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Role of growth hormone in experimental phosphorus deprivation in the rat
Insights
Eliminating growth and growth hormone (GH) in rats did not prevent most physiological effects of phosphorus deprivation (PD). However, hypophysectomy did prevent hypercalcemia in rats fed a low-phosphorus diet.
Area of Science:
- Endocrinology
- Nutritional Physiology
- Mineral Metabolism
Background:
- Growth demands can worsen phosphorus deprivation (PD).
- Growth hormone (GH) plays a role in physiological responses to nutrient deficiencies.
- Understanding the interplay between growth, GH, and PD is crucial for metabolic health.
Purpose of the Study:
- To investigate if eliminating growth and GH prevents PD-associated changes in young rats.
- To determine if PD in normal rats is linked to increased GH secretion.
- To differentiate the roles of growth and GH in phosphorus and calcium metabolism during PD.
Main Methods:
- Hypophysectomy (HPX) was performed on rats to eliminate growth and GH.
- Rats (intact and HPX) were fed diets with normal phosphorus (NP), low phosphorus (LP), or NP pair-fed (NP-PF).
- Physiological parameters including serum/urinary phosphorus and calcium, intestinal calcium retention, and duodenal uptake of phosphorus and calcium were measured.
Main Results:
- HPX did not prevent most PD-induced physiological changes, such as decreased serum/urinary phosphorus and increased urinary calcium.
- Intestinal calcium retention decreased, and duodenal calcium uptake increased in response to PD, regardless of HPX.
- HPX prevented hypercalcemia observed in intact rats fed an LP diet.
- GH secretion showed no consistent or specific alteration in response to PD in intact rats.
Conclusions:
- Physiological responses to phosphorus deprivation are largely independent of growth and growth hormone, except for hypercalcemia.
- Growth hormone secretion is not consistently altered by phosphorus deprivation in intact rats.
- The elimination of growth and GH does not prevent the majority of physiological adaptations to phosphorus deficiency.
Abstract:
The demands of growth are known to exacerbate the effect of phosphorus deprivation (PD). We examined whether changes associated with PD could be prevented in young rats in which growth and growth hormone (GH) were eliminated by hypophysectomy (HPX) and whether PD in normal intact rats (INT) was associated with increased secretion of GH. INT or thyroxine- and ACTH-replaced HPX rats were fed one of the three diets: 0.31% P (NP); 0.027% P (LP), and 0.31% P, pair-fed with LP-mates (NP-PF). The results indicate that HPX did not qualitatively alter several physiologic responses to PD: (a) serum and urinary phosphorus (P) decreased and urinary calcium (Ca) increased; (b) net intestinal Ca retention fell and duodenal sac uptake of 45Ca rose; and (c) external P balance was restored and duodenal sac uptake of 32P-phosphate increased. Only the hypercalcemia seen in INT, LP rats was prevented by HPX. In INT rats serum immunoassayable GH levels, measured in single samples, were not different between different dietary groups while pituitary bioassayable GH was reduced in both LP and NP-PF rats when compared to the NP rats. Thus, except for hypercalcemia, the physiologic responses associated with PD are not prevented by the elimination of growth and GH, and the development of these responses in INT rats was not associated with a consistent or specific alteration in GH secretion.
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