ライフサイエンスコーパス: heat production

1 vere (hibernation) curtailments to metabolic heat production.

2 roach, existing wells can support low-carbon heat production.

3 ysis, instead shifting toward glucose-driven heat production.

4 inct changes in gut microbiota and increased heat production.

5 of 1-10 megapascal stress drops and limited heat production.

6 ips among muscle mechanics, biochemistry and heat production.

7 rolling the rate of heat loss and consequent heat production.

8 predictable ratios that can be compared with heat production.

9 reliable surrogate measure of UCP1-mediated heat production.

10 ch can then be utilized for ATP synthesis or heat production.

11 by increasing their metabolism, resulting in heat production.

12 which is possibly associated with increased heat production.

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

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

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

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

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

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

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

20 uman carotid artery samples showed increased heat production.

21 f surface heat loss and declining radiogenic heat production.

22 elivery of nutrients to brown adipocytes for heat production.

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

24 when active stimulate heat loss and inhibit heat production.

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

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

27 causes a hypermetabolic state with increased heat production.

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

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

30 brain mitochondrial uncoupling activity and heat production.

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

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

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

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

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

36 ouse and human, to test their recruitment to heat production and conservation We found that insulatin

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

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

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

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

41 respiration from ATP synthesis and promotes heat production and energy expenditure.

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

43 nt core body temperature (T(b)) by balancing heat production and heat dissipation.

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

45 eladus' ocean depends on the balance between heat production and heat loss.

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

47 al and describe the underlying mechanisms of heat production and infrared detection.

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

49 ion potentials respectively, suggesting that heat production and membrane deformation associated with

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

51 Heat production and RMR were significantly elevated for

52 heat stress due to their intensive metabolic heat production and small surface:volume ratio.

53 Heat production and sweat rate were not different during

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

55 a vasoconstrictor known to mediate brown fat heat production, and by CL 316,243, a specific beta(3)-a

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

57 cess that contributes to energy expenditure, heat production, and various lipid signaling pathways.

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

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

60 Here we show that 30 years of geothermal heat production at Coso depleted shear stresses within t

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

62 nvestigate how salinity and the partition of heat production between the silicate core and the ice sh

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

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

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

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

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

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

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

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

71 However, even with reductions in metabolic heat production, desiccation likely limits foraging at t

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

73 t muscle NST may be the primary mechanism of heat production during cold stress in large mammals lack

74 ygen consumption, uncoupled respiration, and heat production during cold- and diet-induced thermogene

75 squirrels have delayed when they up-regulate heat production during torpor to prevent freezing.

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

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

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

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

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

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

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

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

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

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

86 ary gland fat pads are actively recruited to heat production In contrast, the body-wide adipose depot

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

88 consumption, respiratory exchange ratio, and heat production in male offspring.

89 notypic variation across the phylogeny, with heat production in multiple clades reaching up to 15 deg

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

91 2+) ATPase (SERCA) pump, could contribute to heat production in skeletal muscle.

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

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

94 erature perception, non-renal water loss and heat production in the recent adaptation of North Africa

95 mediated by increased heat loss, but not by heat production, in SHR.

96 ion of non-movement-related factors, such as heat production, increases.

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

98 pation effects come out as a core reason for heat production instead of molecular conduction.

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

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

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

102 Nevertheless, mitochondrial heat production is crucial for the maintenance of body t

103 Radiogenic heat production is fundamental to the energy budget of p

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

105 e thermoneutral zone, below which additional heat production is required to defend core body temperat

106 Heat production is stimulated by the sympathetic nervous

107 32.5 degrees C), pups at both ages increased heat production, maintained an elevated interscapular te

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

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

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

111 tissue (BAT) is a fat tissue specialized in heat production (non-shivering thermogenesis) and used b

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

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

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

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

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

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

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

119 unidentified constraint for models of tidal heat production, shell thickness, and the long-term evol

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

121 Heat production (thermogenesis) in brown adipose tissue

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

123 anges in BAT gene expression consistent with heat production through increased peroxisomal lipid oxid

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

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

126 ticularly to increase energy expenditure and heat production upon cold exposure.

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

128 xposure over the first 5 days of life, total heat production was improved while shivering intensity d

129 ory of the Earth when the rate of radiogenic heat production was on average twice the present-day rat

130 Heat production was partitioned into initial heat (due t

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

132 ies of skin offset the total requirement for heat production We hypothesize that the adipose componen

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

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

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

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

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

138 ive technique to study single cell metabolic heat production without altering the cell behavior, but