Growth hormone (GH), also known as somatotropin or human growth hormone, is a peptide hormone produced by the pituitary glands anterior lobe. It promotes the development of virtually all bodily tissues, including bone. Somatotrophs, anterior pituitary cells that produce and secrete GH, release one to two milligrams of the hormone every day. GH is required for optimal physical growth in children; its levels build gradually during infancy and peak during puberty growth spurt.
GH’s Full Form
GH’s full form is Growth Hormone. The pituitary gland is a brain organ that generates many specialised hormones, including growth hormone (also referred to as human growth hormone). Growth hormone influences our height and aids in developing our bones and muscles. Growth hormone levels change throughout the day, evidently affected by physical activity. When we exercise, for example, our levels rise.
Growth hormone levels rise during childhood and reach their highest point during puberty. The formation hormone encourages bone and cartilage growth throughout this stage of development. Growth hormone governs fat, muscle, tissue, and bone in our bodies and other parts of our metabolism, including insulin action and blood sugar levels throughout our lives. From middle age forward, growth hormone levels usually decline.
Doctors often prescribe synthetic growth hormone to assist youngsters with low hormone levels to attain their maximum height. However, there is a black market for synthetic growth hormone, notably among athletes, bodybuilders, and people whose self-esteem is based on muscular appearance. These persons may believe that taking growth hormone (in conjunction with other muscle-building medications) will increase their muscle strength. Other muscle-building drugs, such as steroids, are responsible for any increase in muscular strength.
How GH Works
Growth hormone is required for our bones to stretch to adult dimensions during development and adolescence. In addition, our liver produces insulin-like growth factors in response to growth hormones. Therefore, bone development is aided by this and other related chemicals.
Growth Hormone for Children
Some youngsters may not produce enough natural growth hormones to reach their full potential. However, they can achieve their full height by taking synthesised growth hormones. Children may take human growth hormone in situations of inadequate development due to growth hormone deficiency, Turner syndrome, or renal failure. However, research shows that unless a kid has very high growth hormone levels and consumes the synthesised form, they will not grow any taller than they would have grown naturally. Therefore, before being administered any medicine for their ailment, children suffering stunted or delayed growth should have their natural growth hormone levels evaluated by medical authorities.
Growth Hormone Deficiency
Various factors, including GH deficiency, can cause short height and dwarfism. It is caused by injury to the hypothalamus or pituitary gland during foetal development (congenital GH deficit) or after delivery (postnatal GH deficiency) (acquired GH deficiency). Mutations in genes that control GH production and secretion can also cause GH deficiency. PIT-1 (pituitary-specific transcription factor-1) and POUF-1 are two genes that are affected (prophet of PIT-1). Other pituitary hormones’ production and secretion may be affected by mutations in these genes. In certain circumstances, GH shortage is caused by a lack of GHRH, in which case GHRH infusion might help boost GH production.
In certain situations, the somatotrophs cannot produce GH, or the hormone is structurally aberrant and has limited growth-promoting action. In addition, children with psychosocial dwarfism, caused by severe emotional deprivation, frequently have low height and GH insufficiency. However, endocrine function and development rate normalise when children with this disease are removed from a stressful, nonnurturing environment.
The size of children with isolated GH deficiency is average at birth, but growth retardation appears within the first two years of life. Compared to the patient’s chronological age, radiographs (X-ray images) of the epiphyses (growing ends) of bones demonstrate growth retardation. Although puberty is frequently delayed in afflicted women, fertility and normal childbirth are achievable.
Growth Hormone Excess
A benign tumour (adenoma) of the pituitary gland’s somatotroph cells most commonly causes excessive GH production. For example, a lung or pancreatic islet of Langerhans tumour can create GHRH, which induces the somatotrophs to release enormous levels of GH. Ectopic GH synthesis (generation by tumour cells in tissues where GH is not usually synthesised) might result from more than the hormone in rare situations. Somatotroph tumours in children are highly uncommon and produce rapid development, resulting in gigantism and acromegaly-like symptoms.
Acromegaly is a condition in which the body’s distal (acral) portions, such as the hands, feet, chin, and nose, grow. Overgrowth of cartilage, muscle, subcutaneous tissue, and skin causes enlargement. As a result, acromegaly sufferers have a prominent jaw, a huge nose, enormous hands and feet, and growth of most other tissues, such as the tongue, heart, liver, and kidneys. In addition, a pituitary tumour can induce severe headaches, and pressure on the optic chiasm can cause vision abnormalities and the symptoms of excess GH.
Side Effects of Use of GH
A third of persons who take synthetic growth hormone will encounter negative side effects. Some examples are:
- fluid retention
- joint and muscle pain
- carpal tunnel syndrome
- high blood sugar levels
- high cholesterol levels
Conclusion
The pituitary gland produces GH, which promotes development in children and teenagers. It is also very significant in body composition, fluid balance, muscle and bone development, sugar and fat metabolism, and perhaps cardiac function. HGH is a synthetic hormone that is the active ingredient in various prescription medications and over-the-counter supplements.