Intrarenal Aki

Intrarenal acute kidney injury (AKI) is a sudden decline in kidney function caused by damage to the renal parenchyma, including the tubules, glomeruli, interstitium, or renal vasculature. Ischemia, nephrotoxic exposure, infection, or immune-mediated inflammation can injure these structures, reducing glomerular filtration and disrupting fluid, electrolyte, and waste regulation. In clinical practice, identifying intrarenal AKI requires integrating the patient’s history, medication and exposure profile, urinalysis, laboratory findings, and sometimes imaging or kidney biopsy. Accurate distinction from prerenal and postrenal causes guides treatment, supports prevention of further damage, and helps assess the risk of persistent kidney dysfunction.

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Research

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2026

Source: Gupta, K., et al. Intrarenal Injection of Escherichia coli in a Rat Model of Pyelonephritis. J. Vis. Exp. (2017).This video demonstrates the intrarenal injection of E. coli into the renal pelvis of an anesthetized rat to induce a localized kidney infection, modeling acute pyelonephritis. It highlights key surgical steps and aseptic techniques necessary for establishing a reproducible in vivo infection model for downstream analysis.

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This manuscript describes a rat surgical model of pyelonephritis using direct intra-renal infection by Escherichia coli into the renal pelvis. The experimental procedure can be utilized to study the pathogenesis of pyelonephritis as well as the associated inflammation and fibrosis.

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In this video, we demonstrate intra-renal drug administration in rats via the renal artery. This method is beneficial in improving drug targeting, drug potency, and minimizing systemic toxicity.

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In this video, we develop an orthotopic mouse model of renal cell carcinoma. This model results in reproducible primary tumors in the injected kidney and metastatic tumors in the lung, allowing the evaluation of disease progression and treatment.

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Cited by 23 •

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Implementation of an orthotopic model of renal cell carcinoma in immunocompetent mice affords the investigator a clinically-relevant system defined by the presence of a primary renal tumor and lung metastases in the same animal. This system can be used to preclinically test a variety of treatments in vivo.

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