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Updated: Jan 24, 2026

An Effective Mouse Model of Unilateral Renal Ischemia-Reperfusion Injury
Published on: July 15, 2021
N,N-dimethyltryptamine Prevents Renal Ischemia-Reperfusion Injury in a Rat Model
Balázs Nemes1, Katalin Pető2, Norbert Németh2
1Department of Organ Transplantation, Institute of Surgery, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Background:
Ischemia reperfusion (I/R) injury remains one of the most challenging fields of organ transplantation. It is highly associated with the use of expanded criteria donors that might conclude to delayed graft function or early or late graft failure.
Objective:
To investigate the metabolic, microcirculatory parameters, and histologic changes under the effect of N,N-dimethyltryptamine (DMT) in a renal I/R model in rats.
Method:
In 26 anesthetized rats both kidneys were exposed. In the control group (n = 6) no other intervention happened. In 20 other animals, the right renal vessels were ligated, and after 60 minutes the right kidney was removed. The left renal vessels were clamped for 60 minutes then released, followed by 120 minutes of reperfusion. In the I/R group (n = 10), there was no additive treatment, while in I/R + DMT group (n = 10) DMT was administered 15 minutes before ischemia. Blood samples were taken, laser Doppler measurement was performed, and both kidneys were evaluated histologically.
Results:
Microcirculation (blood flux units [BFU]) diminished in all groups, but remarkably so in the I/R + DMT group. This group compensated better after the 30th minute of reperfusion. The control and I/R + DMT groups had similar BFUs after 120 minutes of reperfusion, but in the I/R group BFU was higher. Tubular necrosis developed in the I/R and I/R + DMT groups too; it was moderated under DMT effect, and severe without. Histologic injuries were less in I/R + DMT Group compared to non-treated animals.
Conclusion:
Histologic changes characteristic to I/R injuries were reversible and microcirculation recovered at the end of 120 minutes reperfusion under the administration of DMT. DMT can be used for renoprotection in kidney transplantation.
Insights
N,N-dimethyltryptamine (DMT) administration improved microcirculation and reduced kidney injury in a rat model of ischemia reperfusion (I/R). This suggests DMT may protect kidneys during transplantation by mitigating I/R damage.
Area of Science:
- Nephrology
- Transplantation immunology
- Pharmacology
Background:
- Ischemia reperfusion (I/R) injury is a major challenge in organ transplantation, particularly with expanded criteria donors.
- It can lead to delayed graft function or graft failure.
Purpose of the Study:
- To evaluate the effects of N,N-dimethyltryptamine (DMT) on metabolic, microcirculatory, and histologic parameters in a rat renal I/R model.
Main Methods:
- Rats underwent renal I/R, with some receiving DMT 15 minutes before ischemia.
- Microcirculation was assessed using laser Doppler, and kidneys were examined histologically.
Main Results:
- DMT administration improved microcirculation recovery and reduced tubular necrosis and overall histologic injury compared to untreated I/R rats.
- Kidney microcirculation in the DMT-treated group recovered to levels similar to controls.
Conclusions:
- Histologic damage from renal I/R injury is reversible with DMT administration.
- DMT demonstrates renoprotective potential, suggesting its utility in kidney transplantation to mitigate I/R injury.
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