PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 23214269-6 2012 Corticosteroid binding globulin (CBG) concentration differ significantly between high and low tolerant groups of rats resulting in significant changes in circulating free corticosterone that in turn may be responsible for individual differences in hypoxic gasping time. Corticosterone 171-185 serpin family A member 6 Rattus norvegicus 0-31 23214269-6 2012 Corticosteroid binding globulin (CBG) concentration differ significantly between high and low tolerant groups of rats resulting in significant changes in circulating free corticosterone that in turn may be responsible for individual differences in hypoxic gasping time. Corticosterone 171-185 serpin family A member 6 Rattus norvegicus 33-36 21828178-8 2011 Thus, the increase in circulating CBG levels after stress restrains the rise in free corticosterone concentrations for approximately 20 min in the face of mounting total hormone levels in the circulation. Corticosterone 85-99 serpin family A member 6 Rattus norvegicus 34-37 19833863-2 2010 Corticosterone takes part in the mechanisms that govern development, and its effects are regulated in particular by corticosterone-binding globulin (CBG) and glucocorticoid receptor (GR). Corticosterone 0-14 serpin family A member 6 Rattus norvegicus 149-152 19833863-2 2010 Corticosterone takes part in the mechanisms that govern development, and its effects are regulated in particular by corticosterone-binding globulin (CBG) and glucocorticoid receptor (GR). Corticosterone 116-130 serpin family A member 6 Rattus norvegicus 149-152 10223280-6 1999 gain, plasma transcortin and thymus weight were reduced to a greater extent by chronic corticosterone in BN rats than in F344 rats, possibly as a consequence of higher free, active fraction of plasma corticosterone due to lower plasma transcortin concentrations and/or a greater efficiency of GR-related mechanisms in BN rats. Corticosterone 87-101 serpin family A member 6 Rattus norvegicus 13-24 18817795-5 2009 The present study investigated whether the levels of circulating corticosterone and its binding protein, corticosteroid binding globulin (CBG), are altered with reproductive experience and pup-exposure during late pregnancy and the postpartum. Corticosterone 65-79 serpin family A member 6 Rattus norvegicus 105-136 18817795-5 2009 The present study investigated whether the levels of circulating corticosterone and its binding protein, corticosteroid binding globulin (CBG), are altered with reproductive experience and pup-exposure during late pregnancy and the postpartum. Corticosterone 65-79 serpin family A member 6 Rattus norvegicus 138-141 18817795-10 2009 Corticosterone and CBG levels were positively correlated with specific maternal behaviors during the first week postpartum in parturient rats, but not in sensitized rats, suggesting a role for corticosterone in the modulation of maternal behavior in parturient rats alone. Corticosterone 193-207 serpin family A member 6 Rattus norvegicus 19-22 11849373-9 2002 These data suggest that in PM rats, an elevation of basal concentrations of corticosterone, in face of reduced CBG and probably increased hippocampal MR lead to a much larger impact of corticosterone on target cells that mediate the negative-feedback mechanism on the activities of both the HPA axis and sympathoadrenal one. Corticosterone 76-90 serpin family A member 6 Rattus norvegicus 111-114 10810451-5 2000 Kd and Bmax values of 0.646 and 578 nM for corticosterone binding to rat CBG and 0.577 and 19.8 nM for cortisol binding to sheep CBG, respectively, were measured. Corticosterone 43-57 serpin family A member 6 Rattus norvegicus 73-76 15994759-8 2005 RESULTS: Basal plasma corticosterone and corticosterone binding globulin (CBG) concentrations were significantly increased in short- and long-term hyperthyroid rats, and by 60 days, cerebrospinal fluid (CSF) corticosterone levels were significantly increased. Corticosterone 41-55 serpin family A member 6 Rattus norvegicus 74-77 15128271-8 2004 This testosterone-dependent decrease in pituitary transcortin was associated, in vitro, with an enhanced nuclear uptake of corticosterone. Corticosterone 123-137 serpin family A member 6 Rattus norvegicus 50-61 11507677-8 2001 Fatty acids may increase the affinity of CBG for corticosterone, which would make WAT cells less accessible to circulating glucocorticoids. Corticosterone 49-63 serpin family A member 6 Rattus norvegicus 41-44 10223280-6 1999 gain, plasma transcortin and thymus weight were reduced to a greater extent by chronic corticosterone in BN rats than in F344 rats, possibly as a consequence of higher free, active fraction of plasma corticosterone due to lower plasma transcortin concentrations and/or a greater efficiency of GR-related mechanisms in BN rats. Corticosterone 87-101 serpin family A member 6 Rattus norvegicus 235-246 8319565-4 1993 This rise in FFA was associated with a 2- to 3-fold increase in the binding indices (C values; liters per g) of corticosterone (B) and progesterone to CBG 60-120 min postinjection (P < 0.001). Corticosterone 112-126 serpin family A member 6 Rattus norvegicus 151-154 9663647-9 1998 However, morphine did not significantly affect the weight of the liver, or the plasma CBG binding capacity for corticosterone, in rat pups. Corticosterone 111-125 serpin family A member 6 Rattus norvegicus 86-89 8932731-4 1996 These findings suggest that the reduced CBG levels might enhance the biological significance of existing glucocorticoid levels, beyond that assumed on the basis of plasma total corticosterone levels. Corticosterone 177-191 serpin family A member 6 Rattus norvegicus 40-43 8778907-10 1996 Instead, the differences in available receptor levels may have been a function of plasma corticosteroid binding globulin (CBG) levels which regulate free corticosterone levels. Corticosterone 154-168 serpin family A member 6 Rattus norvegicus 89-120 8778907-10 1996 Instead, the differences in available receptor levels may have been a function of plasma corticosteroid binding globulin (CBG) levels which regulate free corticosterone levels. Corticosterone 154-168 serpin family A member 6 Rattus norvegicus 122-125 8404624-6 1993 Steroids that bound to CBG, e.g. corticosterone and cortisol, noncompetitively inhibited CBG"s binding to the receptor. Corticosterone 33-47 serpin family A member 6 Rattus norvegicus 23-26 8404624-6 1993 Steroids that bound to CBG, e.g. corticosterone and cortisol, noncompetitively inhibited CBG"s binding to the receptor. Corticosterone 33-47 serpin family A member 6 Rattus norvegicus 89-92 9316834-3 1997 Since CBG-bound hormone is thought to be physiologically inactive, changes in CBG levels could affect corticosterone action independently of hormone levels per se. Corticosterone 102-116 serpin family A member 6 Rattus norvegicus 78-81 9316834-11 1997 Furthermore, the increase in CBG resulting from chronic exposure to morphine might contribute to the perpetuation of drug use and to adverse effects of drug exposure by impairing normal functions of corticosterone. Corticosterone 199-213 serpin family A member 6 Rattus norvegicus 29-32 7822484-9 1995 The observed differences between strains in corticosteroid-binding globulin (CBG) levels in plasma, pituitary, and immune tissue may mediate the differential access of corticosterone to neural versus immune tissues. Corticosterone 168-182 serpin family A member 6 Rattus norvegicus 44-75 7822484-9 1995 The observed differences between strains in corticosteroid-binding globulin (CBG) levels in plasma, pituitary, and immune tissue may mediate the differential access of corticosterone to neural versus immune tissues. Corticosterone 168-182 serpin family A member 6 Rattus norvegicus 77-80 2069858-6 1991 [3H]corticosterone binding with disc electrophoresis, run at 2 degrees C, gave a single peak with approximately the same Rf value for rat serum, purified CBG, and adrenal incubate; at 22 degrees C peaks were only seen for rat serum or purified CBG. Corticosterone 4-18 serpin family A member 6 Rattus norvegicus 154-157 1917978-3 1991 The dissociation rate constants of BB CBG for cortisol (4.42 nM) and corticosterone (1.43 nM) are both about 50% higher than those associated with Wistar CBG, but no obvious difference in the steroid binding specificity of BB and Wistar CBGs was detected. Corticosterone 69-83 serpin family A member 6 Rattus norvegicus 38-41 2069858-6 1991 [3H]corticosterone binding with disc electrophoresis, run at 2 degrees C, gave a single peak with approximately the same Rf value for rat serum, purified CBG, and adrenal incubate; at 22 degrees C peaks were only seen for rat serum or purified CBG. Corticosterone 4-18 serpin family A member 6 Rattus norvegicus 244-247 2069858-9 1991 It is possible that the adrenal protein may be CBG that has been internalized, modified and released with corticosterone. Corticosterone 106-120 serpin family A member 6 Rattus norvegicus 47-50 1863673-1 1991 During chromatography of renal tissue cytosolic proteins on DEAE-cellulose the protein specifically binding [3H]corticosterone is eluted within the potassium phosphate concentration range of 0.08-0.10 M. Analysis of kidney slices revealed the synthesis of [3H]transcortin whose electrophoretic mobility was close to that of the blood plasma protein. Corticosterone 112-126 serpin family A member 6 Rattus norvegicus 260-271 1997123-1 1991 The [3H]corticosterone-transcortin complexes from kidney cytosol show elution positions on DEAE-cellulose identical to serum transcortin. Corticosterone 8-22 serpin family A member 6 Rattus norvegicus 23-34 1997123-1 1991 The [3H]corticosterone-transcortin complexes from kidney cytosol show elution positions on DEAE-cellulose identical to serum transcortin. Corticosterone 8-22 serpin family A member 6 Rattus norvegicus 125-136 2238157-2 1990 The differences in the Schtern Folmer constants and the dissociation constants for the transcortin-corticosterone complex obtained during the protein titration by corticosterone may be due to different tryptophanyl surroundings in the molecules of the studied proteins. Corticosterone 99-113 serpin family A member 6 Rattus norvegicus 87-98 2238157-2 1990 The differences in the Schtern Folmer constants and the dissociation constants for the transcortin-corticosterone complex obtained during the protein titration by corticosterone may be due to different tryptophanyl surroundings in the molecules of the studied proteins. Corticosterone 163-177 serpin family A member 6 Rattus norvegicus 87-98 2305602-9 1990 Our results suggest that the maternal response of corticosteroid binding globulin to adrenalectomy depends on the pregnancy stage inasmuch as it may be influenced by a supply of corticosterone from the fetus during late pregnancy. Corticosterone 178-192 serpin family A member 6 Rattus norvegicus 50-81 2830101-0 1987 The influence of transcortin on adrenocorticotropin-stimulated corticosterone production in monolayer cultured rat adrenal cells. Corticosterone 63-77 serpin family A member 6 Rattus norvegicus 17-28 2594422-2 1989 Analgin and aminopyrine in doses of 10(-2) and 10(-3) increase the specific binding of labelled corticosterone by type-III glucocorticoid receptors of the hepatic cytosol and by blood plasma transcortin in modelled experiments. Corticosterone 96-110 serpin family A member 6 Rattus norvegicus 191-202 2497651-5 1989 These data demonstrate that physiological levels of corticosterone (40% pellet) restore vascular responsiveness, body weight, thymus weight, and transcortin levels to normal in ADRX rats, whereas higher levels (80% pellet) are necessary for restoration of the baroreflex. Corticosterone 52-66 serpin family A member 6 Rattus norvegicus 145-156 2741400-4 1989 At the same time, activation of glucose 6-phosphate dehydrogenase was accompanied by simultaneous alteration in content of transcortin-bound corticosterone in rat blood plasma. Corticosterone 141-155 serpin family A member 6 Rattus norvegicus 123-134 3205611-7 1988 As plasma concentrations of corticosteroid-binding globulin are known to increase markedly during this period, the t1/2 of protein-bound corticosterone was measured and that of free corticosterone was computed. Corticosterone 137-151 serpin family A member 6 Rattus norvegicus 28-59 3205611-11 1988 The increasing association of corticosterone with corticosteroid-binding globulin during this developmental period is the most likely explanation for the steep decline of volume of distribution and thus of the metabolic clearance rate for corticosterone. Corticosterone 30-44 serpin family A member 6 Rattus norvegicus 50-81 3205611-11 1988 The increasing association of corticosterone with corticosteroid-binding globulin during this developmental period is the most likely explanation for the steep decline of volume of distribution and thus of the metabolic clearance rate for corticosterone. Corticosterone 239-253 serpin family A member 6 Rattus norvegicus 50-81 34822681-5 2021 Levels of the high-specificity and -affinity corticosteroid-binding globulin protein increased in the lungs of both strains proportional to the rise in corticosterone levels following O3 exposure. Corticosterone 152-166 serpin family A member 6 Rattus norvegicus 45-76 2698528-5 1989 The equilibrium redistribution is revealed in the plasma between free corticosterone and corticosterone bound to transcortin at the different stages of the hypoxic exposure. Corticosterone 89-103 serpin family A member 6 Rattus norvegicus 113-124 3394170-0 1988 [Effect of transcortin on the corticosterone-transforming activity of cytosol from the rat liver]. Corticosterone 30-44 serpin family A member 6 Rattus norvegicus 11-22 3394170-3 1988 Under the influence of homogeneous transcortin samples, a decrease in the content of 5 beta-reduced corticosterone metabolites is revealed to occur depending on transcortin concentration in the system. Corticosterone 100-114 serpin family A member 6 Rattus norvegicus 35-46 3394170-3 1988 Under the influence of homogeneous transcortin samples, a decrease in the content of 5 beta-reduced corticosterone metabolites is revealed to occur depending on transcortin concentration in the system. Corticosterone 100-114 serpin family A member 6 Rattus norvegicus 161-172 3394170-5 1988 The transcortin activity on corticosterone metabolism is supposed to be closely related to the intensity of its complexing with transcortin. Corticosterone 28-42 serpin family A member 6 Rattus norvegicus 4-15 3394170-5 1988 The transcortin activity on corticosterone metabolism is supposed to be closely related to the intensity of its complexing with transcortin. Corticosterone 28-42 serpin family A member 6 Rattus norvegicus 128-139 3386271-4 1988 However, the sequestering influence of transcortin on receptor binding of corticosterone could be demonstrated by the FPLC technique with mixtures containing serum and hippocampus cytosol. Corticosterone 74-88 serpin family A member 6 Rattus norvegicus 39-50 2830101-3 1987 Since molar concentrations of corticosterone produced in the medium were below the transcortin concentration at all levels of stimulation, protein-unbound corticosterone in the medium may have been largely reduced by the addition of transcortin. Corticosterone 30-44 serpin family A member 6 Rattus norvegicus 233-244 2830101-3 1987 Since molar concentrations of corticosterone produced in the medium were below the transcortin concentration at all levels of stimulation, protein-unbound corticosterone in the medium may have been largely reduced by the addition of transcortin. Corticosterone 155-169 serpin family A member 6 Rattus norvegicus 233-244 3040377-0 1987 Plasma adrenocorticotropin is more sensitive than transcortin production or thymus weight to inhibition by corticosterone in rats. Corticosterone 107-121 serpin family A member 6 Rattus norvegicus 50-61 3948773-9 1986 The marked increase in tissue transcortin ([3H]corticosterone binding in the presence of excess dexamethasone) suggested that plasma transcortin is sequestered by peripheral tissues in substantial amounts in the acutely adrenalectomized rat. Corticosterone 47-61 serpin family A member 6 Rattus norvegicus 30-41 3030124-5 1987 Studies in 10-day-old rats, with very low levels of corticosteroid binding globulin (CBG), showed a high degree of aldosterone selectivity in both zones of the kidney, whereas [3H]aldosterone and [3H]corticosterone were equivalently bound in hippocampus. Corticosterone 200-214 serpin family A member 6 Rattus norvegicus 85-88 3029259-8 1987 The results are discussed in the light of a possible specific corticosteroid-binding globulin (CBG) like binding protein of adrenal origin released in conjunction with corticosterone. Corticosterone 168-182 serpin family A member 6 Rattus norvegicus 62-93 3029259-8 1987 The results are discussed in the light of a possible specific corticosteroid-binding globulin (CBG) like binding protein of adrenal origin released in conjunction with corticosterone. Corticosterone 168-182 serpin family A member 6 Rattus norvegicus 95-98 3029259-9 1987 This binding protein has a lower affinity for corticosterone and a shorter half-life than CBG. Corticosterone 46-60 serpin family A member 6 Rattus norvegicus 90-93 3019054-3 1986 The corticosterone binding capacity of the plasma as well as the binding capacity of CBG for corticosterone decreased in intact foetuses for the last 3 days of gestation and stayed very low in pups from day 0 to day 8 postpartum. Corticosterone 93-107 serpin family A member 6 Rattus norvegicus 85-88 3019054-6 1986 The fall in CBG activity in normal rat pups and the subsequent rise in free steroids could explain a sharp decrease in plasma ACTH levels as well as the drop in adrenal and plasma corticosterone concentration. Corticosterone 180-194 serpin family A member 6 Rattus norvegicus 12-15 3551808-7 1987 In vivo studies, in contrast, show that corticosterone is very poorly taken up and/or retained in kidney, colon, parotid, and pituitary (but not in hippocampus) in mature and 10-day-old (minimal transcortin) rats, whereas aldosterone is well taken up and/or retained by all tissues, evidence for tissue-specific aldosterone selectivity in vivo. Corticosterone 40-54 serpin family A member 6 Rattus norvegicus 195-206 3948773-9 1986 The marked increase in tissue transcortin ([3H]corticosterone binding in the presence of excess dexamethasone) suggested that plasma transcortin is sequestered by peripheral tissues in substantial amounts in the acutely adrenalectomized rat. Corticosterone 47-61 serpin family A member 6 Rattus norvegicus 133-144 3003661-6 1986 As hyperthyroidism was associated with marked elevations in the concentration of corticosteroid-binding globulin and in the extent of binding of corticosterone, these results suggest that the effects of both age and thyroid status on serum concentrations of corticosterone may reflect changes in the metabolic clearance of the hormone. Corticosterone 258-272 serpin family A member 6 Rattus norvegicus 81-112 6684831-1 1983 Amount of corticosterone-binding sites in transcortin from blood plasma of intact rats constituted 2960 fmole/mg of protein, in the animals with stress reaction caused by immobilization within 24 hrs--1630 fmole/mg. Corticosterone 10-24 serpin family A member 6 Rattus norvegicus 42-53 6482428-4 1984 Corticosterone also shows highest affinity to plasma transcortin and thymus cytosol in the presence of RU 26988. Corticosterone 0-14 serpin family A member 6 Rattus norvegicus 53-64 6368985-4 1984 It is postulated that the CBG-like molecules participate in the cellular uptake process of corticosterone, thereby modulating the feedback signal of this steroid on pituitary function. Corticosterone 91-105 serpin family A member 6 Rattus norvegicus 26-29 6227474-4 1983 However, due to the very high affinity of CBG for corticosterone at 4 C, this slight contamination resulted in significant alterations in the apparent affinity of steroids competing for aldosterone-binding sites. Corticosterone 50-64 serpin family A member 6 Rattus norvegicus 42-45 6628329-7 1983 The occupancy of this site in vivo may depend on the relative tissue concentrations of aldosterone or corticosterone, which, in turn, are modulated by the levels of extravascular transcortin. Corticosterone 102-116 serpin family A member 6 Rattus norvegicus 179-190 6320679-1 1984 To determine the intrarenal distribution of extravascular corticosteroid-binding globulin- (CBG) like sites, we measured the specific binding of [3H]corticosterone to supernatants prepared from papilla-inner medulla, outer medulla, and cortex from adrenalectomized rats. Corticosterone 149-163 serpin family A member 6 Rattus norvegicus 92-95 6320679-7 1984 In addition, given the higher levels of extravascular than intravascular CBG and the recurrent vascular architecture of the renal medulla-papilla, a countercurrent exchange model is proposed for renewable sequestration of corticosterone in the region. Corticosterone 222-236 serpin family A member 6 Rattus norvegicus 73-76 6853674-5 1983 Corticosterone was used as the model corticosteroid, since this compound binds to CBG with the same affinity as does cortisol, and the brain extraction of corticosterone is more readily measured in vivo than is the brain extraction of cortisol. Corticosterone 0-14 serpin family A member 6 Rattus norvegicus 82-85 6684831-2 1983 Dissociation constants of the complex corticosterone-transcortin were 4.6 nM and 9.3 nM, respectively. Corticosterone 38-52 serpin family A member 6 Rattus norvegicus 53-64 7150966-6 1982 A large portion (approximately 75%) of the transcortin-like [3H]corticosterone binding protein was located in the interstitial space between the sheath and the ganglionic cells. Corticosterone 64-78 serpin family A member 6 Rattus norvegicus 43-54 6298090-4 1983 Competition studies indicate that pituitary transcortin modulates interaction of corticosterone with receptor binding sites and, hence, may interfere with steroid translocation to the nucleus. Corticosterone 81-95 serpin family A member 6 Rattus norvegicus 44-55 7155298-3 1982 This reduction was observed whether corticosterone or dexamethasone was employed as competitor to determine nonspecific binding, thus eliminating transcortin as the cause of the corticosterone effect on binding. Corticosterone 178-192 serpin family A member 6 Rattus norvegicus 146-157 760829-3 1979 Rat serum or insufficiently perfused tissue contained a corticosterone-binding component with pI of 5.2--5.5 representing corticosteroid-binding globulin. Corticosterone 56-70 serpin family A member 6 Rattus norvegicus 122-153 7305760-4 1981 The concentration of corticosteroids and CBG capacity in the plasma was 250-550 micrograms/l and 250-480 micrograms corticosterone bound per litre, respectively, in rats killed during the last 4 days of gestation. Corticosterone 116-130 serpin family A member 6 Rattus norvegicus 41-44 731146-2 1978 The binding characteristics were similar to those exhibited by transcortin: radioactive corticosterone was bound to a greater extent than radioactive dexamethasone and labelled corticosterone, but not labelled dexamethasone, was displaced by unlabelled corticosterone, deoxycorticosterone and progesterone. Corticosterone 88-102 serpin family A member 6 Rattus norvegicus 63-74 731146-2 1978 The binding characteristics were similar to those exhibited by transcortin: radioactive corticosterone was bound to a greater extent than radioactive dexamethasone and labelled corticosterone, but not labelled dexamethasone, was displaced by unlabelled corticosterone, deoxycorticosterone and progesterone. Corticosterone 177-191 serpin family A member 6 Rattus norvegicus 63-74 731146-2 1978 The binding characteristics were similar to those exhibited by transcortin: radioactive corticosterone was bound to a greater extent than radioactive dexamethasone and labelled corticosterone, but not labelled dexamethasone, was displaced by unlabelled corticosterone, deoxycorticosterone and progesterone. Corticosterone 177-191 serpin family A member 6 Rattus norvegicus 63-74 591850-4 1977 These results suggest that corticosterone may be responsible for the observed changes in transcortin concentration. Corticosterone 27-41 serpin family A member 6 Rattus norvegicus 89-100 14006-2 1977 The macromolecules binding corticosterone and its metabolites were characterized as (a) a steroid conjugate-binding (Stokes radius 2.5 nm and sedimentation coefficient 4.1 S in high ionic strength; pI 8.7, (b) transcortin and (c) a glucocorticoid "receptor". Corticosterone 27-41 serpin family A member 6 Rattus norvegicus 210-221 27418032-11 2016 Dynamic changes in the levels and function of CBG likely modulate the tissue availability of corticosterone during inflammation. Corticosterone 93-107 serpin family A member 6 Rattus norvegicus 46-49 182222-1 1976 Using a gel filtration on Sephadex G-150 in low ionic strength, it was possible to separate a corticosterone-binding protein in rat liver cytosol from corticosteroid-binding globulin after incubation of cytosol with [3H]corticosterone. Corticosterone 94-108 serpin family A member 6 Rattus norvegicus 151-182 182222-1 1976 Using a gel filtration on Sephadex G-150 in low ionic strength, it was possible to separate a corticosterone-binding protein in rat liver cytosol from corticosteroid-binding globulin after incubation of cytosol with [3H]corticosterone. Corticosterone 220-234 serpin family A member 6 Rattus norvegicus 151-182 182121-5 1976 Radioactivity eluted in the 0.02 and 0.06M-phosphate regions on DEAE-cellulose DE-52 appears to be due to [3H]aldosterone binding to glucocorticoid-specific "GR" receptors and to transcortin respectively, since labelling was greater with corticosterone even at 10 nM than with the mineralocorticoid at 100nM and since [14C]corticosterone bound to blood serum transcortin was always co-chromatographed in the 0.06M-phosphate region. Corticosterone 238-252 serpin family A member 6 Rattus norvegicus 179-190 182121-5 1976 Radioactivity eluted in the 0.02 and 0.06M-phosphate regions on DEAE-cellulose DE-52 appears to be due to [3H]aldosterone binding to glucocorticoid-specific "GR" receptors and to transcortin respectively, since labelling was greater with corticosterone even at 10 nM than with the mineralocorticoid at 100nM and since [14C]corticosterone bound to blood serum transcortin was always co-chromatographed in the 0.06M-phosphate region. Corticosterone 323-337 serpin family A member 6 Rattus norvegicus 179-190 1188062-0 1975 [Binding of corticosterone to transcortin of the serum of rats at distant period following irradiation]. Corticosterone 12-26 serpin family A member 6 Rattus norvegicus 30-41 167924-4 1975 An increase of the metabolic clearance rate of corticosterone, observed as a function of the infusion rate, was ascribed to saturation by the steroid of the plasma transcortin binding sites. Corticosterone 47-61 serpin family A member 6 Rattus norvegicus 164-175 4354389-0 1973 The role of transcortin in the distribution of corticosterone in the rat. Corticosterone 47-61 serpin family A member 6 Rattus norvegicus 12-23 5665206-0 1968 [Transcortin-corticosterone relationship and control of pituitary-adrenal activity in the rat. Corticosterone 13-27 serpin family A member 6 Rattus norvegicus 1-12 27263429-5 2016 While corticosterone levels were not different among groups, CBG levels were lower in PAE offspring from P1 to P8, suggesting a lower corticosterone reservoir that may underlie susceptibility to inflammation. Corticosterone 134-148 serpin family A member 6 Rattus norvegicus 61-64 174733-4 1976 (2) Gel permeation chrmatography with BioRad A-5M reveals the presence of a [3H] corticosterone-macromolecular complex with an elution volume comparable to transcortin as well as a very large hormone-binding complex eluting in the void volume of the column... Corticosterone 81-95 serpin family A member 6 Rattus norvegicus 156-167 1233956-4 1975 A close correlation was found to exist between the concentration of total corticosterone in the blood plasma and CBG. Corticosterone 74-88 serpin family A member 6 Rattus norvegicus 113-116 1233956-5 1975 Increases in the total concentration of corticosterone in blood plasma are, in 84% of all cases, brought about by increases in CBG concentrations. Corticosterone 40-54 serpin family A member 6 Rattus norvegicus 127-130 32932938-5 2020 A single stress exposure produced a significant increase in the expression of corticosterone reactivator, 11-beta-hydroxysteroid dehydrogenase 1 (11beta-Hsd1), while the 11beta-Hsd2 isozyme and corticosteroid-binding globulin were down-regulated following stress, indicative of an elevated availability of active corticosterone. Corticosterone 78-92 serpin family A member 6 Rattus norvegicus 194-225