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| Content Provider | Springer Nature Link |
|---|---|
| Author | Bassi, Mirian Giusti, Humberto Leite, Cristiane Mota Anselmo Franci, Janete A. Carmo, Jussara M. Silva, Alexandre A. Hall, John E. Colombari, Eduardo Glass, Mogens L. |
| Copyright Year | 2012 |
| Abstract | Previous studies showed that leptin-deficient (ob/ob) mice develop obesity and impaired ventilatory responses to CO2 $$ \left( {{{\dot{V}}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}}} \right) $$ . In this study, we examined if leptin replacement improves chemorespiratory responses to hypercapnia (7 % CO2) in ob/ob mice and if these effects were due to changes in body weight or to the direct effects of leptin in the central nervous system (CNS). $$ {\dot{V}_{{{\text{E}}\,}}}{\text{ - C}}{{\text{O}}_{{2}}} $$ was measured via plethysmography in obese leptin-deficient- (ob/ob) and wild-type- (WT) mice before and after leptin (10 μg/2 μl day) or vehicle (phosphate buffer solution) were microinjected into the fourth ventricle for four consecutive days. Although baseline $$ {\dot{V}_{\text{E}}} $$ was similar between groups, obese ob/ob mice exhibited attenuated $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ compared to WT mice (134 ± 9 versus 196 ± 10 ml min−1). Fourth ventricle leptin treatment in obese ob/ob mice significantly improved $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ (from 131 ± 15 to 197 ± 10 ml min−1) by increasing tidal volume (from 0.38 ± 0.03 to 0.55 ± 0.02 ml, vehicle and leptin, respectively). Subcutaneous leptin administration at the same dose administered centrally did not change $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ in ob/ob mice. Central leptin treatment in WT had no effect on $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ . Since the fourth ventricle leptin treatment decreased body weight in ob/ob mice, we also examined $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ in lean pair-weighted ob/ob mice and found it to be impaired compared to WT mice. Thus, leptin deficiency, rather than obesity, is the main cause of impaired $$ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $$ in ob/ob mice and leptin appears to play an important role in regulating chemorespiratory response by its direct actions on the CNS. |
| Starting Page | 145 |
| Ending Page | 153 |
| Page Count | 9 |
| File Format | |
| ISSN | 00316768 |
| Journal | Pflügers Archiv |
| Volume Number | 464 |
| Issue Number | 2 |
| e-ISSN | 14322013 |
| Language | English |
| Publisher | Springer-Verlag |
| Publisher Date | 2012-05-15 |
| Publisher Place | Berlin, Heidelberg |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Respiratory chemoreception Obesity Hypercapnia Leptin Ventilation Human Physiology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physiology Physiology (medical) Clinical Biochemistry |
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