# Increased rubidium levels in brain regions involved in food intake in obese rats

**Authors:** Magdalena Szczerbowska-Boruchowska, Aleksandra Chenczke, Blazej Ruszczycki, Pawel Wrobel, Wiktoria Tokarczyk, Patryk Stec, Katarzyna M. Sowa, Agata Ziomber-Lisiak

PMC · DOI: 10.1007/s00429-025-02930-8 · Brain Structure & Function · 2025-05-15

## TL;DR

Obese rats have higher rubidium levels in brain regions linked to appetite regulation, suggesting a possible connection between rubidium and obesity.

## Contribution

This study is the first to show that rubidium levels are significantly elevated in brain areas involved in appetite regulation in obese rats.

## Key findings

- Rubidium levels were significantly higher in all brain regions examined in obese rats.
- The largest relative increase in rubidium was observed in the orbitofrontal cortex.
- Rubidium was the only element distinguishing obese rats in all examined brain structures.

## Abstract

The hypothalamus, particularly its ventromedial and lateral regions, plays a pivotal role in homeostatic appetite regulation and is therefore a significant brain structure in the development of obesity. Additionally, the development of obesity can be caused by improper hedonic regulation, which involves neural circuits and systems associated with pleasure and reward. Several studies indicate a possible link between rubidium (Rb) and obesity, despite this element is not being typically considered influential in vital life processes. The present study, therefore, aims to investigate whether excessive body fat in obese animals alters rubidium levels in brain regions directly or indirectly involved in appetite regulation. The research was conducted on high-calorie diet (HCD)-induced obese rats (OB, n = 8) and their lean counterparts (L, n = 8). The determination of Rb levels in brain areas was performed using synchrotron radiation-based X-ray fluorescence microanalysis (SRXRF). The obtained results show a significantly higher level of Rb in all brain areas examined, although the increase in this element in obese individuals was not the same in all structures. The largest relative difference (over 70%) was observed for the orbitofrontal cortex, and the smallest (about 35%) for the amygdala. Principal component analysis with linear projections demonstrated a clear differentiation between the brain structures of obese and non-obese individuals based on the full elemental composition of tissues, while Rb was the only element that distinguished the obese group in each of the examined brain structures. The results obtained clearly confirm the increase in Rb levels in the brain structures responsible for regulating appetite in obesity.

## Linked entities

- **Chemicals:** rubidium (PubChem CID 105153)
- **Diseases:** obesity (MONDO:0011122)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Pcsk2 (proprotein convertase subtilisin/kexin type 2) [NCBI Gene 25121], insulin [NCBI Gene 108634241], Siglec1 (sialic acid binding Ig like lectin 1) [NCBI Gene 311426] {aka Sn}, Pcsk1 (proprotein convertase subtilisin/kexin type 1) [NCBI Gene 25204] {aka BDP, PC1, PC3}, Nol3 (nucleolar protein 3) [NCBI Gene 85383] {aka Arc}, CRP [NCBI Gene 102189259]
- **Diseases:** growth retardation (MESH:D006130), cardiovascular diseases (MESH:D002318), aggression (MESH:D010554), type 2 diabetes (MESH:D003924), OB (MESH:D009765), undernutrition (MESH:D044342), miscarriage (MESH:D000022), addiction (MESH:D019966), neuronal damage (MESH:D009410), overeating (MESH:D006963), sodium-potassium pump dysfunction (MESH:C566111), HCD (MESH:D011502), metabolic (MESH:D008659), metabolic syndrome (MESH:D024821), overnutrition (MESH:D044343), impaired brain function (MESH:D001927), inflammation (MESH:D007249), Rb deficiency (MESH:D007153), neurodegenerative diseases (MESH:D019636), K deficiency (MESH:D014813), AD (MESH:D000544)
- **Chemicals:** triglycerides (MESH:D014280), Ca (MESH:D002118), Br (MESH:D001966), sodium (MESH:D012964), P (MESH:D010758), B4C (-), Cu (MESH:D003300), lipid (MESH:D008055), Mo (MESH:D008982), Zn (MESH:D015032), Cl (MESH:D002713), DA (MESH:D004298), K (MESH:D011188), estradiol (MESH:D004958), ROS (MESH:D017382), 3,4-methylenedioxyamphetamine (MESH:D015104), Mn (MESH:D008345), S (MESH:D013455), Fe (MESH:D007501), sugars (MESH:D000073893), alpha-tocopherol (MESH:D024502), glucose (MESH:D005947), progesterone (MESH:D011374), Rb (MESH:D012413), cholesterol (MESH:D002784)
- **Species:** Macaca mulatta (rhesus macaque, species) [taxon 9544], Capra hircus (domestic goat, species) [taxon 9925], Homo sapiens (human, species) [taxon 9606], Macaca (macaque, genus) [taxon 9539], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

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Source: https://tomesphere.com/paper/PMC12081528