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1.
Neurobiol Dis ; 69: 93-107, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24878511

ABSTRACT

After incomplete spinal cord injury (SCI), patients and animals may exhibit some spontaneous functional recovery which can be partly attributed to remodeling of injured neural circuitry. This post-lesion plasticity implies spinal remodeling but increasing evidences suggest that supraspinal structures contribute also to the functional recovery. Here we tested the hypothesis that partial SCI may activate cell-signaling pathway(s) at the supraspinal level and that this molecular response may contribute to spontaneous recovery. With this aim, we used a rat model of partial cervical hemisection which injures the bulbospinal respiratory tract originating from the medulla oblongata of the brainstem but leads to a time-dependent spontaneous functional recovery of the paralyzed hemidiaphragm. We first demonstrate that after SCI the PI3K/Akt signaling pathway is activated in the medulla oblongata of the brainstem, resulting in an inactivation of its pro-apoptotic downstream target, forkhead transcription factor (FKHR/FOXO1A). Retrograde labeling of medullary premotoneurons including respiratory ones which project to phrenic motoneurons reveals an increased FKHR phosphorylation in their cell bodies together with an unchanged cell number. Medulla infusion of the PI3K inhibitor, LY294002, prevents the SCI-induced Akt and FKHR phosphorylations and activates one of its death-promoting downstream targets, Fas ligand. Quantitative EMG analyses of diaphragmatic contractility demonstrate that the inhibition of medulla PI3K/Akt signaling prevents spontaneous respiratory recovery normally observed after partial cervical SCI. Such inhibition does not however affect either baseline contractile frequency or the ventilatory reactivity under acute respiratory challenge. Together, these findings provide novel evidence of supraspinal cellular contribution to the spontaneous respiratory recovery after partial SCI.


Subject(s)
Forkhead Transcription Factors/metabolism , Medulla Oblongata/physiopathology , Nerve Tissue Proteins/metabolism , Oncogene Protein v-akt/metabolism , Recovery of Function/physiology , Respiration , Spinal Cord Injuries/physiopathology , Animals , Cervical Vertebrae , Diaphragm/physiopathology , Disease Models, Animal , Female , Functional Laterality , Medulla Oblongata/drug effects , Medulla Oblongata/pathology , Motor Neurons/pathology , Motor Neurons/physiology , Neuronal Plasticity/drug effects , Neuronal Plasticity/physiology , Oncogene Protein v-akt/antagonists & inhibitors , Phosphatidylinositol 3-Kinases/metabolism , Phosphoinositide-3 Kinase Inhibitors , Phrenic Nerve/pathology , Phrenic Nerve/physiopathology , Rats, Sprague-Dawley , Recovery of Function/drug effects , Respiration/drug effects , Signal Transduction/drug effects , Spinal Cord Injuries/pathology , Time Factors
2.
Exp Neurol ; 229(1): 120-31, 2011 May.
Article in English | MEDLINE | ID: mdl-20633558

ABSTRACT

Engraftment of nasal olfactory ensheathing cells (OEC) is considered as a promising therapeutic strategy for spinal cord repair and one clinical trial has already been initiated. However, while the vast majority of fundamental studies were focused on the recovery of locomotor function, the efficiency of this cellular tool for repairing respiratory motor dysfunction, which affects more than half of paraplegic/tetraplegic patients, remains unknown. Using a rat model that mimics the mechanisms encountered after a cervical contusion that induces a persistent hemi-diaphragmatic paralysis, we assessed the therapeutic efficiency of a delayed transplantation (2 weeks post-contusion) of nasal OECs within the injured spinal cord. Functional recovery was quantified with respiratory behavior tests, diaphragmatic electromyography and neuro-electrophysiological recording of the phrenic motoneurons while axogenesis was evaluated using immunohistochemistry. We show that 3 months post-transplantation, nasal OECs improve i) breathing movements, ii) activities of the ipsilateral diaphragm and corresponding phrenic nerve, and iii) axonal sprouting in the injury site. We also demonstrate that this functional partial recovery is mediated by the restoration of ipsilateral supraspinal command. Our study brings further evidence that olfactory ensheathing cells could have clinical application especially in tetraplegic patients with impaired breathing movements. This article is part of a Special Issue entitled: Understanding olfactory ensheathing glia and their prospect for nervous system repair.


Subject(s)
Cervical Vertebrae , Disease Models, Animal , Olfactory Bulb/transplantation , Recovery of Function/physiology , Respiratory Mechanics/physiology , Spinal Cord Injuries/surgery , Animals , Cell Transplantation/methods , Cell Transplantation/physiology , Female , Nasal Mucosa/physiology , Nasal Mucosa/transplantation , Olfactory Bulb/physiology , Rats , Rats, Sprague-Dawley , Spinal Cord Injuries/physiopathology , Spinal Cord Regeneration/physiology
3.
Int J Obes (Lond) ; 33(12): 1348-55, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19773740

ABSTRACT

OBJECTIVES: The involvement of skeletal muscle mitochondrial uncoupling protein-3 (UCP3) in the control of energy expenditure in skeletal muscle and at the whole-body level is still a matter of debate. We previously reported that UCP3 downregulation is linked to an enhanced mitochondrial energy metabolism in rat skeletal muscle as a result of acute capsiate treatment. Here, we aimed at investigating noninvasively the effects of chronic capsiate ingestion on metabolic changes occurring in exercising gastrocnemius muscle and at the whole-body level. METHODS: We used an original experimental setup allowing a complete noninvasive investigation of gastrocnemius muscle function in situ using 31-phosphorus magnetic resonance spectroscopy. Whole-body fat composition was determined using magnetic resonance imaging and UCP3 gene expression was measured by quantitative real-time RT-PCR analysis. RESULTS: We found that a 14-day daily administration of capsiate (100 mg kg(-1) body weight) reduced UCP3 gene expression and increased phosphocreatine level at baseline and during the stimulation period in gastrocnemius muscle. During muscle stimulation, pH(i) showed a larger alkalosis in the capsiate group suggesting a lower glycolysis and a compensatory higher aerobic contribution to ATP production. Although the capsiate-treated rats were hyperphagic as compared to control animals, they showed a lower weight gain coupled to a decreased abdominal fat content. CONCLUSION: Overall, our data indicated that capsiate administration contributes to the enhancement of aerobic ATP production and the reduction of body fat content coupled to a UCP3 gene downregulation.


Subject(s)
Abdominal Fat/drug effects , Capsaicin/analogs & derivatives , Energy Metabolism/drug effects , Ion Channels/metabolism , Mitochondrial Proteins/metabolism , Muscle, Skeletal/drug effects , Uncoupling Agents/pharmacology , Abdominal Fat/metabolism , Animals , Capsaicin/administration & dosage , Capsaicin/pharmacology , Down-Regulation , Energy Metabolism/physiology , Female , Mitochondria, Muscle/metabolism , Muscle, Skeletal/metabolism , Oxidation-Reduction/drug effects , Rats , Uncoupling Agents/administration & dosage , Uncoupling Protein 3
4.
Am J Physiol Endocrinol Metab ; 292(5): E1474-82, 2007 May.
Article in English | MEDLINE | ID: mdl-17264228

ABSTRACT

Although it has been suggested that the skeletal muscle mitochondrial uncoupling protein-3 (UCP3) is involved in regulating energy expenditure, its role is still poorly understood. In the present study, we aimed at investigating noninvasively, using magnetic resonance techniques, metabolic changes occurring in exercising muscle as a result of capsiate treatment, which has been previously linked to UCP3 upregulation. We showed that capsiate ingestion strongly reduced UCP3 gene expression in rat gastrocnemius muscle. This large underexpression was accompanied by a significant increase in the rate of mitochondrial ATP production and phosphocreatine level both at rest and during muscle stimulation. Similarly, the stimulation-induced ATP fall and ADP accumulation were significantly less after capsiate administration than in untreated rats. The larger oxidative ATP production rate could not be explained by a proportional decrease in the anaerobic component, i.e., glycolysis and phosphocreatine breakdown. In addition, the mechanical performance was not affected by capsiate administration. Finally, the plasma free fatty acid (FFA) level increased in capsiate-treated rats, whereas no significant change was observed after muscle stimulation in the control group. Considering the corresponding enhanced UCP3 mRNA expression occurring in the control group after muscle stimulation, one can suggest that changes in FFA level and UCP3 mRNA expression are not mechanistically correlated. Overall, we have shown that capsiate administration induced a UCP3 downregulation coupled with an increased mitochondrial ATP synthesis, whereas the muscle force-generating capacity was unchanged. This suggests that a decrease in muscle efficiency and/or additional noncontractile ATP-consuming mechanisms result from UCP3 downregulation.


Subject(s)
Analgesics, Non-Narcotic/pharmacology , Capsaicin/analogs & derivatives , Ion Channels/metabolism , Mitochondria, Muscle/metabolism , Mitochondrial Proteins/metabolism , Muscle, Skeletal/metabolism , Adenosine Diphosphate/metabolism , Adenosine Triphosphate/metabolism , Animals , Capsaicin/pharmacology , Down-Regulation/drug effects , Electric Stimulation , Energy Metabolism , Fatty Acids, Nonesterified/blood , Female , Hydrogen-Ion Concentration , Ion Channels/biosynthesis , Ion Channels/genetics , Magnetic Resonance Spectroscopy , Mitochondria, Muscle/drug effects , Mitochondrial Proteins/biosynthesis , Mitochondrial Proteins/genetics , Muscle, Skeletal/drug effects , Phosphocreatine/metabolism , Rats , Rats, Sprague-Dawley , Uncoupling Protein 3
5.
Cell Mol Biol (Noisy-le-grand) ; 46(7): 1249-58, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11075954

ABSTRACT

Alpine Marmots (Marmota marmota) are a good model to study intraspecific chemical communication among mammals. This species has been subjected to several behavioural and biochemical studies regarding both their scent-marking behaviour by cheek-rubbing, and the chemical composition of their glandular secretions. However, no molecular study has been undertaken until today on proteins from the olfactory epithelium possibly implicated in chemical perception. In this study, we identified, to our knowledge for the first time, some olfatory receptors from this wild rodent. Starting with olfactory epithelium of an Alpine Marmot, and by mean of reverse transcriptase polymerase chain reaction technique (RT-PCR), we isolated fourteen partial sequences that exhibited a high degree of homology (45-92%) with olfactory receptors from other vertebrates. Conserved identities and structural features clearly defined these Alpine Marmot sequences as members of the seven transmembrane domain olfactory receptors. All sequences were observed as belonging to known olfactory receptor families and were classified into ten subfamilies of the tetrapods OR class. Finally, Northern blot analysis revealed specific expression of these sequences in the Alpine Marmot olfactory epithelium tissue.


Subject(s)
Marmota/genetics , Receptors, Odorant/genetics , Amino Acid Sequence , Animals , Cloning, Molecular , Molecular Sequence Data , Olfactory Mucosa/metabolism , Phylogeny , RNA, Messenger/genetics , RNA, Messenger/metabolism , Receptors, Odorant/chemistry , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment
6.
Neurosci Lett ; 249(2-3): 87-90, 1998 Jun 19.
Article in English | MEDLINE | ID: mdl-9682823

ABSTRACT

Binding to olfactory receptors is the first step in odorant and pheromonal recognition and discrimination. These receptors constitute one of the most important, although poorly known, families of neuronal receptors. In this study we used degenerated oligonucleotides and a RT-PCR approach to selectively amplify olfactory receptors in the nasal epithelium of the domestic pig Sus scrofa. Several combinations of oligonucleotide were tested and allowed the isolation of eleven different partial sequences belonging to the seven transmembrane olfactory receptor family. These receptors formed a separate family within the seven transmembrane receptor superfamily in pigs. Using the criteria of Ben Arie et al. [Ben-Arie N., Lancet D., Taylor C., Khen M., Walker N., Ledbetter DH., Carrozzo R., Patel K., Sheer D., Lehrah H. and North M., Hum. Mol. Genet., 3 (1994) 229-235], the 11 receptors described here can be classified into three known families and seven subfamilies (one known and six new).


Subject(s)
Olfactory Mucosa/chemistry , Olfactory Receptor Neurons/chemistry , Swine/genetics , Amino Acid Sequence , Animals , Humans , Molecular Sequence Data , Oligonucleotides , Phylogeny , Polymerase Chain Reaction , Sequence Homology, Amino Acid
7.
G Ital Cardiol ; 17(6): 543-5, 1987 Jun.
Article in Italian | MEDLINE | ID: mdl-3666381

ABSTRACT

A case of vertebral fracture following DC shock for ventricular fibrillation is reported. After a short review of the complications of this procedure the case is described and compared with two other cases known in literature. We conclude that, although this complication is uncommon, it must be kept in mind owing to its potential severity.


Subject(s)
Electric Countershock/adverse effects , Fractures, Bone/etiology , Lumbar Vertebrae , Aged , Fractures, Bone/diagnostic imaging , Humans , Lumbar Vertebrae/diagnostic imaging , Male , Radiography , Ventricular Fibrillation/therapy
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