{"Procedure":"<p>3.1 Calculate and record the volume of anaesthetic solution required for intraperitoneal (IP) injection.</p><p>3.2 Anesthetize the mice.</p><p>3.3 Monitor the animal carefully until unconsciousness by ensuring that the mouse is adequately sedated.</p><p>3.4 Weigh the mouse and record the value.</p><p>3.5 Measure the length of the mouse as follows and record the value (accuracy ±0.1cm)</p><p>3.5.1 Place the unconscious mouse on a disinfected ruler so that its nose is at zero</p><p>(figure 1).</p><p><img src=\"https://api.mousephenotype.org/impress/image/a829fd141ffa7626fbf640550df0cfd8bef837d893d25885b1eeb2b5ea2ae7e1\"></p><p>Figure 1</p><p>3.5.2 To measure the entire length of the head press gently against the ruler</p><p>(figure 2) and gently pull the tail to ensure that the spine returns to its full</p><p>length (figure 3).</p><p><img src=\"https://api.mousephenotype.org/impress/image/b1f12d54fff821d05284ba7f379d81472b384831ad4973897d973d6facdefbc7\"></p><p>Figure 2</p><p><img src=\"https://api.mousephenotype.org/impress/image/2666263a24f43572af79a61384b35b48fb5488f1251e84e16ee0f819f24da9d2\"></p><p>Figure 3</p><p>3.5.3 Measure the length starting from the nose (0cm) to the beginning of the tail</p><p>(figure 4). Record the measurement &ndash; the accuracy is within 0.1cm. For</p><p>example in figure 4 the length of the mouse is 9.5cm.</p><p><img src=\"https://api.mousephenotype.org/impress/image/79e5372f68c9124e05c245f7e3f047423cd2b868b75e3dee0eb26ee3a54584fb\"></p><p>Figure 4</p><p>3.5.4 Disinfect the ruler and contact area after the measurement has been taken.</p><p>3.6 Place the unconscious mouse into the DEXA analyser.</p><p>3.7 Perform a scout-scan.</p><p>3.8 Optimise the area of interest and perform a measure-scan.</p><p>3.9 Note that the exposure dose per mouse is 300μSv.</p><p>3.10 For the analysis of the data, regions of interest must be defined. The standard analysis comprises of a whole body analysis excluding the head area.</p><p>Continue with X-ray analysis or</p><p>3.11 Remove the mouse once the image is captured. Place the mouse on a heated mat, set at 37ºC, in a cage and monitor closely until consciousness is regained.</p>","Purpose":"<p>\r\n\tMeasure bone mineral content and density as well as body composition in mice using the DEXA (Dual Energy X-ray Absorptiometry) analyser.</p>\r\n","Experimental Design":"<ul>\n\t<li>\n\t\t<strong>Age at test:</strong> Females at 16 and 51 weeks.</li>\n</ul>\n","Notes":"<p>\n\tDual-energy X-ray Absorptiometry (DEXA or DXA) is a method of quantifying bone mineral content and density. DXA uses an X-ray generator of high stability to produce photons over a broad spectrum of energy levels. Its photon output is filtered to produce the two distinct peaks necessary to distinguish bone from soft tissue.</p>\n<p>\n\tThe technique used for separating photon output into two distinct energy levels is known as &lsquo;K-edge&rsquo; filtration. By placing a filter element in the beam path, energy levels reacting with the filter material are sharply attenuated. The filter effect gradually lessens at higher energy levels, and so a second peak is introduced. The tin filter material used in this system produces energy peaks at 28keV and 48keV. Two solid-state detectors and proprietary energy discrimination are used to determine high and low energy counts.</p>\n<p>\n\tThe count data is transformed by software into bone and non-bone components, thus generating the bone density values. Information is generated about body weight, body length, fat and bone mass, bone mass density, and lean mass of each mouse.</p>\n<p>\n\t<strong>Data QC</strong></p>\n<p>\n\tCalibration of the system is done in daily intervals using the phantoms delivered by the manufacturer. The results from the calibration runs are recorded by the system.</p>\n"}