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(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model
Malaria, a mosquito-borne disease caused by Plasmodium spp. is considered to be a global threat, specifically for the developing countries. In human subjects considerable information exists regarding post-malarial physiology. However, most murine malarial models are lethal, and most studies deal wit...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691208/ https://www.ncbi.nlm.nih.gov/pubmed/23826178 http://dx.doi.org/10.1371/journal.pone.0066954 |
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author | Sengupta, Arjun Ghosh, Soumita Sharma, Shobhona Sonawat, Haripalsingh M. |
author_facet | Sengupta, Arjun Ghosh, Soumita Sharma, Shobhona Sonawat, Haripalsingh M. |
author_sort | Sengupta, Arjun |
collection | PubMed |
description | Malaria, a mosquito-borne disease caused by Plasmodium spp. is considered to be a global threat, specifically for the developing countries. In human subjects considerable information exists regarding post-malarial physiology. However, most murine malarial models are lethal, and most studies deal with acute phases occurring as disease progresses. Much less is known regarding physiological status post-parasite clearance. We have assessed the physiological changes at the organ levels using (1)H NMR based metabonomics in a non lethal self-clearing murine malarial model of P. chabaudi parasites and Balb/C, far beyond the parasite clearance point. The results showed distinct metabolic states between uninfected and infected mice at the peak parasitemia, as well as three weeks post-parasite clearance. Our data also suggests that the response at the peak infection as well as recovery exhibited distinct sexual dimorphism. Specifically, we observed accumulation of acetylcholine in the brain metabolic profile of both the sexes. This might have important implication in understanding the pathophysiology of the post malarial neurological syndromes. In addition, the female liver showed high levels of glucose, dimethylglycine, methylacetoacetate and histidine after three weeks post-parasite clearance, while the males showed accumulation of branched chain amino acids, lysine, glutamine and bile acids. |
format | Online Article Text |
id | pubmed-3691208 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36912082013-07-03 (1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model Sengupta, Arjun Ghosh, Soumita Sharma, Shobhona Sonawat, Haripalsingh M. PLoS One Research Article Malaria, a mosquito-borne disease caused by Plasmodium spp. is considered to be a global threat, specifically for the developing countries. In human subjects considerable information exists regarding post-malarial physiology. However, most murine malarial models are lethal, and most studies deal with acute phases occurring as disease progresses. Much less is known regarding physiological status post-parasite clearance. We have assessed the physiological changes at the organ levels using (1)H NMR based metabonomics in a non lethal self-clearing murine malarial model of P. chabaudi parasites and Balb/C, far beyond the parasite clearance point. The results showed distinct metabolic states between uninfected and infected mice at the peak parasitemia, as well as three weeks post-parasite clearance. Our data also suggests that the response at the peak infection as well as recovery exhibited distinct sexual dimorphism. Specifically, we observed accumulation of acetylcholine in the brain metabolic profile of both the sexes. This might have important implication in understanding the pathophysiology of the post malarial neurological syndromes. In addition, the female liver showed high levels of glucose, dimethylglycine, methylacetoacetate and histidine after three weeks post-parasite clearance, while the males showed accumulation of branched chain amino acids, lysine, glutamine and bile acids. Public Library of Science 2013-06-24 /pmc/articles/PMC3691208/ /pubmed/23826178 http://dx.doi.org/10.1371/journal.pone.0066954 Text en © 2013 Sengupta et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sengupta, Arjun Ghosh, Soumita Sharma, Shobhona Sonawat, Haripalsingh M. (1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title |
(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title_full |
(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title_fullStr |
(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title_full_unstemmed |
(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title_short |
(1)H NMR Metabonomics Indicates Continued Metabolic Changes and Sexual Dimorphism Post-Parasite Clearance in Self-Limiting Murine Malaria Model |
title_sort | (1)h nmr metabonomics indicates continued metabolic changes and sexual dimorphism post-parasite clearance in self-limiting murine malaria model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691208/ https://www.ncbi.nlm.nih.gov/pubmed/23826178 http://dx.doi.org/10.1371/journal.pone.0066954 |
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