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Sulfate-modified nanosized polystyrene impairs memory by inhibiting ionotropic glutamate receptors and the cAMP-response element binding protein (CREB) pathway in Caenorhabditis elegans

The Science of The Total Environment 2023 7 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 50 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Pei-Ling Yen, Ting‐An Lin, Pei-Ling Yen, Vivian Hsiu‐Chuan Liao Ting‐An Lin, Pei-Ling Yen, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Chun Ming How, Pei-Ling Yen, Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao Pei-Ling Yen, Ting‐An Lin, Ting‐An Lin, Ting‐An Lin, Vivian Hsiu‐Chuan Liao Ting‐An Lin, Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao Vivian Hsiu‐Chuan Liao

Summary

Researchers found that sulfate-modified polystyrene nanoplastics impair both short- and long-term associative memory in C. elegans by downregulating ionotropic glutamate receptors and the CREB signaling pathway — conserved molecular mechanisms that also underlie learning and memory in mammals — raising concerns about nanoplastic effects on cognition.

Nanoplastic contamination is an emerging environmental concern worldwide. In particular, sulfate anionic surfactants often appear along with nanosized plastic particles in personal care products, suggesting that sulfate-modified nanosized polystyrene (S-NP) may occur, remain, and spread into the environment. However, whether S-NP adversely affects learning and memory is unknown. In this study, we used a positive butanone training protocol to evaluate the effects of S-NP exposure on short-term associative memory (STAM) and long-term associative memory (LTAM) in Caenorhabditis elegans. We observed that long-term S-NP exposure impairs both STAM and LTAM in C. elegans. We also observed that mutations in the glr-1, nmr-1, acy-1, unc-43, and crh-1 genes eliminated the STAM and LTAM impairment induced by S-NP, and the mRNA levels of these genes were also decreased upon S-NP exposure. These genes encode ionotropic glutamate receptors (iGluRs), cyclic adenosine monophosphate (cAMP)/Ca signaling proteins, and cAMP-response element binding protein (CREB)/CRH-1 signaling proteins. Moreover, S-NP exposure inhibited the expression of the CREB-dependent LTAM genes nid-1, ptr-15, and unc-86. Our findings provide new insights into long-term S-NP exposure and the impairment of STAM and LTAM, which involve the highly conserved iGluRs and CRH-1/CREB signaling pathways.

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