SOME ASPECTS OF ZONATION AND FUNCTION OF THE ADRENAL CORTEX

1954 ◽  
Vol 10 (3) ◽  
pp. 245-NP ◽  
Author(s):  
I. CHESTER JONES ◽  
C. C. ROBY

SUMMARY Male adult mice, 80 days after hypophysectomy, show approximately the same pattern of sodium and potassium intake and sodium, potassium and water output as normal mice. The healthy remnant of adrenal cortex left after the operation is thought to be responsible for the day-to-day competence of the hypophysectomized animal in salt-electrolyte metabolism. The histology of the cortex is described and it is shown that, with the injection of ACTH, a cortex of normal appearance can be regenerated from the persistent zona glomerulosa of the long-term hypophysectomized mouse.

1954 ◽  
Vol 10 (3) ◽  
pp. 262-265 ◽  
Author(s):  
I. CHESTER JONES ◽  
A. WRIGHT

SUMMARY Male adult rats, with established drinking patterns, were given the choice of saline or tap water to drink, immediately after adrenal enucleation. Both saline and water were taken, but by the 6th day after operation the rats had returned to drinking predominantly tap water. The adrenals at this stage showed a small compact cortex, no distinguishable zona glomerulosa, and they appeared to be composed for the most part of cells in 'fascicles'. Adrenalectomized animals chose saline, drinking more and more pari passu with time. Other short-term enucleated animals were injected with ACTH, and the tendency for the regenerating cortex to form in 'fascicles' was very pronounced.


1954 ◽  
Vol 10 (3) ◽  
pp. 251-261 ◽  
Author(s):  
I. CHESTER JONES ◽  
MARGARET H. SPALDING

SUMMARY Male adult rats whose adrenals were enucleated and allowed to regenerate showed in one group normal competence to handle administered water loads, and in another a slow diuresis after this functional test. In the latter case the predisposing factor is cortical insufficiency and not the absence of the medulla. Even those animals with regenerated enucleated adrenals, which gave a normal response to water loads, nevertheless still showed some differences from normal in regard to sodium and potassium metabolism. The histology of the adrenals in the different groups is described.


Circulation ◽  
2012 ◽  
Vol 125 (suppl_10) ◽  
Author(s):  
Zefeng Zhang ◽  
Mary Cogswell ◽  
Cathleen Gillespie ◽  
Jing Fang ◽  
Shifan Dai ◽  
...  

Introduction: Evidence from randomized controlled trials demonstrates higher sodium and/or lower potassium intake increase blood pressure and the risk of hypertension. However, the relationship between sodium, potassium and blood pressure has not been examined using nationally representative sample and estimated usual intakes of these nutrients. Hypothesis: We hypothesized that usual sodium and potassium intake have opposing effects on blood pressure and a higher sodium-to-potassium ratio is associated with elevated blood pressure and hypertension. Methods: We analyzed data on 12,854 participants aged 20 years and older from the 2003-2008 National Health and Nutrition Examination Surveys. We estimated the usual intakes of sodium and potassium from the diet accounting for measurement error. Mean blood pressure was calculated from up to three readings on each subject and hypertension included both diagnosed and undiagnosed hypertension. We used multivariable linear regression to examine the associations between intakes of sodium, potassium and their ratio with systolic and diastolic blood pressure, and logistic regression for associations with hypertension. Results: The average estimated usual intakes of sodium and potassium were 3465 and 2741 mg/d, respectively. The average sodium-to-potassium ratio was 1.39; higher ratios were observed among males, younger and non-Hispanic black participants. After adjustment for potential confounders, usual intakes of sodium, potassium and their ratio were significantly associated with systolic blood pressure, with an increase of 1.08 mm Hg (95% confidence interval (CI): 0.30 – 1.86) and a decrease of 1.47 mmHg (95% CI: -2.31, -0.63) for every 1000 mg/d increase in sodium and potassium intake, respectively, and an increase of 2.80 mmHg (95% CI: 0.90 - 4.70) for every unit increase in sodium-to-potassium ratio. No association was found for diastolic blood pressure. The adjusted odds ratio (OR) comparing the highest and lowest quartiles of usual sodium or potassium intakes were 1.63 (95% CI: 1.14 - 2.34) and 0.61 (95% CI: 0.45 - 0.82), respectively, for risk of hypertension. For sodium-to-potassium ratio, the adjusted OR was 1.49 (95% CI: 1.17 - 1.89). The patterns of association were largely consistent across age, gender, race/ethnicity, body mass index, and education subgroups. Conclusions: In conclusion, our results indicated higher sodium and lower potassium intakes were associated with increased systolic blood pressure and risk for hypertension. The combined effect of sodium and potassium might play a central role in the pathogenesis of hypertension. The results further confirm that reducing sodium and increasing potassium intakes concurrently may have important implications in the prevention of hypertension, and hence, of cardiovascular disease.


2022 ◽  
pp. 109980042110654
Author(s):  
María Correa-Rodríguez ◽  
Sara DelOlmo-Romero ◽  
Gabriela Pocovi-Gerardino ◽  
José-Luis Callejas-Rubio ◽  
Raquel Ríos-Fernández ◽  
...  

Purpose: The aim of this study was to investigate the association between dietary sodium, potassium, and sodium:potassium ratio and clinical disease activity parameters, damage accrual, and cardiovascular disease risk factors in a population of patients with systemic lupus erythematous (SLE). Research design and study sample: A cross-sectional study including a total of 280 patients was conducted (90.4% females; mean age 46.9 ± 12.85 years). Data collection: The SLE Disease Activity Index (SLEDAI-2K) and the SDI Damage Index were used to assess disease activity and disease-related damage, respectively. A 24-hour diet recall was used to estimate dietary intake of sodium and potassium. Results: Dietary sodium intake was significantly associated with anti-dsDNA ( β  =  −.005; 95% CI [.002 .008]; p = .001) and complement C4 level ( β  =  −.002; 95% CI [−.003, .000]; p = .039). Dietary potassium intake was also significantly associated with complement C3 level ( β  =  −.004; 95% CI [−.007, −.001]; p = .021). Multiple logistic regression models revealed a positive association between dietary sodium intake and the risk of having hsCRP > 3 ( p = .005) and an inverse association between dietary potassium intake and the risk of having hsCRP > 3 ( p = .004). Conclusions: SLE patients with higher dietary sodium and lower dietary potassium intakes had an increased risk of higher hsCRP. Dietary sodium intake was significantly associated with anti-dsDNA and complement C4 level, while dietary potassium intake was associated with complement C3 level, supporting that dietary sodium and potassium intakes might play a key role in markers related to disease activity in SLE patients.


1983 ◽  
Vol 245 (5) ◽  
pp. E449-E456
Author(s):  
C. Meuli ◽  
J. Muller

Late steps of aldosterone biosynthesis, i.e., the conversions of corticosterone to 18-hydroxycorticosterone and aldosterone, are catalyzed by a mitochondrial cytochrome P-450. Resumption of potassium intake by potassium-depleted rats resulted within 2 days in a marked stimulation of these conversions, as reflected by increased production of aldosterone and 18-hydroxycorticosterone and decreased outputs of deoxycorticosterone, corticosterone, and 18-hydroxy-11-deoxycorticosterone by incubated capsular portions of the adrenal glands. The stimulation of aldosterone biosynthesis was accompanied by the appearance of a protein with a molecular weight of about 49,000 in the mitochondria of the zona glomerulosa but not of the inner zones of the adrenal cortex. Over 48 h of potassium repletion, the amount of this protein increased in parallel with the activity of the final steps of aldosterone biosynthesis. According to its molecular weight, its zone specificity, and the time course of its appearance, this protein might represent the steroid 18-methyl oxidase (cytochrome P-450CMO for corticosterone methyl oxidase) that catalyzes the conversion of corticosterone to 18-hydroxycorticosterone and aldosterone.


Circulation ◽  
2013 ◽  
Vol 127 (suppl_12) ◽  
Author(s):  
Angelo Campanozzi ◽  
Sonia Avallone ◽  
Daniela Galeone ◽  
Pasquale Strazzullo

Introduction: The MINISAL survey aimed to assess the age-, gender- and region-specific habitul sodium and potassium intake and its association with relevant anthropometric characteristics in a national sample of Italian healthy children and adolescents referred to centers recognised by the Italian Society of Gastroenterology and Pediatric Nutrition. Methods: The study population included 1422 6 to 18 yrs. old subjects from ten regions. Main anthropometric indexes, blood pressure (BP) and 24h urinary sodium and potassium excretion (as proxy for habitual sodium and potassium intake) were measured using carefully standardised procedures. Potentially incomplete 24h collections were identified and excluded from the analysis based on values of urinary creatinine/Kg body weight and/or a urinary volume below the 5 th percentile of the overall distribution. The analysis was carried out upon stratification by gender (M=788, F=644), puberal age category: <9 yrs, 9-11 yrs. and 5 months, >11 yrs. and 5 mo. (male); < 8 yrs., 8-10 yrs. and 2 mo., > 10 yrs. and 2 mo. (female), and scholar age category: 6-10 yrs., 11-13 yrs. and 14-18 yrs (both male and female participants). The relationships among body weight, sodium, potassium and creatinine excretion were analysed using Z-scores as an index of body mass. Results: The 24h sodium and potassium excretion were higher in male than in female participants (respectively, 130±63 vs 119±56 mmol; p=0.001 and 39±18 vs 37±16 mmol; p=0.003). Upon stratification by puberal age and gender, 24h urinary sodium and potassium excretion were respectively 109±54 and 36±19 mol in category 1, 134±60 and 40±16 in category 2 and 152±69 and 43±17 in category 3 for male subjects (p<0.01); 98±39 and 33±13 in category 1, 105±45 and 34±13 in category 2 and 137±63 and 40±18 mmol in category 3 for female individuals (p<0.05). The expected gender difference in 24h urinary creatinine was observed in all age categories (p<0.05). Male individuals had consistently greater sodium, potassium and creatinine excretion than female individuals (p between <0.001 and <0.05). Upon stratification of the study population in four body weight categories (BMI Z-score <0, 0 to <0,9, 1 to <1,9 and ≥2), 24h sodium excretion was significantly greater in obese compared to normal weight children. 24h potassium excretion was also greater in obese children and adolescents compared with their normal weight counterparts (p=0.002). No significant difference was observed in either sodium or potassium excretion by geographical area. Conclusions: The MINISAL survey indicates a substantial age-, gender- and body mass-related variation with average values of sodium intake definitely high when related to true physiological needs or to the “adequate intakes” defined by the health institutions. By contrast, the habitual potassium intake was relatively low and such to indicate an inadequate fruit and vegetable consumption.


Endocrinology ◽  
2017 ◽  
Vol 159 (2) ◽  
pp. 579-596 ◽  
Author(s):  
Isabella Finco ◽  
Antonio M Lerario ◽  
Gary D Hammer

Abstract The atrophy and hypofunction of the adrenal cortex following long-term pharmacologic glucocorticoid therapy is a major health problem necessitating chronic glucocorticoid replacement that often prolongs the ultimate return of endogenous adrenocortical function. Underlying this functional recovery is anatomic regeneration, the cellular and molecular mechanisms of which are poorly understood. Investigating the lineage contribution of cortical Sonic hedgehog (Shh)+ progenitor cells and the SHH–responsive capsular Gli1+ cells to the regenerating adrenal cortex, we observed a spatially and temporally bimodal contribution of both cell types to adrenocortical regeneration following cessation of glucocorticoid treatment. First, an early repopulation of the cortex is defined by a marked delamination and expansion of capsular Gli1+ cells, recapitulating the establishment of the capsular-cortical homeostatic niche during embryonic development. This rapid repopulation is promptly cleared from the cortical compartment only to be supplanted by repopulating cortical cells derived from the resident long-term-retained zona glomerulosa Shh+ progenitors. Pharmacologic and genetic dissection of SHH signaling further defines an SHH-dependent activation of WNT signaling that supports regeneration of the cortex following long-term glucocorticoid therapy. We define the signaling and lineage relationships that underlie the regeneration process.


2020 ◽  
Author(s):  
Matija Sestan-Pesa ◽  
Marya Shanabrough ◽  
Tamas L. Horvath ◽  
Maria Consolata Miletta

AbstractAs marijuana use during adolescence has been increasing, the need to understand the effects of its long-term use becomes crucial. Previous research suggested that marijuana consumption during adolescence increases the risk of developing mental illness, such as schizophrenia, depression, and anxiety. Ghrelin is a peptide produced primarily in the gut and is important for feeding behavior. Recent studies have shown that ghrelin and its receptor, the growth hormone secretagogue receptor (GHSR) play important roles in mediating stress, as well as anxiety and, depression-like behaviors in animal models. Here, we investigated the effects of chronic Tetrahydrocannabinol (THC) administration during adolescence (P42-55), in GHSR (GHSR-/-) knockout mice and their wild type littermates in relation to anxiety-like behaviors. We found that continuous THC exposure during peri-adolescence did not lead to any significant alterations in anxiety-like behavior of male adult mice, regardless of genotype. These data indicate that in the presence of intact GHSR signaling, THC exposure during peri-adolescence has limited if any long term impact on anxiety-like behaviors in mice.


1973 ◽  
Vol 73 (1) ◽  
pp. 80-90 ◽  
Author(s):  
Jürg Müller ◽  
Klaus Baumann

ABSTRACT Capsular adrenals ("zona glomerulosa") of rats which had been kept on a sodium- and potassium-deficient diet and which were markedly hypokalaemic, converted tritiated corticosterone to 18-hydroxycorticosterone and aldosterone, and tritiated cortexolone to cortisol at the same respective rates as the capsular adrenals of sodium- and potassium-replete animals. Aldosterone production from endogenous precursors was elevated under basal conditions of incubation, but not under stimulation by added serotonin. Corticosterone and deoxycorticosterone outputs were normal during incubation with or without serotonin. Capsular adrenals of rats which had been kept first on a potassium-deficient diet for two weeks and then on a sodium- and potassium-deficient diet for two weeks converted 18 times more tritiated corticosterone to 18-hydroxycorticosterone and aldosterone and produced 5 times more aldosterone from endogenous precursors than the tissue of rats which had been kept on the potassium-deficient diet for the whole period, although the serum potassium was similarly low in both groups. These results indicate that under simple potassium restriction as well as under combined sodium and potassium restriction, neither the plasma potassium concentration nor the total body potassium is the only regulator of the activity of the enzymes involved in the final steps of aldosterone biosynthesis.


1986 ◽  
Vol 112 (3) ◽  
pp. 404-408 ◽  
Author(s):  
Claudia Robba ◽  
Piera Rebuffat ◽  
Giuseppina Mazzocchi ◽  
Gastone G. Nussdorfer

Abstract. The effects of α-melanocyte-stimulating hormone (α-MSH) on the rat adrenal cortex were investigated by coupled morphometric and radioimmunological techniques. Short-term α-MSH administration provoked a significant increase in the aldosterone plasma level along with a notable lipid droplet depletion in zona glomerulosa cells. Long-term α-MSH treatment induced a notable hypertrophy of zona glomerulosa cells and a further rise in the blood concentration of aldosterone. α-MSH did not affect zona fasciculata morphology and corticosterone plasma level. The possibility is discussed that α-MSH may be specifically involved in the control of the growth and steroidogenic capacity of rat adrenal zona glomerulosa.


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