# Combination of dasatinib and quercetin improves cognitive abilities in aged male Wistar rats, alleviates inflammation and changes hippocampal synaptic plasticity and histone H3 methylation profile

**Authors:** Adam Krzystyniak, Malgorzata Wesierska, Gregory Petrazzo, Agnieszka Gadecka, Magdalena Dudkowska, Anna Bielak-Zmijewska, Grazyna Mosieniak, Izabela Figiel, Jakub Wlodarczyk, Ewa Sikora

PMC · DOI: 10.18632/aging.203835 · Aging (Albany NY) · 2022-01-18

## TL;DR

Treating aged rats with dasatinib and quercetin improved their memory and reduced inflammation, possibly by altering brain cell structure and gene regulation.

## Contribution

This study shows that D+Q improves cognition in aged rats by affecting hippocampal spine morphology and histone methylation.

## Key findings

- D+Q treatment improved learning and memory in aged rats.
- D+Q reduced peripheral inflammation and senescent cell secretome markers.
- D+Q altered hippocampal dendritic spine morphology and histone H3 methylation.

## Abstract

Aging is associated with cognitive decline and accumulation of senescent cells in various tissues and organs. Senolytic agents such as dasatinib and quercetin (D+Q) in combination have been shown to target senescent cells and ameliorate symptoms of aging-related disorders in mouse models. However, the mechanisms by which senolytics improve cognitive impairments have not been fully elucidated particularly in species other than mice. To study the effect of senolytics on aging-related multifactorial cognitive dysfunctions we tested the spatial memory of male Wistar rats in an active allothetic place avoidance task. Here we report that 8 weeks treatment with D+Q alleviated learning deficits and memory impairment observed in aged animals. Furthermore, treatment with D+Q resulted in a reduction of the peripheral inflammation measured by the levels of serum inflammatory mediators (including members of senescent cell secretome) in aged rats. Significant improvements in cognitive abilities observed in aged rats upon treatment with D+Q were associated with changes in the dendritic spine morphology of the apical dendritic tree from the hippocampal CA1 neurons and changes in the level of histone H3 trimethylation at lysine 9 and 27 in the hippocampus. The beneficial effects of D+Q on learning and memory in aged rats were long-lasting and persisted at least 5 weeks after the cessation of the drugs administration. Our results expand and provide new insights to the existing knowledge associated with effects of senolytics on alleviating age-related associated cognitive dysfunctions.

## Linked entities

- **Chemicals:** dasatinib (PubChem CID 3062316), quercetin (PubChem CID 5280343)

## Full-text entities

- **Genes:** Suv39h1 (suppressor of variegation 3-9 1) [NCBI Gene 20937] {aka DXHXS7466e, H3-K9-HMTase 1, KMT1A, mIS6}, CX3CL1 (C-X3-C motif chemokine ligand 1) [NCBI Gene 6376] {aka ABCD-3, C3Xkine, CXC3, CXC3C, NTN, NTT}, CCL11 (C-C motif chemokine ligand 11) [NCBI Gene 6356] {aka SCYA11}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, Il4 (interleukin 4) [NCBI Gene 287287] {aka Il4e12}, Il2 (interleukin 2) [NCBI Gene 116562], CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, Cyp2b10 (cytochrome P450, family 2, subfamily b, polypeptide 10) [NCBI Gene 13088] {aka Cyp2b, Cyp2b20, p16}, IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, Gfap (glial fibrillary acidic protein) [NCBI Gene 24387], Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 24770] {aka MCP-1, MCP1, Scya2, Sigje}, Dlg4 (discs large MAGUK scaffold protein 4) [NCBI Gene 13385] {aka Dlgh4, PSD-95, PSD95, SAP90, SAP90A}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, App (amyloid beta precursor protein) [NCBI Gene 54226] {aka Abeta}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Rbfox3 (RNA binding fox-1 homolog 3) [NCBI Gene 287847] {aka Hrnbp3, Neun, RGD1560070}, CCL5 (C-C motif chemokine ligand 5) [NCBI Gene 6352] {aka D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228}, Asprv1 (aspartic peptidase, retroviral-like 1) [NCBI Gene 67855] {aka 2300003P22Rik, SASP, SASPase, Taps}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, CXCL2 (C-X-C motif chemokine ligand 2) [NCBI Gene 2920] {aka CINC-2a, GRO2, GROb, MGSA-b, MIP-2a, MIP2}, CXCL5 (C-X-C motif chemokine ligand 5) [NCBI Gene 6374] {aka ENA-78, SCYB5}, CCL3 (C-C motif chemokine ligand 3) [NCBI Gene 6348] {aka G0S19-1, LD78, LD78ALPHA, MIP-1-alpha, MIP1A, SCI}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, H2bc1 (H2B clustered histone 1) [NCBI Gene 24829] {aka Hist1h2ba, Th2b, histone}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, Bdnf (brain derived neurotrophic factor) [NCBI Gene 12064], CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, Syp (synaptophysin) [NCBI Gene 20977] {aka A230093K24Rik, Syn, p38}, Il1a (interleukin 1 alpha) [NCBI Gene 24493] {aka IL-1 alpha, IL-1F1}, H3c7 (H3 clustered histone 7) [NCBI Gene 260423] {aka H3.2-221, H3c13, H3c14, H3c15, H3c2, H3c3}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, Il10 (interleukin 10) [NCBI Gene 25325] {aka IL10X, If2a}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, CXCL10 (C-X-C motif chemokine ligand 10) [NCBI Gene 3627] {aka C7, IFI10, INP10, IP-10, SCYB10, crg-2}, Hist1h3b (histone cluster 1, H3b) [NCBI Gene 680498], Cdkn1a (cyclin dependent kinase inhibitor 1A) [NCBI Gene 12575] {aka CAP20, CDKI, CIP1, Cdkn1, P21, SDI1}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, IL18 (interleukin 18) [NCBI Gene 3606] {aka IGIF, IL-18, IL-1g, IL1F4}, Glb1 (galactosidase, beta 1) [NCBI Gene 316033], IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** inflammation (MESH:D007249), shock (MESH:D012769), dementia (MESH:D003704), geriatric syndromes (MESH:D013577), Parkinson's and Alzheimer's diseases (MESH:D010300), COVID-19 infection (MESH:D000086382), cancer (MESH:D009369), age-related disorders (MESH:D008569), diabetes (MESH:D003920), AAPAT (MESH:D000092442), learning and memory deficits (MESH:D007859), aging-associated diseases (MESH:C564653), anxiety symptoms (MESH:D001008), gliosis (MESH:D005911), neurodegeneration (MESH:D019636), tau (MESH:C536599), NFT (MESH:D055956), cognitive behavioral deficits (MESH:D003072), cardiovascular disease (MESH:D002318), AD (MESH:D000544), neuroinflammation (MESH:D000090862), degeneration of neurons (MESH:D009410)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** P301L
- **Cell lines:** BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC8833137/full.md

## References

52 references — full list in the complete paper: https://tomesphere.com/paper/PMC8833137/full.md

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Source: https://tomesphere.com/paper/PMC8833137