The cause of renal damage caused by methacrylate propanamide is related to the failure of clinical doctors to strictly grasp the indications for drug use. Patients with renal artery stenosis, renal artery thrombosis, solitary kidney, and excessive dosage of methacrylate propanamide are all prone to increase the risk of renal damage. The pathogenesis of renal damage caused by methacrylate propanamide may have the following aspects:
1, Changes in hemodynamics
Angiotensin II within the kidney can affect renal vascular tone, causing constriction of the afferent and efferent arterioles, leading to reduced renal blood flow, ensuring blood volume and maintaining blood pressure. Methacrylate propanamide blocks the formation of angiotensin II, reducing its effect. Compared with the afferent arteriole, the resistance of the efferent arteriole is reduced more significantly, resulting in reduced glomerular blood flow and decreased glomerular filtration rate, causing renal function damage. When there is renal artery stenosis, the glomerular blood flow decreases, and its glomerular filtration rate depends on the constriction of the efferent arteriole to maintain. After the use of methacrylate propanamide, the efferent arteriole is dilated, leading to a sudden decrease in glomerular filtration rate and causing acute renal failure.
2, The direct toxic effect of methacrylate propanamide on the proximal tubular epithelial cells
It may be related to the fact that methacrylate propanamide blocks the function of some key esterase in the proximal tubular epithelial cells, or methacrylate propanamide may hinder the recovery of cells after ischemia, aggravate cellular damage after reperfusion, and thus lead to acute tubular necrosis.
3, Allergic factors and immune regulatory function disorder
It may be related to the post-drug allergic reaction, which causes infiltration of monocytes and lymphocytes in the renal interstitium and the release of some cytokines (such as interleukin-1, interleukin-2, tumor necrosis factor-α).