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1.
Chinese Acupuncture & Moxibustion ; (12): 525-532, 2022.
Article in Chinese | WPRIM | ID: wpr-927418

ABSTRACT

OBJECTIVE@#To observe the effect of wheat-grain moxibustion on behavior, 5-hydroxytryptamine (5-HT) and cortisol in the serum, mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) in the hippocampus in rats with hypothyroidism complicated with depression, and to explore the possible mechanism of wheat-grain moxibustion on improving depression in rats with hypothyroidism.@*METHODS@#A total of 32 SPF SD rats were randomly divided into a blank group, a model group, a medication group and a wheat-grain moxibustion group, 8 rats in each group. Except for the blank group, the rats in the remaining groups were treated with intragastric administration of 0.1% propylthiouracil (PTU) suspension at 1 mL/100 g, once a day for 4 weeks to establish the rat model of hypothyroidism, and whether the rats were accompanied with depression-like behavior determined through behavioristics evaluation. The rats in the medication group were intervened with euthyrox at 0.9 mL/100 g, once a day, for 4 weeks; the rats in the wheat-grain moxibustion group were treated with wheat-grain moxibustion at "Dazhui" (GV 14), "Mingmen" (GV 4), "Shenshu" (BL 23) and "Pishu" (BL 20), 7 cones each acupoint, once a day, six times a week for 4 weeks. After the intervention, the depression status was observed by behavioristics test; the contents of thyroid stimulating hormone (TSH), total thyroxine (TT4), 5-HT and cortisol in the serum were detected by ELISA; the protein expressions of MR and GR in hippocampus were detected by Western blot; the expressions of MR mRNA and GR mRNA in the hippocampus were detected by real-time PCR.@*RESULTS@#Before the intervention, compared with the blank group, the scores of open field test (OFT) were decreased and the immobility time of tail suspension test (TST) was prolonged (P<0.05); the serum TSH contents were increased and TT4 contents were decreased (P<0.01) in the other three groups. After the intervention, compared with the model group, the vertical score of OFT was increased and the immobility time of forced swimming test (FST) was prolonged in the medication group (P<0.05), while the scores of three items of OFT were increased (P<0.05, P<0.01), and the immobility time of FST and TST was shortened in the wheat-grain moxibustion group (P<0.01, P<0.05). Compared with the medication group, the immobility time of TST and FST in the wheat-grain moxibustion group was shorter (P<0.05, P<0.01). Compared with the blank group, in the model group, the contents of serum TSH and cortisol were increased (P<0.01, P<0.001), while the contents of serum TT4 and 5-HT were decreased (P<0.01, P<0.001). Compared with the model group, the contents of serum TT4 and 5-HT were increased, while the contents of serum TSH and cortisol were decreased in the medication group and wheat-grain moxibustion group (P<0.01, P<0.05). Compared with the blank group, the protein and mRNA expression of MR, GR in the hippocampus in the model group was decreased (P<0.01, P<0.05, P<0.001); compared with the model group, the protein and mRNA expression of MR in the hippocampus in the medication group were increased (P<0.05), and the protein expression of MR, GR and mRNA expression of MR in the hippocampus in the wheat-grain moxibustion group were increased (P<0.05, P<0.01). Compared with the medication group, the expression of MR mRNA in the wheat-grain moxibustion group was increased (P<0.05).@*CONCLUSION@#Wheat-grain moxibustion could significantly improve thyroid function and depression in rats with hypothyroidism. Its mechanism may be related to up-regulating the protein and mRNA expression of MR and GR in the hippocampus, and then affecting the expression of serum cortisol and 5-HT.


Subject(s)
Animals , Rats , Acupuncture Points , Depression/therapy , Hippocampus/metabolism , Hydrocortisone/metabolism , Hypothyroidism/therapy , Moxibustion , RNA, Messenger/metabolism , Rats, Sprague-Dawley , Receptors, Glucocorticoid/metabolism , Receptors, Mineralocorticoid/metabolism , Serotonin , Thyrotropin/metabolism , Triticum/metabolism
2.
Rev. méd. Chile ; 147(4): 490-498, abr. 2019. tab, graf
Article in Spanish | LILACS | ID: biblio-1014251

ABSTRACT

The renin-angiotensin-aldosterone system modulates volume, sodium and potassium homeostasis. In the setting of a high sodium diet, up to 30% of patients with hypertension have a low or suppressed renin and increased volume. This phenotype of low renin hypertension (LRH) is multifactorial and includes infrequent inherited genetic syndromes, milder phenotypes of classic diseases and environmental exposures. All these conditions have in common a higher cardiovascular risk mediated by the over activation of the mineralocorticoid receptor (MR), present not only in the kidney, but also in vasculature, myocardium and adipocytes. Consequently, the aim of LRH treatment goes beyond the control of blood pressure and requires antagonizing MR with specific pharmacologic agents, pursuing normalization of renin as a clinical objective. Due to the unusual evaluation of renin status by non-endocrinologists and lack of disease awareness, only a minority of hypertensive patients receive this pathophysiologically-driven treatment that should reduce cardiovascular outcomes.


Subject(s)
Humans , Renin-Angiotensin System/physiology , Hypertension/metabolism , Hypertension/therapy , Renin/metabolism , Receptors, Mineralocorticoid/metabolism , Disease Management , Aldosterone/metabolism , Hypertension/physiopathology
3.
Rev. bras. enferm ; 68(2): 219-227, Mar-Apr/2015. tab
Article in Spanish | LILACS, BDENF | ID: lil-752507

ABSTRACT

RESUMEN Objetivo: estudio cualitativo que siguió los principios de la teoría fundamentada con el fin de analizar la identidad profesional de docentes de enfermería por medio del análisis de incidentes críticos que más las desestabilizaban. Método: entrevistas semi-estructuradas fueron realizadas a siete enfermeras que actúan como docentes e investigadoras en una universidad privada de Barcelona. Resultados: el material empírico resultante fue organizado en dos categorías: caracterización de los incidentes críticos y reacción de las enfermeras frente a ellos. Conclusión: se concluye que la identidad profesional de estas enfermeras en el campo académico está aún en construcción y que la inexperiencia es el mayor obstáculo que enfrentan para gestionar los incidentes críticos en el trabajo docente. .


RESUMO Objetivo: estudo qualitativo que seguiu os princípios da teoria fundamentada em dados com o objetivo de analisar a identidade profissional de docentes de enfermagem por meio da análise de incidentes críticos que mais as desestabilizaram. Método: entrevistas semiestruturadas foram realizadas com sete enfermeiras que atuam como docentes e pesquisadoras em uma universidade privada de Barcelona. Resultados: o material empírico resultante foi organizado em duas categorias: caracterização dos incidentes críticos e reação das enfermeiras frente a eles. Conclusão: concluiu-se que identidade profissional dessas enfermeiras no campo acadêmico está ainda em construção e a que inexperiência é o maior obstáculo que enfrentam para gerenciar incidentes críticos no trabalho docente. .


ABSTRACT Objective: a qualitative study that followed the principles of the grounded theory in order to analyze the professional identity of nursing academics through the analysis of the most disturbing critical incidents. Method: semi-structured interviews were conducted with seven nurses who worked as professors and researchers in a private university in Barcelona. Results: the resulting empirical material was organized into two categories: characterization of critical incidents and responsiveness to the incident. Conclusion: the professional identity of nurses regarding the academic area is still under construction and inexperience is the major obstacle in the management of critical incidents in the teaching career. .


Subject(s)
Humans , DNA , Receptors, Glucocorticoid/chemistry , Receptors, Mineralocorticoid/chemistry , Amino Acid Sequence , Crystallography, X-Ray , DNA , Escherichia coli/genetics , Escherichia coli/metabolism , Gene Expression , Molecular Sequence Data , Mutation , Neoplasms/genetics , Neoplasms/metabolism , Neoplasms/pathology , Protein Structure, Secondary , Protein Structure, Tertiary , Pseudohypoaldosteronism/genetics , Pseudohypoaldosteronism/metabolism , Pseudohypoaldosteronism/pathology , Receptors, Glucocorticoid/genetics , Receptors, Glucocorticoid/metabolism , Receptors, Mineralocorticoid/genetics , Receptors, Mineralocorticoid/metabolism , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Sequence Alignment , Structural Homology, Protein
4.
Arq. bras. endocrinol. metab ; 51(3): 373-381, abr. 2007. ilus
Article in Portuguese | LILACS | ID: lil-452177

ABSTRACT

Pseudo-hipoaldosteronismo tipo 1 (PHA1) é uma doença genética rara, caracterizada por vômitos, desidratação, baixo ganho pôndero-estatural e perda urinária de sal no período neonatal. Indivíduos afetados apresentam hiponatremia, hipercalemia, aumento da atividade de renina plasmática e concentrações muito elevadas de aldosterona plasmática, secundárias a uma resistência renal ou sistêmica à aldosterona. A forma sistêmica do PHA1 é a mais grave, havendo necessidade de reposição de doses altas de NaCl. Os sintomas persistem por toda a vida. Mutações inativadoras nos genes codificadores das sub-unidades do canal de sódio sensível à amilorida (ENaC) em homozigose ou heterozigose composta são responsáveis pelo quadro clínico de PHA1 sistêmico. A forma renal do PHA1 tem apresentação clínica mais leve, com necessidade de suplementação de doses baixas de NaCl. Os sintomas regridem no final do primeiro ano de vida. Mutações inativadoras do gene do receptor do mineralocorticóide (MR) estão associadas à forma renal do PHA1 em várias famílias afetadas. O padrão de herança é autossômico dominante, entretanto casos esporádicos têm sido relatados. No presente trabalho, discutimos as ações e os mecanismos de ação da aldosterona, e os aspectos clínicos e fisiopatológicos envolvidos nas síndromes de resistência aos mineralocorticóides. Adicionalmente, os aspectos clínicos e moleculares de uma família brasileira com PHA1 secundário à mutação R947X no gene do MR são discutidos.


Pseudohypoaldosteronism type 1 (PHA1) is a rare genetic disease characterized by neonatal renal salt wasting, vomiting, dehydration and failure to thrive. Affected patients present hyponatremia, hyperkalemia, associated with high levels of plasma renin and aldosterone resulting from a renal or systemic resistance to aldosterone. The systemic form of PHA1 results in a severe phenotype, and high doses of salt supplementation are necessary. The symptoms are life-long recurrent. This form is associated with autosomal recessive transmission. Homozygous or compound heterozygous loss of function mutations in the genes coding for the epithelial sodium channel (ENaC) subunities are responsible for this disease. The renal form of PHA1 results in a mild phenotype. Low doses of salt supplementation are required and usually the symptoms remit at the end of the first year of life. Heterozygous loss-of-function mutations in the mineralocorticoid receptor (MR) gene are associated with the renal form of PHA1 in the majority of the affected families but sporadic cases have been reported. In this review the mechanisms of aldosterone action and its effects are discussed. Additionally, clinical and molecular findings of a Brazilian family with the renal form of PHA1 caused by a nonsense mutation (R947X) in the MR gene are presented.


Subject(s)
Humans , Infant, Newborn , Male , Aldosterone/blood , Pseudohypoaldosteronism/genetics , Receptors, Mineralocorticoid/genetics , Aldosterone/physiology , Epithelial Sodium Channels/genetics , Mutation , Pedigree , Pseudohypoaldosteronism/metabolism , Pseudohypoaldosteronism/physiopathology , Receptors, Mineralocorticoid/metabolism , Transcription, Genetic
5.
Journal of Korean Medical Science ; : 805-811, 2004.
Article in English | WPRIM | ID: wpr-27632

ABSTRACT

The effect of aldosterone on connective tissue growth factor (CTGF) was examined in rat embryonic ventricular myocytes. Upon aldosterone treatment, CTGF expression was significantly increased in a dose and time-dependent manner. To explore the molecular mechanism for this upregulation, we examined the role of mineralocorticoid receptor. Pre-treatment of an antagonist (spironolactone) at 5-fold excess of aldosterone blocked the CTGF induction by aldosterone, suggesting that the upregulation was mediated by mineralocorticoid receptor. Aldosterone treatment resulted in activation of ERK1/2, p38 MAPK, and JNK pathways with a more transient pat-tern in p38 MAPK. Blocking studies using pre-treatment of the inhibitor of each path-way revealed that p38 MAPK cascade may be important for aldosterone-mediated CTGF upregulation as evidenced by the blocking of CTGF induction by SB203580 (p38 MAPK inhibitor), but not by PD098059 (ERK1/2 inhibitor) and JNK inhibitor I. Interestingly, JNK inhibitor I and PD098059 decreased the basal level of CTGF expression. On the other hand, pre-treatment of spironolactone abrogated the p38 MAPK activation, indicating that mineralocorticoid receptor mechanism is linked to p38 MAPK pathway. Taken together, our findings suggest that aldosterone induces CTGF expression via both p38 MAPK cascade and mineralocorticoid receptor and that cross-talk exists between the two pathways.


Subject(s)
Animals , Rats , Aldosterone/pharmacology , Cells, Cultured , Dose-Response Relationship, Drug , Gene Expression Regulation/drug effects , Heart Ventricles/drug effects , Immediate-Early Proteins/metabolism , Intercellular Signaling Peptides and Proteins/metabolism , Myocytes, Cardiac/drug effects , Receptors, Mineralocorticoid/metabolism , Signal Transduction/drug effects , Spironolactone/pharmacology , Up-Regulation/drug effects , p38 Mitogen-Activated Protein Kinases/metabolism
6.
Braz. j. med. biol. res ; 25(12): 1153-62, 1992. ilus, tab
Article in English | LILACS | ID: lil-134494

ABSTRACT

Adrenocortical hormone effects in the central nervous system depend on steroid interaction with intracellular receptors, which belong to a superfamily of ligand-activated transcription factors. Using a combination of biochemical and molecular biology techniques, we have demonstrated: 1. the localization of mineralocorticoid receptors in the brain, with highest density present in hippocampus, lateral septum and some amygdaloid nuclei; 2. the arousal of a mineralocorticoid-specific behavior such as salt appetite, coincident with inhibition of the biosynthesis/activity of (Na+K)ATPase in some amygdaloid and hypothalamic nuclei; 3. the modulation of the biosynthesis/activity of the sodium pump by glucocorticoids, although for these hormones changes are stimulatory, as shown in the spinal cord and brain; 4. the reported steroid effects on the (Na+K)ATPase constitute an important mechanism of control of nervous system function, involving behavior, changes in excitability and neurotropism


Subject(s)
Animals , Appetite Regulation/physiology , Brain/physiology , Mineralocorticoids/metabolism , Sodium Chloride, Dietary/metabolism , Appetite Regulation/drug effects , Brain/drug effects , Glucocorticoids/pharmacology , Sodium-Potassium-Exchanging ATPase/drug effects , Sodium-Potassium-Exchanging ATPase/metabolism , Rats , Receptors, Mineralocorticoid/drug effects , Receptors, Mineralocorticoid/metabolism
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