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portada Arginase Enzyme in Iraqi Acromegaly Patients: Biochemical Insights
Type
Physical Book
Author
Publisher
Language
Inglés
Pages
80
Format
Paperback
Dimensions
22.9 x 15.2 x 0.5 cm
Weight
0.13 kg.
ISBN13
9786207461806
Categories

Arginase Enzyme in Iraqi Acromegaly Patients: Biochemical Insights

Fatima Kh Malek (Author) · Salma A. Abbas (Author) · Baydaa A. Abed (Author) · LAP Lambert Academic Publishing · Paperback

Arginase Enzyme in Iraqi Acromegaly Patients: Biochemical Insights - Malek, Fatima Kh ; Abbas, Salma A. ; Abed, Baydaa A.

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Synopsis "Arginase Enzyme in Iraqi Acromegaly Patients: Biochemical Insights"

L-arginase (EC 3.5.3.1), the final enzyme in the urea cycle, is a binuclear Mn2+ metalloenzyme. The enzyme catalyzes a reaction involving the hydrolysis of L-arginine to L-ornithine and urea. Acromegaly (ACRO) is a rare and complex hormonal syndrome classified as a chronic disorder characterized by elevated growth hormone (GH) and, consequently, insulin-like growth factor-1 (IGF-1). This is commonly caused by a GH-secreting pituitary adenoma, leading to multisystem impacts. These impacts affect the osteoarticular system, muscles, brain, heart and blood vessels, respiratory and hematopoietic system, kidneys, liver and pancreas, thyroid, adipose tissue, and metabolic system. The objective of this study is to evaluate the levels of arginase activity, GH, IGF-1, glucose, lipid profile, and serum urea in ACRO patients with and without diabetes. Additionally, the study aims to explore the correlation between Arginase and GH, glucose, and lipid profile.

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