ice exhibited increased O(2) consumption and heat production, which were accompanied by increased rat

95 t extremely difficult to balance terrestrial heat production with the observed heat flow.