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Hepatic and Pulmonary Vasoactive Response Triggered by Potentially Hazardous Chemicals After Passing Through the Gut Mucosa.

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Diagnostics (Basel, Switzerland) 2025 Vol.15(19)
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Dragoteanu M, Tolea Ș, Duca I, Mititelu R, Kairemo K

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: In a previous study, we observed significantly prolonged hepatic and pulmonary first-pass transit times (TTs) for Tc-pertechnetate absorbed through the colorectal mucosa during per-rectal portal sci

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APA Dragoteanu M, Tolea Ș, et al. (2025). Hepatic and Pulmonary Vasoactive Response Triggered by Potentially Hazardous Chemicals After Passing Through the Gut Mucosa.. Diagnostics (Basel, Switzerland), 15(19). https://doi.org/10.3390/diagnostics15192444
MLA Dragoteanu M, et al.. "Hepatic and Pulmonary Vasoactive Response Triggered by Potentially Hazardous Chemicals After Passing Through the Gut Mucosa.." Diagnostics (Basel, Switzerland), vol. 15, no. 19, 2025.
PMID 41095663

Abstract

: In a previous study, we observed significantly prolonged hepatic and pulmonary first-pass transit times (TTs) for Tc-pertechnetate absorbed through the colorectal mucosa during per-rectal portal scintigraphy (PRPS). This decrease in radiotracer flow velocity was not seen when Tc-pertechnetate was administered into the spleen during trans-splenic portal scintigraphy or injected intravenously in radionuclide angiocardiography. We hypothesized that Tc-pertechnetate, an artificial compound, is recognized during colorectal absorption as a potentially hazardous chemical (PHC), with its hepatic and pulmonary slowdown aiding elimination. A similar sudden decrease in portal flow occurs during early metastasis of colorectal cancer (CRC), as shown by a pathological rise in the hepatic perfusion index. We aimed to study the hepatic and pulmonary vasoactive responses triggered by PHCs after they pass through the gut mucosa and evaluate the potential activation of this mechanism in early CRC metastasis. : We measured transit times to determine whether hepatic and pulmonary vasoconstriction occur in response to radiotracers administered at different sites. We performed PRPS with in vivo Tc-labelled RBC to evaluate the liver transit time (LTT) and right heart to liver circulation time (RHLT). Liver angioscintigraphy (LAS) was used to assess RHLT following the intravenous injection of Tc-pertechnetate and Tc-HDP (hydroxyethylene-diphosphate). Lower rectum transmucosal dynamic scintigraphy (LR-TMDS) was conducted to measure RHLT of Tc-pertechnetate delivered into the lower rectum submucosa. LAS was performed to assess LTT for Tc-HDP intravenously injected and delivered to the gut mucosa via arterial flow. In healthy volunteers, PRPS showed notably increased LTT, ranging from 23.5 to 25.5 s, and RHLT (between 39.5 and 42.5 s) for in vivo Tc-labelled RBC. Significantly lower RHLT values ranging from 9 to 13.5 were observed for Tc-pertechnetate and Tc-HDP administered intravenously during LAS, as well as for Tc-pertechnetate at LR-TMDS (between 12 and 15 s). The LTT assessed at LAS for Tc-HDP ranged from 22 to 27 s. : An intense vasoconstriction occurs in the liver and lungs in response to substances recognized by the body as PHCs when they pass through the gut mucosa, aiding their elimination.