# Improvement of Cardiac Function by Polyclonal Antibodies Against Ca2+/Mg2+ ecto-ATPase in Hearts Subjected to Ischemia-Reperfusion

**Authors:** Naranjan S. Dhalla, Vijayan Elimban, Petr Ostadal

PMC · DOI: 10.3390/ijms27042002 · International Journal of Molecular Sciences · 2026-02-19

## TL;DR

This study shows that antibodies against a specific enzyme can improve heart function after injury by reducing calcium overload.

## Contribution

The novel finding is that inhibiting Ca2+/Mg2+ ecto-ATPase with antibodies improves recovery after heart injury.

## Key findings

- Pretreatment with antibodies improved recovery of cardiac function after ischemia-reperfusion injury.
- Antibodies reduced Ca2+/Mg2+ ecto-ATPase activity and attenuated intracellular calcium overload.
- Treatment with antibodies decreased ATP-induced calcium increases in heart cells.

## Abstract

Delayed reperfusion of an ischemic heart is known to impair the recovery of cardiac function, and the occurrence of intracellular Ca2+ overload in the myocardium is considered to play a critical role in the development of ischemia-reperfusion (I/R) injury. Since Ca2+/Mg2+ ecto-ATPase, which is activated by millimolar concentrations of Ca2+ or Mg2+, has been shown to serve as a Ca2+ gating mechanism for the entry of Ca2+ and subsequent development of intracellular Ca2+ overload, we investigated the role of depression in Ca2+/Mg2+ ecto-ATPase activity by polyclonal antibodies against Ca2+/Mg2+ ecto-ATPase in promoting the recovery of cardiac function in isolated perfused rat hearts upon subjection to I/R injury. Incubation of sarcolemma (SL) membranes with immune serum or purified IgG antibody fraction was found to depress both Ca2+-ATPase and Mg2+-ATPase activities. Pretreatment of hearts with immune serum or purified antibodies was observed to improve the recovery of cardiac function and depress the SL Ca2+/Mg2+ ecto-ATPase activities in hearts subjected to I/R injury. A marked increase in myocardial Ca2+ content in I/R hearts was also attenuated by immune serum treatment. Furthermore, treatment of cardiomyocytes from normal hearts with immune serum or purified antibodies reduced the ATP-induced increase in intracellular Ca2+ concentration. These results suggest that improvement in the recovery of cardiac function in hearts subjected to I/R injury by polyclonal Ca2+/Mg2+ ecto-ATPase antibodies may be due to the attenuation of intracellular Ca2+ overload.

## Linked entities

- **Chemicals:** Ca2+ (PubChem CID 271), Mg2+ (PubChem CID 888), ATP (PubChem CID 5957)
- **Diseases:** ischemia-reperfusion injury (MONDO:0005203)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Ceacam1 (CEA cell adhesion molecule 1) [NCBI Gene 81613] {aka BGPR, Bgp, CD66a, Ccam1}, F2r (coagulation factor II (thrombin) receptor) [NCBI Gene 25439] {aka Par1, TRGPC}, Edn1 (endothelin 1) [NCBI Gene 24323] {aka Et1}, Uts2r (urotensin 2 receptor) [NCBI Gene 57305] {aka Gpr14, Senr, UR-2-R}
- **Diseases:** Ischemia (MESH:D007511), depression (MESH:D003866), LVDP (MESH:D018487), cardiac complications (MESH:D006331), myocardial cell damage (MESH:D009202), ischemic (MESH:D002545), ischemic heart (MESH:D017202), ischemic myocardium (MESH:D017682), /R (MESH:C580424), myocardial infarction (MESH:D009203), cardiovascular diseases (MESH:D002318), thrombotic disease (MESH:D013927), I/R (MESH:D015427), injury to (MESH:D014947), mitochondrial defects (MESH:C565376)
- **Chemicals:** verapamil (MESH:D014700), pyridoxal 5'- phosphate (MESH:D011732), KCl (MESH:D011189), hydroxyl radicals (MESH:D017665), LiBr (MESH:C040949), carbon dioxide (MESH:D002245), Fura 2-AM (MESH:C049925), ATP (MESH:D000255), Bay-K 8644 (MESH:D001498), sucrose (MESH:D013395), xylazine (MESH:D014991), H2O2 (MESH:D006861), superoxide (MESH:D013481), Ca2+ (-), Na+ (MESH:D012964), oxygen (MESH:D010100), Pi (MESH:D010716), inorganic phosphate (MESH:D010710)
- **Species:** Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

85 references — full list in the complete paper: https://tomesphere.com/paper/PMC12941162/full.md

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Source: https://tomesphere.com/paper/PMC12941162