Proteomics

Dataset Information

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Quantification of glycated rat serum albumin peptides


ABSTRACT: Serum albumin is the most abundant plasma protein with a large number of lysine and arginine residues. Hence, it is highly susceptible to glycation, a non-enzymatic reaction involving binding of non-reducing sugars to proteins, in vivo. Oxidative stress is known to promote glycation and the Advanced glycation end products (AGEs) formed through glycation bind to their cell-surface receptor (RAGE). AGE-RAGE interaction activates downstream intracellular signaling pathways resulting in increased inflammation and oxidative stress and the vicious cycle of Oxidative stress and AGE formation continues. Here we quantified glycated albumin peptides mass spectrometrically in maternally separated rats and compared their levels with those in Control to investigte if AGE accumulation is associated with the increased inflammation and oxidative stress in MS rats.

INSTRUMENT(S):

ORGANISM(S): Rattus Norvegicus (rat)

TISSUE(S): Blood Serum

SUBMITTER: Arvindkumar Chaurasiya  

LAB HEAD: Mahesh J Kulkarni

PROVIDER: PXD074495 | Pride | 2026-06-29

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
Control_SWATH.zip Other
MS_SWATH.zip Other
SWATH_result.txt Txt
Skyline_Result.sky Other
Skyline_Result.sky.view Other
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Publications

A history of maternal separation drives systemic aging-associated signatures in middle-aged male rats.

Chaudhari Pratik R PR   Chaurasiya Arvindkumar H AH   Vaidya Ashok D B ADB   Kulkarni Mahesh J MJ   Vaidya Vidita A VA  

Frontiers in cellular neuroscience 20260504


Early adversity programs induce changes that can accelerate biological aging. Using the early stress model of maternal separation (MS), we assessed oxidative, metabolic, and biochemical consequences in serum derived from middle-aged male rats to investigate systemic correlates of physiological aging in MS animals. We noted significant increases in serum corticosterone in middle-aged MS male rats, accompanied by reduced serum levels of trophic factors, brain-derived neurotrophic factor (BDNF), an  ...[more]

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