Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males. / Juel Mortensen, Li; Kooij, Ireen; Lorenzen, Mette; Rye Jørgensen, Niklas; Røder, Andreas; Jørgensen, Anne; Andersson, Anna Maria; Juul, Anders; Blomberg Jensen, Martin.

I: Cell Calcium, Bind 122, 102908, 2024.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Juel Mortensen, L, Kooij, I, Lorenzen, M, Rye Jørgensen, N, Røder, A, Jørgensen, A, Andersson, AM, Juul, A & Blomberg Jensen, M 2024, 'Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males', Cell Calcium, bind 122, 102908. https://doi.org/10.1016/j.ceca.2024.102908

APA

Juel Mortensen, L., Kooij, I., Lorenzen, M., Rye Jørgensen, N., Røder, A., Jørgensen, A., Andersson, A. M., Juul, A., & Blomberg Jensen, M. (2024). Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males. Cell Calcium, 122, [102908]. https://doi.org/10.1016/j.ceca.2024.102908

Vancouver

Juel Mortensen L, Kooij I, Lorenzen M, Rye Jørgensen N, Røder A, Jørgensen A o.a. Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males. Cell Calcium. 2024;122. 102908. https://doi.org/10.1016/j.ceca.2024.102908

Author

Juel Mortensen, Li ; Kooij, Ireen ; Lorenzen, Mette ; Rye Jørgensen, Niklas ; Røder, Andreas ; Jørgensen, Anne ; Andersson, Anna Maria ; Juul, Anders ; Blomberg Jensen, Martin. / Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males. I: Cell Calcium. 2024 ; Bind 122.

Bibtex

@article{025d4146f8a24ff0bf38a8f4dc274f8d,
title = "Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males",
abstract = "Animal and human studies have suggested that sex steroids have calciotropic actions, and it has been proposed that follicle-stimulating hormone (FSH) may exert direct effects on bone. Here, we demonstrate the expression of the receptor for Luteinizing hormone (LH) and human choriogonadotropin (hCG), LHCGR, in human kidney tissue, suggesting a potential influence on calcium homeostasis. To investigate the role of LHCGR agonist on calcium homeostasis in vivo, we conducted studies in male mice and human subjects. Male mice were treated with luteinizing hormone (LH), and human extrapolation was achieved by injecting 5000 IU hCG once to healthy men or men with hypergonadotropic or hypogonadotropic hypogonadism. In mice, LH treatment significantly increased urinary calcium excretion and induced a secondary increase in serum parathyroid hormone (PTH). Similarly, hCG treatment in healthy men led to a significant increase in urinary calcium excretion, serum PTH levels, and 1,25 (OH)2D3, while calcitonin, and albumin levels were reduced, possibly to avoid development of persistent hypocalcemia. Still, the rapid initial decline in ionized calcium coincided with a significant prolongation of the cardiac QTc-interval that normalized over time. The observed effects may be attributed to LH/hCG-receptor (LHCGR) activation, considering the presence of LHCGR expression in human kidney tissue, and the increase in sex steroids occurred several hours after the changes in calcium homeostasis. Our translational study shed light on the intricate relationship between gonadotropins, sex hormones and calcium, suggesting that LHCGR may be influencing calcium homeostasis directly or indirectly.",
keywords = "Calcium, Calcium homeostasis, Endocrine cross-talk, Excretion, Human chorionic gonadotropin, LHCGR expression, Luteinizing hormone, Males, Translational research",
author = "{Juel Mortensen}, Li and Ireen Kooij and Mette Lorenzen and {Rye J{\o}rgensen}, Niklas and Andreas R{\o}der and Anne J{\o}rgensen and Andersson, {Anna Maria} and Anders Juul and {Blomberg Jensen}, Martin",
note = "Publisher Copyright: {\textcopyright} 2024",
year = "2024",
doi = "10.1016/j.ceca.2024.102908",
language = "English",
volume = "122",
journal = "Cell Calcium",
issn = "0143-4160",
publisher = "Churchill Livingstone",

}

RIS

TY - JOUR

T1 - Injection of luteinizing hormone or human chorionic gonadotropin increases calcium excretion and serum PTH in males

AU - Juel Mortensen, Li

AU - Kooij, Ireen

AU - Lorenzen, Mette

AU - Rye Jørgensen, Niklas

AU - Røder, Andreas

AU - Jørgensen, Anne

AU - Andersson, Anna Maria

AU - Juul, Anders

AU - Blomberg Jensen, Martin

N1 - Publisher Copyright: © 2024

PY - 2024

Y1 - 2024

N2 - Animal and human studies have suggested that sex steroids have calciotropic actions, and it has been proposed that follicle-stimulating hormone (FSH) may exert direct effects on bone. Here, we demonstrate the expression of the receptor for Luteinizing hormone (LH) and human choriogonadotropin (hCG), LHCGR, in human kidney tissue, suggesting a potential influence on calcium homeostasis. To investigate the role of LHCGR agonist on calcium homeostasis in vivo, we conducted studies in male mice and human subjects. Male mice were treated with luteinizing hormone (LH), and human extrapolation was achieved by injecting 5000 IU hCG once to healthy men or men with hypergonadotropic or hypogonadotropic hypogonadism. In mice, LH treatment significantly increased urinary calcium excretion and induced a secondary increase in serum parathyroid hormone (PTH). Similarly, hCG treatment in healthy men led to a significant increase in urinary calcium excretion, serum PTH levels, and 1,25 (OH)2D3, while calcitonin, and albumin levels were reduced, possibly to avoid development of persistent hypocalcemia. Still, the rapid initial decline in ionized calcium coincided with a significant prolongation of the cardiac QTc-interval that normalized over time. The observed effects may be attributed to LH/hCG-receptor (LHCGR) activation, considering the presence of LHCGR expression in human kidney tissue, and the increase in sex steroids occurred several hours after the changes in calcium homeostasis. Our translational study shed light on the intricate relationship between gonadotropins, sex hormones and calcium, suggesting that LHCGR may be influencing calcium homeostasis directly or indirectly.

AB - Animal and human studies have suggested that sex steroids have calciotropic actions, and it has been proposed that follicle-stimulating hormone (FSH) may exert direct effects on bone. Here, we demonstrate the expression of the receptor for Luteinizing hormone (LH) and human choriogonadotropin (hCG), LHCGR, in human kidney tissue, suggesting a potential influence on calcium homeostasis. To investigate the role of LHCGR agonist on calcium homeostasis in vivo, we conducted studies in male mice and human subjects. Male mice were treated with luteinizing hormone (LH), and human extrapolation was achieved by injecting 5000 IU hCG once to healthy men or men with hypergonadotropic or hypogonadotropic hypogonadism. In mice, LH treatment significantly increased urinary calcium excretion and induced a secondary increase in serum parathyroid hormone (PTH). Similarly, hCG treatment in healthy men led to a significant increase in urinary calcium excretion, serum PTH levels, and 1,25 (OH)2D3, while calcitonin, and albumin levels were reduced, possibly to avoid development of persistent hypocalcemia. Still, the rapid initial decline in ionized calcium coincided with a significant prolongation of the cardiac QTc-interval that normalized over time. The observed effects may be attributed to LH/hCG-receptor (LHCGR) activation, considering the presence of LHCGR expression in human kidney tissue, and the increase in sex steroids occurred several hours after the changes in calcium homeostasis. Our translational study shed light on the intricate relationship between gonadotropins, sex hormones and calcium, suggesting that LHCGR may be influencing calcium homeostasis directly or indirectly.

KW - Calcium

KW - Calcium homeostasis

KW - Endocrine cross-talk

KW - Excretion

KW - Human chorionic gonadotropin

KW - LHCGR expression

KW - Luteinizing hormone

KW - Males

KW - Translational research

U2 - 10.1016/j.ceca.2024.102908

DO - 10.1016/j.ceca.2024.102908

M3 - Journal article

C2 - 38852333

AN - SCOPUS:85195369032

VL - 122

JO - Cell Calcium

JF - Cell Calcium

SN - 0143-4160

M1 - 102908

ER -

ID: 395072313