| First Author | Clancy JS | Year | 1999 |
| Journal | Am J Physiol | Volume | 277 |
| Issue | 4 Pt 2 | Pages | R1205-9 |
| PubMed ID | 10516263 | Mgi Jnum | J:58138 |
| Mgi Id | MGI:1346767 | Doi | 10.1152/ajpregu.1999.277.4.r1205 |
| Citation | Clancy JS, et al. (1999) Contractile function is unaltered in diaphragm from mice lacking calcium release channel isoform 3. Am J Physiol 277(4 Pt 2):R1205-9 |
| abstractText | Skeletal muscle expresses at least two isoforms of the calcium release channel in the sarcoplasmic reticulum (RyR1 and RyR3). Whereas the function of RyR1 is well defined, the physiological significance of RyR3 is unclear. Some authors have suggested that RyR3 participates in excitation-contraction coupling and that RyR3 may specifically confer resistance to fatigue. To test this hypothesis, we measured contractile function of diaphragm strips from adult RyR3-deficient mice (exon 2-targeted mutation) and their heterozygous and wild-type littermates. In unfatigued diaphragm, there were no differences in isometric contractile properties (twitch characteristics, force-frequency relationships, maximal force) among the three groups. Our fatigue protocol (30 Hz, 0.25 duty cycle, 37 degrees C) depressed force to 25% of the initial force; however, lack of RyR3 did not accelerate the decline in force production. The force-frequency relationship was shifted to higher frequencies and was depressed in fatigued diaphragm; lack of RyR3 did not exaggerate these changes. We therefore provide evidence that RyR3 deficiency does not alter contractile function of adult muscle before, during, or after fatigue. |
