Remote ischemic conditioning in a rat model of testicular torsion: does it offer testicular protection?

• Published in: Journal of pediatric urology Vol. 15; no. 1; pp. 43.e1 - 43.e7
• Main Authors: Mansour, M., Degheili, J., Khalifeh, I., Tamim, H., Jaafar, R.F., El-Hout, Y.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01-02-2019
• Subjects: Animals; Disease Models, Animal; Ischemia - etiology; Ischemia - prevention & control; Ischemic Preconditioning - methods; Male; Rat; Rats; Rats, Sprague-Dawley; Remote ischemic conditioning; Reperfusion Injury - etiology; Reperfusion Injury - prevention & control; Spermatic Cord Torsion - complications; Testicular torsion; Testis; Testis - blood supply; Testis; Testicular torsion; Remote ischemic conditioning; Rat
• ISSN: 1477-5131; 1873-4898
• DOI: 10.1016/j.jpurol.2018.09.012

Testicular torsion is a surgical emergency mainly affecting adolescent boys, with a relatively high rate of missed torsion and testicular loss secondary to delay in prompt diagnosis and surgical intervention. With ischemic reperfusion injury as its underlying culprit, testicular torsion may respond favorably to remote ischemic conditioning (RIC) where a non-privileged site (e.g. limb) is concurrently rendered ischemic to divert the cascade of reperfusion injury from the privileged organ (e.g. testicle), thus offering a protective effect in improving salvage. This mechanism is established for other organs, whereas it has not been evaluated for testis.
It was aimed to evaluate RIC in a rat model of testicular torsion as a proof of principle that, similar to what has been demonstrated in other organs, RIC does offer testicular protection.
This is an animal experimental study. Thirty Sprague–Dawley male rats were divided into control group (n = 15) and experimental group (n = 15). Non-survival surgeries of right-sided spermatic cord torsion (720° counter-clockwise twist) were performed for both the groups (45 min) followed by detorsion and reperfusion (5 min) and then orchiectomy. For the experiment group, an intervention of tail clamping to create RIC was applied 5 min after torsion, then unclamping 5 min before detorsion, followed by detorsion and reperfusion for 5 min and then orchiectomy. The testicles were histologically and immunologically examined using a hypoxia inducible factor (HIF-1α) ELISA Kit. The histological findings on ischemic changes, vascular congestion, and immunohistochemistry were quantified using previously described, validated grading systems.
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This is the first study to demonstrate the concept of RIC in an animal model of testicular torsion. It is limited by the non-availability of similar studies to compare outcomes and by the caution of extrapolating animal studies on humans. It does lay grounds, however, to subsequent studies to further elaborate on this concept and its clinical applicability.
When RIC is applied in the experimental setting of testicular torsion, there is less evidence of hypoxic injury by histology and immunohistochemistry.