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Heavy Metal Index

against arsenic-induced lung damage in rats

Source

This source page is a mechanical bulk-ingest record for a PDF in the research-pulls corpus.

Page snapshot
Cited by4 pages
Metals measured2
Evidence tierB
Year2025

Overview

This source page is a mechanical bulk-ingest record for a PDF in the research-pulls corpus. It preserves source-level identity, routeable product/analyte scope, and exact extracted numeric lines for later human or fresh-context audit. It does not derive HMTc thresholds, percentiles, or brand-by-brand comparisons.

Key numbers

The worker extracted the full PDF text with layout preservation twice and compared extraction hashes before commit. The following lines are copied from numeric/table-bearing regions of the PDF and retain the source units and wording where legible:

  • effects are closely tied to oxidative stress, apoptosis, and auto- tronic absorption spectra in the 200–1000 nm range in DMF
  • to signaling cascades such as the MAPK pathway, with ERKs Merck and had purities ranging from 99 to 99.9%. The nitrate
  • involved in the apoptosis and autophagy processes may offer water along with a typical rodent meal that included 17.48%
  • new opportunities for the treatment of lung diseases. Further- protein, 6.85% fat, 62.99% carbs, 4.08% ash, and 2.16%
  • sample size (n = 10) per group was determined based on
  • spectra were obtained in full scan range (m/z = 50–1000) under As2O3 (4 mg per kg body weight) for 4 weeks, then treated orally
  • elemental analysis and analytical results (Table S1) match the (DNA-Technology, Russia) using Maxima SYBR Green qPCR
  • metal : ligand ratio of 1 : 1 : 1 stoichiometry. and b-actin are represented in Table 1, The qPCR program was:
  • 2.4.3. Lung tissue preparation. To prepare 10% (w/v) tissue conformations aer conducting a thorough conformational
  • Table 1 Primers for qRT-PCR analysis
  • compounds (Fig. S2). Table 2 presents the typical electronic spectral data
  • 3.2.1. FT-IR analysis. Fig. S1 and Table S2 display the IR In the novel four complexes, the p–p* and n–p* transitions
  • intensity, suggesting that it did not participate in the chelation Cu(II) complexes with d9 conguration lie in the range of 1.7–2.2
  • carbonyl absorption frequencies, which were detected in all of conguration, exhibits meff value in a range of 3.88–4.3 BM.
  • Table 2 Distinctive electronic transitions, magnetic moments, and the resulting complex will be a system with three unpaired
  • of 3max are in parentheses and multiplied by 10−4 (mol−1 cm−1). b The PTP and Cu-Ni-PTP complexes, respectively, which means that
  • (100% base peak), 66.07 (31%), 77.95 (16%), 135.18 (8%), 167.27
  • (81.34%), 102.97 (66.25%), 252.60 (54.22%), 280.59 (78.12%), complex, while Fig. S12 depicts TGA for the remaining
  • mass spectral data were displayed in Table S3. nated H2O molecules, followed by a weight loss of 11.01% (calc.,
  • charge (m/z) range of 50–1000, using a Shimadzu GC-MS- accompanied by a loss of 25.67% (calc., 24.89%). In addition,
  • QP2010 Ultra instrument at 70 eV. The full MS range was the third stage was noticed at (290–367 °C) due to the loss of two
  • fragmentation proles that reect both the thiazole–phthalimide mental mass disappearance of 17.02% (calc., 15.48%). Finally,
  • apparent congestion of peaks with well-resolved m/z values range of (370–475 °C) with experimental weight loss of 30.71%
  • reects the fragmentation of multiple subunits instead of distinct (calc. 32.95%). The nal residual weight matched copper oxide
  • MS/MS isolation and identication of a subunit fragment. Major and cobalt oxide (calc. 15.49%). Table S4 showed the detailed
  • Table S3. For clarity, this methodological comment is now in the
  • that formed in the range of 7.82–6.98, which matched the linity of metal complexes. All-metal complexes in the 4–70 (q)
  • theoretical multiplet bands that developed in the 7.90– range were analyzed at 1.54 Å. Since solid frameworks are rarely
  • 7.31 ppm range. The interference of the various aromatic congured during the precipitation process, all X-ray diffraction
  • protons prevented the signals in this range from being resolved. curves (Fig. 2) demonstrate the somewhat amorphous nature of
  • Table 3 Powder XRD data for Cu-Co-PTP complex 6. Biological activity evaluation
  • measured values. Table 3 shows the observed and computed treated group compared to the control group (p < 0.001), sug-
  • Fig. 4 (A–D) Tissue biochemical parameters of Wistar rats exposed to As2O3 (4 mg per kg body weight). Data are presented as the means ± SE n
  • way ANOVA was used to analyze the data, and then the Tukey–Kramer multiple comparison test was used. Every value (n = 6) was shown as
  • mean ± SEM. a p < 0.05 in comparison to the control group; b p < 0.05 in comparison to the group that was treated with As2O3.
  • Table 4 Relative mRNA expression levels of BAX, ERK, Beclin1, and LC3, presented as fold-change (2−DDCT values)
  • and ERK by around 110% and 140% of the normal control
  • Co-PTP treated groups (by about 53% and 48% for As2O3-Cu-Zn-
  • PTP; 41% and 42% for As2O3-Cu-Ni-PTP; 37% and 35% for
  • chrome c, Caspase 9, and cleaved/active Caspase 3 were signif- (by approximately 67% and 49% for As2O3-Cu-Zn-PTP; 62% and
  • icantly downregulated during co-exposure to curcumin (2.5 mM) 44% for As2O3-Cu-Ni-PTP; 15% and 21% for As2O3-Cu-Co-PTP;
  • and 19% and 13% for As2O3-Cu-Ag-PTP, respectively), particu-

Methods (brief)

  • cellular dysfunction, and tissue damage, especially in the lungs. elemental analyses (C, H, and N). Atomic absorption was used
  • caspase activation leading to cell death.17 Apoptosis is also linked All the chemicals and solvents (HPLC grade) were acquired from
  • sample size (n = 10) per group was determined based on
  • As2O3 (4 mg per kg body weight) for 4 weeks, then treated orally for 15 min), the supernatant was collected and aliquoted in
  • the end of the experimental period, blood samples were the data, GraphPad Prism version 8 was utilized. A signicant
  • immediately collected from the retro-orbital venous plexus difference was considered as p < 0.05 for all tests.
  • atomic absorption and magnetic susceptibility. All complexes 1800 cm−1).43 This shi was ascribed to the relocation of an
  • Elemental analysis, atomic absorption, IR, UV-visible, and and the evaluated magnetic moment and molar conductivity
  • The experimental meff values for Cu-Co-PTP is 4.89 BM which conrming the suggested structures was mass spectrometry.

Implications

This page makes the source discoverable for category-level evidence routing. Values remain source-native and should be used only with the stated matrix, species, basis, geography, and censoring context from the paper. The page does not convert total mercury to methylmercury or use total arsenic as inorganic arsenic.

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Update history

The five most recent substantive edits to this page, classified major (evidence or structure moved), correction (a published value or statement was wrong and has been fixed), or minor (narrative rewritten without changing the underlying evidence). Each description is derived from what the edit did to this page; the linked commit is the authoritative record, routine regeneration passes are excluded, and the full version history lives in git. When DOI minting comes online (see schema docs), each entry below will also link to a version-pinned DataCite DOI.

CommitDateChangeDescription
b01ec52c2026-08-04major2 sections added
d49e450f2026-08-03major5 sections added; narrative text revised