# Cerebral Inflammation in an Animal Ischemia–Reperfusion Model Comparing Histidine-Tryptophan-α-Ketoglutarate and Del Nido Cardioplegia

**Authors:** Kristin Klaeske, Maja-Theresa Dieterlen, Jagdip Kang, Zoe Detzer, André Ginther, Susann Ossmann, Michael A. Borger, Philipp Kiefer, Alexandro A. Hoyer

PMC · DOI: 10.3390/life15030451 · Life · 2025-03-13

## TL;DR

This study compares two heart surgery solutions, HTK and del Nido, and finds del Nido may be safer for the brain by reducing inflammation.

## Contribution

The study provides new evidence on the comparative safety of del Nido cardioplegia over HTK in reducing cerebral inflammation.

## Key findings

- HTK cardioplegia caused significant electrolyte imbalances compared to del Nido.
- Del Nido showed lower IL-1β mRNA expression in brain regions compared to HTK.
- Del Nido cardioplegia is proposed as a safer alternative for cerebral inflammation.

## Abstract

Brain injury and cerebral inflammation are frequent complications following cardiopulmonary bypass (CPB) resulting in neurocognitive dysfunction, encephalopathy, or stroke. We compared cerebral inflammation induced by del Nido and histidine-tryptophan-α-ketoglutarate (HTK) cardioplegia in a porcine model. Pigs underwent 90 min cardiac arrest using HTK (n = 9) or Jonosteril®-based del Nido cardioplegia (n = 9), followed by a 120 min reperfusion. Brain biopsies were collected and analyzed for the mRNA and protein expression of hypoxia-inducible factor-1α (HIF-1α) and cytokines. HTK induced a decrease in blood sodium, chloride, and calcium concentration (cross-clamp aorta: psodium < 0.01, pchloride < 0.01, pcalcium < 0.01; 90 min ischemia: psodium < 0.01, pchloride < 0.01, pcalcium = 0.03) compared to the more stable physiological electrolyte concentrations during del Nido cardioplegia. Hyponatremia and hypochloremia persisted after a 120 min reperfusion in the HTK group (psodium < 0.01, pchloride = 0.04). Compared to del Nido, a higher mRNA expression of the proinflammatory cytokine IL-1β was detected in the frontal cortex (HTK: ∆Ct 6.5 ± 1.7; del Nido: ∆Ct 8.8 ± 1.5, p = 0.01) and the brain stem (HTK: ∆Ct 5.7 ± 1.5; del Nido: ∆Ct 7.5 ± 1.6, p = 0.02) of the HTK group. In conclusion, we showed comparability of HTK and del Nido for cerebral inflammation except for IL-1β expression. Based on our study results, we conclude that del Nido cardioplegia is a suitable and safe alternative to the conventional HTK solution.

## Linked entities

- **Genes:** HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091], IL1B (interleukin 1 beta) [NCBI Gene 3553]

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 397122] {aka IL1B1}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 396696]
- **Diseases:** Cerebral Inflammation (MESH:D007249), Hyponatremia (MESH:D007010), encephalopathy (MESH:D001927), Brain injury (MESH:D001930), Ischemia (MESH:D007511), stroke (MESH:D020521), neurocognitive dysfunction (MESH:D019965), cardiac arrest (MESH:D006323)
- **Species:** Sus scrofa (pig, species) [taxon 9823]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11943810/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11943810/full.md

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Source: https://tomesphere.com/paper/PMC11943810