Mutations in the HGPRT1 gene, which encodes hypoxanthine-guanine phosphoribosyltransferase (HGprt), housekeeping enzyme responsible for recycling purines, lead to Lesch-Nyhan disease (LND). Clinical expression of LND indicates that HGprt deficiency has adverse effects on gastrointestinal motility. Therefore, we aimed to evaluate intestinal motility in HGprt knockout mice (HGprt). Spontaneous and neurally evoked mechanical activity was recorded in vitro as changes in isometric tension in circular muscle strips of distal colon. HGprt tissues showed a lower in amplitude spontaneous activity and atropine-sensitivity neural contraction compared to control mice. The responses to carbachol and to high KCl were reduced, demonstrating a widespread impairment of contractility. L-NAME was not able in the HGprt tissues to restore the large amplitude contractile activity typical of control. In HGprt colon, a reduced expression of dopaminergic D1 receptor was observed together with the loss of its tonic inhibitory activity present in control-mice. The analysis of inflammatory and oxidative stress in colonic tissue of HGprt mice revealed a significant increase of lipid peroxidation associated with over production of oxygen free radicals. In conclusion, HGprt deficiency in mice is associated with a decrease in colon contractility, not dependent upon reduction of acetylcholine release from the myenteric plexus or hyperactivity of inhibitory signalling. By contrast the increased levels of oxidative stress could partially explain the reduced colon motility in HGprt mice. Colonic dysmotility observed in HGprt mice may mimic the gastrointestinal dysfunctions symptoms of human syndrome, providing a useful animal model to elucidate the pathophysiology of this problem in the LND.

Zizzo, M., Frinchi, M., Nuzzo, D., Jinnah, H., Mudò, G., Condorelli, D., et al. (2018). Altered gastrointestinal motility in an animal model of Lesch-Nyhan disease. AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL [10.1016/j.autneu.2017.12.007].

Altered gastrointestinal motility in an animal model of Lesch-Nyhan disease

Zizzo, Maria G.;Frinchi, Monica;Nuzzo, Domenico;Mudò, Giuseppa;CONDORELLI, DANIELE FILIPPO;Mulè, Flavia;Belluardo, Natale
;
Serio, Rosa
2018

Abstract

Mutations in the HGPRT1 gene, which encodes hypoxanthine-guanine phosphoribosyltransferase (HGprt), housekeeping enzyme responsible for recycling purines, lead to Lesch-Nyhan disease (LND). Clinical expression of LND indicates that HGprt deficiency has adverse effects on gastrointestinal motility. Therefore, we aimed to evaluate intestinal motility in HGprt knockout mice (HGprt). Spontaneous and neurally evoked mechanical activity was recorded in vitro as changes in isometric tension in circular muscle strips of distal colon. HGprt tissues showed a lower in amplitude spontaneous activity and atropine-sensitivity neural contraction compared to control mice. The responses to carbachol and to high KCl were reduced, demonstrating a widespread impairment of contractility. L-NAME was not able in the HGprt tissues to restore the large amplitude contractile activity typical of control. In HGprt colon, a reduced expression of dopaminergic D1 receptor was observed together with the loss of its tonic inhibitory activity present in control-mice. The analysis of inflammatory and oxidative stress in colonic tissue of HGprt mice revealed a significant increase of lipid peroxidation associated with over production of oxygen free radicals. In conclusion, HGprt deficiency in mice is associated with a decrease in colon contractility, not dependent upon reduction of acetylcholine release from the myenteric plexus or hyperactivity of inhibitory signalling. By contrast the increased levels of oxidative stress could partially explain the reduced colon motility in HGprt mice. Colonic dysmotility observed in HGprt mice may mimic the gastrointestinal dysfunctions symptoms of human syndrome, providing a useful animal model to elucidate the pathophysiology of this problem in the LND.
Settore BIO/09 - Fisiologia
www.elsevier.com/locate/jans
Zizzo, M., Frinchi, M., Nuzzo, D., Jinnah, H., Mudò, G., Condorelli, D., et al. (2018). Altered gastrointestinal motility in an animal model of Lesch-Nyhan disease. AUTONOMIC NEUROSCIENCE: BASIC & CLINICAL [10.1016/j.autneu.2017.12.007].
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10447/253503
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