13 results on '"Kanogwun Thongchote"'
Search Results
2. Effects of scapulothoracic exercises on chest mobility, respiratory muscle strength, and pulmonary function in male COPD patients with forward shoulder posture: a randomized control trial
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Kanogwun Thongchote, Usa Chinwaro, and Sarawut Lapmanee
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General Immunology and Microbiology ,General Medicine ,General Pharmacology, Toxicology and Pharmaceutics ,General Biochemistry, Genetics and Molecular Biology - Abstract
Background The postural abnormality, forward shoulder posture (FSP), is the most common cause of respiratory impairment in older individuals with chronic obstructive pulmonary disease (COPD). A recent study found that performing pectoral stretching and scapular strengthening exercises for eight weeks could reduce FSP in healthy participants. We aimed to determine the effects of pectoral stretching and scapular stabilizer strengthening exercises on FSP, chest wall mobility, respiratory muscle strength, and pulmonary function in male patients with COPD. Methods This study was randomized clinical trial. Forty male COPD patients with FSP aged 60–90 years were included and randomly allocated to control (n=20) and exercise (n=20) groups. Following completion of the scapulothoracic exercises (three days/week, for eight weeks), respiratory functions were assessed by measuring the magnitude of FSP, chest mobility, respiratory muscle strength, and pulmonary functions. Results FSP and thoracic kyphosis angle significantly decreased compared to controls (p Conclusions The eight-week combined pectoral muscles self-stretching and serratus anterior and lower trapezius strengthening exercises could be an effective treatment and/or prevention strategy for FSP reduction, leading to improved respiratory function in male COPD patients.
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- 2022
3. 1,25-Dihydroxyvitamin D3-induced intestinal calcium transport is impaired inβ-globin knockout thalassemic mice
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Jarinthorn Teerapornpuntakit, Nateetip Krishnamra, Saovaros Svasti, Kanogwun Thongchote, Pissared Khuituan, Kamonshanok Kraidith, and Narattaphol Charoenphandhu
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Calcium metabolism ,medicine.medical_specialty ,Ussing chamber ,Chemistry ,Clinical Biochemistry ,chemistry.chemical_element ,Transporter ,Cell Biology ,General Medicine ,Calcium ,Biochemistry ,Subcutaneous injection ,Endocrinology ,medicine.anatomical_structure ,Internal medicine ,Vitamin D and neurology ,medicine ,Duodenum ,Globin - Abstract
Besides being a common haematological disorder caused by a reduction in β-globin production, β-thalassemia has been reported to impair body calcium homeostasis, leading to massive bone loss and increased fracture risk. Here, we demonstrated that heterozygous β-globin knockout thalassemic mice had a lower rate of duodenal calcium absorption compared with the wild-type littermates, whereas the epithelial electrical parameters, including transepithelial resistance, were not affected, suggesting no change in the epithelial integrity and permeability. Daily subcutaneous injection of 1 µg kg−1 1,25-dihydroxyvitamin D3 [1,25(OH)2D3] for 3 days enhanced the duodenal calcium absorption in wild-type, but not in thalassemic mice. Although β-thalassemia increased the mRNA level of divalent metal transporter-1, an iron transporter in the duodenum, it had no effect on the transcripts of ferroportin-1 or the principal calcium transporters. In conclusion, β-thalassemia impaired the 1,25(OH)2D3-dependent intestinal calcium absorption at the post-transcriptional level, which, in turn, contributed to the dysregulation of body calcium metabolism and β-thalassemia-induced osteopenia. Copyright © 2013 John Wiley & Sons, Ltd.
- Published
- 2013
4. Transcriptome responses of duodenal epithelial cells to prolactin in pituitary-grafted rats
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Kanogwun Thongchote, Kannikar Wongdee, Jarinthorn Teerapornpuntakit, Nateetip Krishnamra, and Narattaphol Charoenphandhu
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medicine.medical_specialty ,Cell signaling ,Duodenum ,Receptors, Prolactin ,Biology ,Biochemistry ,Rats, Sprague-Dawley ,Transcriptome ,Endocrinology ,Anterior pituitary ,Pituitary Gland, Anterior ,Internal medicine ,medicine ,Cellular metabolic process ,Animals ,Cluster Analysis ,Transplantation, Homologous ,Intestinal Mucosa ,Molecular Biology ,Oligonucleotide Array Sequence Analysis ,Microarray analysis techniques ,Gene Expression Profiling ,Epithelial Cells ,Prolactin ,Rats ,Cell biology ,Transplantation ,Gene expression profiling ,medicine.anatomical_structure ,Gene Expression Regulation ,Female - Abstract
Chronic prolactin (PRL) exposure can affect several functions of duodenal epithelia, especially those associated with fluid and electrolyte transport. However, little is known regarding its molecular mechanism. To identify PRL-regulated genes, microarray analysis was performed on RNA samples from duodenal epithelial cells of anterior pituitary (AP)-grafted hyperprolactinemic rats. Herein, we identified 321 transcripts upregulated and 241 transcripts downregulated after 4 weeks of AP transplantation. Results from real-time PCR analyses of 15 selected genes were consistent with the microarray results. Gene ontology analysis demonstrated pleiotropic effects of PRL on several cellular processes, including cellular metabolic process, cell communication and cell adhesion. Interestingly, 17 upregulated transcripts and 12 downregulated transcripts are involved in the transport of ions and nutrients, e.g., Ca(2+), Na(+), K(+), Cl(-) and glucose, thus agreeing with the established action of PRL on electrolyte homeostasis. The present results provided fundamental information for further investigations on mechanism of PRL actions in the intestine.
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- 2008
5. Prolactin decreases expression of Runx2, osteoprotegerin, and RANKL in primary osteoblasts derived from tibiae of adult female rats
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Methajit MethawasinM. Methawasin, Kannikar Wongdee, Nateetip Krishnamra, Kanogwun Thongchote, Jarinthorn Teerapornpuntakit, and Narattaphol Charoenphandhu
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musculoskeletal diseases ,endocrine system ,medicine.medical_specialty ,Transcription, Genetic ,Physiology ,Osteocalcin ,Cell Culture Techniques ,Down-Regulation ,Core Binding Factor Alpha 1 Subunit ,Polymerase Chain Reaction ,Rats, Sprague-Dawley ,Calcification, Physiologic ,Osteoprotegerin ,Physiology (medical) ,Lactation ,Internal medicine ,medicine ,Animals ,RNA, Messenger ,Osteopontin ,Cells, Cultured ,Prolactinoma ,Pharmacology ,Osteoblasts ,Dose-Response Relationship, Drug ,Tibia ,biology ,RANK Ligand ,Osteoblast ,General Medicine ,medicine.disease ,Prolactin ,Rats ,Endocrinology ,medicine.anatomical_structure ,RANKL ,biology.protein ,Female ,hormones, hormone substitutes, and hormone antagonists - Abstract
Hyperprolactinemia caused by physiological or pathological conditions, such as those occurring during lactation and prolactinoma, respectively, results in progressive osteopenia. The underlying mechanisms, however, are controversial. Prolactin (PRL) may directly attenuate the functions of osteoblasts, since these bone cells express PRL receptors. The present study therefore aimed to investigate the effects of PRL on the expression of genes related to the osteoblast functions by using quantitative real-time PCR technique. Herein, we used primary osteoblasts that were derived from the tibiae of adult rats and displayed characteristics of differentiated osteoblasts, including in vitro mineralization. Osteoblasts exposed for 48 h to 1000 ng/mL PRL, but not to 10 or 100 ng/mL PRL, showed decreases in the mRNA expression of Runx2, osteoprotegerin (OPG), and receptor activator of nuclear factor κB ligand (RANKL) by 60.49%, 72.74%, and 87.51%, respectively. Nevertheless, PRL did not change the RANKL/OPG ratio, since expression of OPG and RANKL were proportionally decreased. These concentrations of PRL had no effect on the mRNA expression of osteocalcin and osteopontin, nor on mineralization. High pathologic concentrations of PRL (1000 ng/mL) may downregulate expression of genes that are essential for osteoblast differentiation and functions. The present results explained the clinical findings of hyperprolactinemia-induced bone loss.
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- 2008
6. Prolactin directly enhances bone turnover by raising osteoblast-expressed receptor activator of nuclear factor κB ligand/osteoprotegerin ratio
- Author
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Jarinthorn Teerapornpuntakit, Kanogwun Thongchote, Dutmanee Seriwatanachai, Jantarima Pandaranandaka, Tuangporn Suthiphongchai, Narattaphol Charoenphandhu, Nateetip Krishnamra, and Kukiat Tudpor
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musculoskeletal diseases ,endocrine system ,medicine.medical_specialty ,Histology ,Bone density ,Receptors, Prolactin ,Physiology ,Ovariectomy ,Endocrinology, Diabetes and Metabolism ,Osteoclasts ,Dexamethasone ,Bone resorption ,Cell Line ,Bone remodeling ,Rats, Sprague-Dawley ,Absorptiometry, Photon ,Osteoprotegerin ,Bone Density ,Pituitary Gland, Anterior ,Osteoclast ,Internal medicine ,medicine ,Animals ,Humans ,Vitamin D ,Glucocorticoids ,Bone mineral ,Osteoblasts ,biology ,Chemistry ,RANK Ligand ,Uterus ,Estrogens ,Osteoblast ,Organ Size ,Prolactin ,Rats ,Hyperprolactinemia ,medicine.anatomical_structure ,Endocrinology ,RANKL ,biology.protein ,Female ,Bone Remodeling ,Biomarkers ,hormones, hormone substitutes, and hormone antagonists - Abstract
Hyperprolactinemia leads to high bone turnover as a result of enhanced bone formation and resorption. Although its osteopenic effect has long been explained as hyperprolactinemia-induced hypogonadism, identified prolactin (PRL) receptors in osteoblasts suggested a possible direct action of PRL on bone. In the present study, we found that hyperprolactinemia induced by anterior pituitary transplantation (AP), with or without ovariectomy (Ovx), had no detectable effect on bone mineral density and content measured by dual-energy X-ray absorptiometry (DXA). However, histomorphometric studies revealed increases in the osteoblast and osteoclast surfaces in the AP rats, but a decrease in the osteoblast surface in the AP+Ovx rats. The resorptive activity was predominant since bone volume and trabecular number were decreased, and the trabecular separation was increased in both groups. Estrogen supplement (E2) fully reversed the effect of estrogen depletion in the Ovx but not in the AP+Ovx rats. In contrast to the typical Ovx rats, bone formation and resorption became uncoupled in the AP+Ovx rats. Therefore, hyperprolactinemia was likely to have some estrogen-independent and/or direct actions on bone turnover. Osteoblast-expressed PRL receptor transcripts and proteins shown in the present study confirmed our hypothesis. Furthermore, we demonstrated that the osteoblast-like cells, MG-63, directly exposed to PRL exhibited lower expression of alkaline phosphatase and osteocalcin mRNA, and a decrease in alkaline phosphatase activity. The ratios of receptor activator of nuclear factor kappaB ligand (RANKL) and osteoprotegerin (OPG) proteins were increased, indicating an increase in the osteoclastic bone resorption. The present data thus demonstrated that hyperprolactinemia could act directly on bone to stimulate bone turnover, with more influence on bone resorption than formation. PRL enhanced bone resorption in part by increasing RANKL and decreasing OPG expressions by osteoblasts.
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- 2008
7. High Physiological Prolactin Induced by Pituitary Transplantation Decreases BMD and BMC in the Femoral Metaphysis, but Not in the Diaphysis of Adult Female Rats
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Nateetip Krishnamra, Kanogwun Thongchote, and Narattaphol Charoenphandhu
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musculoskeletal diseases ,endocrine system ,medicine.medical_specialty ,Physiology ,Ovariectomy ,Long bone ,Metaphysis ,Bone remodeling ,Rats, Sprague-Dawley ,Bone Density ,Internal medicine ,medicine ,Animals ,Femur ,Bone mineral ,Lumbar Vertebrae ,Estradiol ,business.industry ,Body Weight ,Anatomy ,musculoskeletal system ,medicine.disease ,Prolactin ,Rats ,Osteopenia ,Transplantation ,Bone Diseases, Metabolic ,Diaphysis ,Endocrinology ,medicine.anatomical_structure ,Pituitary Gland ,Calcium ,Female ,Diaphyses ,business ,hormones, hormone substitutes, and hormone antagonists - Abstract
High physiological prolactin (PRL) stimulated intestinal calcium absorption and renal calcium uptake in mammals. Previous histomorphometric study revealed a significant increase in bone turnover in the trabecular part of the PRL-exposed long (cortical) bone; however, whole-bone densitometric analysis was unable to demonstrate such effect. We therefore studied differential changes in bone mineral density (BMD) and contents (BMC) of the femoral diaphysis and metaphysis in adult female rats exposed to high PRL induced by anterior pituitary (AP) transplantation. The estrogen-dependent effects of PRL on the femur were also investigated. We found that chronic exposure to PRL had no effect on BMD or BMC of the femoral diaphysis, which represented the cortical part of the long bone. It is interesting that 7 weeks after an AP transplantation, BMD and BMC of the femoral metaphysis were significantly decreased by 8% and 14%, respectively. Ovariectomy (Ovx) for 2, 5, and 7 weeks also decreased BMD and BMC in the femoral metaphysis, but not in the diaphysis. However, the AP transplantation plus Ovx (AP+Ovx) produced no additive effects. Nevertheless, 2.5 microg/kg 17beta-estradiol (E2) supplementation abolished the osteopenic effects of both Ovx and AP+Ovx on the femur. As for the L5-6 vertebrae, BMD and BMC were not affected by PRL exposure, but were significantly decreased by Ovx and AP+Ovx, and such decreases were completely prevented by E2 supplementation. It could be concluded that high physiological PRL induced a significant osteopenia in the trabecular part, i.e., the metaphysis, of the femora of adult female rats in an estrogen-dependent manner. Since PRL had no detectable effect on the vertebrae, the effects of PRL on bone appeared to be site-specific.
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- 2008
8. Bone microstructural defects and osteopenia in hemizygous βIVSII-654 knockin thalassemic mice: sex-dependent changes in bone density and osteoclast function
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Narattaphol Charoenphandhu, Kanogwun Thongchote, Nateetip Krishnamra, Jarinthorn Teerapornpuntakit, Saovaros Svasti, and Panan Suntornsaratoon
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Male ,medicine.medical_specialty ,Aging ,Bone density ,Chemical Phenomena ,Physiology ,Endocrinology, Diabetes and Metabolism ,Injections, Subcutaneous ,Osteoporosis ,Osteoclasts ,Mice, Transgenic ,Bone and Bones ,Osteoclast ,Bone Density ,Physiology (medical) ,Internal medicine ,medicine ,Animals ,Gene Knock-In Techniques ,Growth Plate ,Crosses, Genetic ,Fluorescent Dyes ,Mechanical Phenomena ,Bone mineral ,Sex Characteristics ,business.industry ,beta-Thalassemia ,Beta thalassemia ,medicine.disease ,Fluoresceins ,Osteopenia ,Mice, Inbred C57BL ,medicine.anatomical_structure ,Endocrinology ,Female ,Analysis of variance ,business ,Sex characteristics - Abstract
β-Thalassemia, a hereditary anemic disorder, is often associated with skeletal complications that can be found in both males and females. The present study aimed to investigate the age- and sex-dependent changes in bone mineral density (BMD) and trabecular microstructure in βIVSII-654knockin thalassemic mice. Dual-energy X-ray absorptiometry and computer-assisted bone histomorphometry were employed to investigate temporal changes in BMD and histomorphometric parameters in male and female mice of a βIVSII-654knockin mouse model of human β-thalassemia, in which impaired splicing of β-globin transcript was caused by hemizygous C→T mutation at nucleotide 654 of intron 2. Young, growing βIVSII-654mice (1 mo old) manifested shorter bone length and lower BMD than their wild-type littermates, indicating possible growth retardation and osteopenia, the latter of which persisted until 8 mo of age (adult mice). Interestingly, two-way analysis of variance suggested an interaction between sex and βIVSII-654genotype, i.e., more severe osteopenia in adult female mice. Bone histomorphometry further suggested that low trabecular bone volume in male βIVSII-654mice, particularly during a growing period (1–2 mo), was primarily due to suppression of bone formation, whereas both a low bone formation rate and a marked increase in osteoclast surface were observed in female βIVSII-654mice. In conclusion, osteopenia and trabecular microstructural defects were present in both male and female βIVSII-654knockin thalassemic mice, but the severity, disease progression, and cellular mechanism differed between the sexes.
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- 2015
9. Running exercise alleviates trabecular bone loss and osteopenia in hemizygous β-globin knockout thalassemic mice
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Kanogwun Thongchote, Jarinthorn Teerapornpuntakit, Narattaphol Charoenphandhu, Nateetip Krishnamra, and Saovaros Svasti
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Male ,medicine.medical_specialty ,Aging ,Physiology ,Endocrinology, Diabetes and Metabolism ,Osteoporosis ,Interleukin-1beta ,Physical Exertion ,beta-Globins ,Motor Activity ,Bone erosion ,Bone and Bones ,Mice ,Random Allocation ,Absorptiometry, Photon ,Endurance training ,Bone Density ,Physiology (medical) ,Internal medicine ,Interleukin-1alpha ,medicine ,Animals ,Globin ,Bone Resorption ,Hemizygote ,Mice, Knockout ,Sex Characteristics ,business.industry ,medicine.disease ,Up-Regulation ,Osteopenia ,Mice, Inbred C57BL ,Trabecular bone ,Bone Diseases, Metabolic ,Endocrinology ,medicine.anatomical_structure ,Bone histomorphometry ,Thalassemia ,Female ,Bone marrow ,business - Abstract
A marked decrease in β-globin production led to β-thalassemia, a hereditary anemic disease associated with bone marrow expansion, bone erosion, and osteoporosis. Herein, we aimed to investigate changes in bone mineral density (BMD) and trabecular microstructure in hemizygous β-globin knockout thalassemic (BKO) mice and to determine whether endurance running (60 min/day, 5 days/wk for 12 wk in running wheels) could effectively alleviate bone loss in BKO mice. Both male and female BKO mice (1–2 mo old) showed growth retardation as indicated by smaller body weight and femoral length than their wild-type littermates. A decrease in BMD was more severe in female than in male BKO mice. Bone histomorphometry revealed that BKO mice had decreases in trabecular bone volume, trabecular number, and trabecular thickness, presumably due to suppression of osteoblast-mediated bone formation and activation of osteoclast-mediated bone resorption, the latter of which was consistent with elevated serum levels of osteoclastogenic cytokines IL-1α and -1β. As determined by peripheral quantitative computed tomography, running increased cortical density and thickness in the femoral and tibial diaphyses of BKO mice compared with those of sedentary BKO mice. Several histomorphometric parameters suggested an enhancement of bone formation (e.g., increased mineral apposition rate) and suppression of bone resorption (e.g., decreased osteoclast surface), which led to increases in trabecular bone volume and trabecular thickness in running BKO mice. In conclusion, BKO mice exhibited pervasive osteopenia and impaired bone microstructure, whereas running exercise appeared to be an effective intervention in alleviating bone microstructural defect in β-thalassemia.
- Published
- 2014
10. 1,25-Dihydroxyvitamin D3 -induced intestinal calcium transport is impaired in β-globin knockout thalassemic mice
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Narattaphol, Charoenphandhu, Kamonshanok, Kraidith, Jarinthorn, Teerapornpuntakit, Kanogwun, Thongchote, Pissared, Khuituan, Saovaros, Svasti, and Nateetip, Krishnamra
- Subjects
Male ,Mice, Knockout ,Ion Transport ,Injections, Subcutaneous ,beta-Thalassemia ,beta-Globins ,Intestines ,Mice, Inbred C57BL ,Mice ,Structure-Activity Relationship ,Calcitriol ,Animals ,Calcium ,Female ,Intestinal Mucosa - Abstract
Besides being a common haematological disorder caused by a reduction in β-globin production, β-thalassemia has been reported to impair body calcium homeostasis, leading to massive bone loss and increased fracture risk. Here, we demonstrated that heterozygous β-globin knockout thalassemic mice had a lower rate of duodenal calcium absorption compared with the wild-type littermates, whereas the epithelial electrical parameters, including transepithelial resistance, were not affected, suggesting no change in the epithelial integrity and permeability. Daily subcutaneous injection of 1 µg kg(-1) 1,25-dihydroxyvitamin D3 [1,25(OH)2 D3 ] for 3 days enhanced the duodenal calcium absorption in wild-type, but not in thalassemic mice. Although β-thalassemia increased the mRNA level of divalent metal transporter-1, an iron transporter in the duodenum, it had no effect on the transcripts of ferroportin-1 or the principal calcium transporters. In conclusion, β-thalassemia impaired the 1,25(OH)2 D3 -dependent intestinal calcium absorption at the post-transcriptional level, which, in turn, contributed to the dysregulation of body calcium metabolism and β-thalassemia-induced osteopenia.
- Published
- 2012
11. Impaired bone formation and osteopenia in heterozygous β(IVSII-654) knockin thalassemic mice
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Kanogwun Thongchote, Mayurachat Sa-ardrit, Suthat Fucharoen, Nateetip Krishnamra, Narattaphol Charoenphandhu, and Saovaros Svasti
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musculoskeletal diseases ,Male ,medicine.medical_specialty ,Heterozygote ,Histology ,Medullary cavity ,beta-Globins ,Bone resorption ,Mice ,Absorptiometry, Photon ,Osteoclast ,Osteogenesis ,Internal medicine ,medicine ,Animals ,Gene Knock-In Techniques ,Molecular Biology ,Bone mineral ,Osteoid ,Chemistry ,beta-Thalassemia ,Osteoblast ,Cell Biology ,Anatomy ,medicine.disease ,Osteopenia ,Mice, Inbred C57BL ,Medical Laboratory Technology ,Bone Diseases, Metabolic ,Disease Models, Animal ,medicine.anatomical_structure ,Endocrinology ,Mutation ,Cortical bone - Abstract
β-thalassemia caused by the C→T mutation at nucleotide 654 of the intron 2 (β(IVSII-654)) results in aberrant splicing of β-globin RNA, leading to an almost absence of β-globin synthesis. Although trabecular and cortical bone loss was previously reported in β-thalassemic mice with deletion of β-globin gene, the microscopic changes in trabecular structure in β(IVSII-654) thalassemic mice remained elusive. Here, we investigated the macroscopic and microscopic bone changes in 12-week-old β(IVSII-654) knockin thalassemic mice by dual-energy X-ray absorptiometry (DXA) and histomorphometric analysis, respectively. DXA revealed a decrease in bone mineral density in the lumbar vertebrae and tibial metaphysis, but not in the femoral diaphysis, suggesting that β(IVSII-654) thalassemia predominantly led to osteopenia at the trabecular site, but not the cortical site. Further histomorphometric analysis of the tibial secondary spongiosa showed that trabecular bone volume was significantly decreased with the expansion of marrow cavity. Decreases in osteoblast surface, osteoid surface, mineral apposition rate, mineralizing surface, and mineralized volume were also observed. Moreover, trabecular bone resorption was markedly enhanced as indicated by increases in the osteoclast surface and eroded surface. It could be concluded that β(IVSII-654) thalassemia impaired bone formation and enhanced bone resorption, thereby leading to osteopenia especially at the trabecular sites, such as the tibial metaphysis.
- Published
- 2011
12. Two-step stimulation of intestinal Ca(2+) absorption during lactation by long-term prolactin exposure and suckling-induced prolactin surge
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Kamonshanok Kraidith, Kanogwun Thongchote, Narongrit Thongon, Jarinthorn Teerapornpuntakit, La-iad Nakkrasae, Narattaphol Charoenphandhu, and Nateetip Krishnamra
- Subjects
medicine.medical_specialty ,Pituitary gland ,Time Factors ,Physiology ,Duodenum ,Endocrinology, Diabetes and Metabolism ,Stimulation ,Biology ,Rats, Sprague-Dawley ,Pregnancy ,Physiology (medical) ,Lactation ,Internal medicine ,medicine ,Animals ,Humans ,Intestinal Mucosa ,Fetus ,Prolactin ,Electric Stimulation ,Animals, Suckling ,Rats ,Transplantation ,Endocrinology ,medicine.anatomical_structure ,Intestinal Absorption ,Sucking Behavior ,Calcium ,Female ,Caco-2 Cells ,Endocrine gland ,Hormone - Abstract
During pregnancy and lactation, the enhanced intestinal Ca2+absorption serves to provide Ca2+for fetal development and lactogenesis; however, the responsible hormone and its mechanisms remain elusive. We elucidated herein that prolactin (PRL) markedly stimulated the transcellular and paracellular Ca2+transport in the duodenum of pregnant and lactating rats as well as in Caco-2 monolayer in a two-step manner. Specifically, a long-term exposure to PRL in pregnancy and lactation induced an adaptation in duodenal cells at genomic levels by upregulating the expression of genes related to transcellular transport, e.g., TRPV5/6 and calbindin-D9k, and the paracellular transport, e.g., claudin-3, thereby raising Ca2+absorption rate to a new “baseline” (Step 1). During suckling, PRL surge further increased Ca2+absorption to a higher level (Step 2) in a nongenomic manner to match Ca2+loss in milk. PRL-enhanced apical Ca2+uptake was responsible for the increased transcellular transport, whereas PRL-enhanced paracellular transport required claudin-15, which regulated epithelial cation selectivity and paracellular Ca2+movement. Such nongenomic PRL actions were mediated by phosphoinositide 3-kinase, protein kinase C, and RhoA-associated coiled-coil-forming kinase pathways. In conclusion, two-step stimulation of intestinal Ca2+absorption resulted from long-term PRL exposure, which upregulated Ca2+transporter genes to elevate the transport baseline, and the suckling-induced transient PRL surge, which further increased Ca2+transport to the maximal capacity. The present findings also suggested that Ca2+supplementation at 15–30 min prior to breastfeeding may best benefit the lactating mother, since more Ca2+could be absorbed as a result of the suckling-induced PRL surge.
- Published
- 2009
13. High-calcium diet modulates effects of long-term prolactin exposure on the cortical bone calcium content in ovariectomized rats
- Author
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Kanogwun Thongchote, Supaporn Puntheeranurak, Wasana Saengamnart, Kukiat Tudpor, Narattaphol Charoenphandhu, and Nateetip Krishnamra
- Subjects
medicine.medical_specialty ,Physiology ,Receptors, Prolactin ,Endocrinology, Diabetes and Metabolism ,Ovariectomy ,chemistry.chemical_element ,Calcium ,Time ,Excretion ,Rats, Sprague-Dawley ,Bone Density ,Physiology (medical) ,Internal medicine ,medicine ,Animals ,Transplantation, Homologous ,Femur ,Calcium metabolism ,Tibia ,Prolactin receptor ,Prolactin ,Rats ,Transplantation ,Calcium, Dietary ,Endocrinology ,medicine.anatomical_structure ,chemistry ,Pituitary Gland ,Ovariectomized rat ,Cortical bone ,Female ,Bone Remodeling - Abstract
High physiological prolactin induced positive calcium balance by stimulating intestinal calcium absorption, reducing renal calcium excretion, and increasing bone calcium deposition in female rats. Although prolactin-induced increase in trabecular bone calcium deposition was absent after ovariectomy, its effects on cortical bones were still controversial. The present investigation, therefore, aimed to study the effect of in vivo long-term high physiological prolactin induced by either anterior pituitary (AP) transplantation or 2.5 mg/kg prolactin injection on cortical bones in ovariectomized rats. Since the presence of prolactin receptors (PRLR) in different bones of normal adult rats has not been reported, we first determined mRNA expression of both short- and long-form PRLRs at the cortical sites (tibia and femur) and trabecular sites (calvaria and vertebrae) by using the RT-PCR. Our results showed the mRNA expression of both PRLR isoforms with predominant long form at all sites. However, high prolactin levels induced by AP transplantation in normal rats did not have any effect on the femoral bone mineral density or bone mineral content. By using45Ca kinetic study, 2.5 mg/kg prolactin did not alter bone formation, bone resorption, calcium deposition, and total calcium content in tibia and femur of adult ovariectomized rats. AP transplantation also had no effect on the cortical total calcium content in adult ovariectomized rats. Because previous work showed that the effects of prolactin were age dependent and could be modulated by high-calcium diet, interactions between prolactin and these two parameters were investigated. The results demonstrated that 2.0% wt/wt high-calcium diet significantly increased the tibial total calcium content in 9-wk-old young AP-grafted ovariectomized rats but decreased the tibial total calcium content in 22-wk-old adult rats. As for the vertebrae, the total calcium contents in both young and adult rats were not changed by high-calcium diet. The present results thus indicated that the adult cortical bones were potentially direct targets of prolactin. Moreover, the effects of high physiological prolactin on cortical bones were age dependent and were observed only under the modulation of high-calcium diet condition.
- Published
- 2006
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