Creature Thinking
Adopting the acceptance from the local creature care panel, seven domestic pigs having a body weight (BW) away from 42–forty two kilogram have been tested. New pet was in fact operatively instrumented in a manner that synchronous catheter-founded IPM had been you can easily in the MPA and also in the new iliac artery (IA). That have catheters inside situ and you can intubated yet not vented, the dogs were put-on the newest table of your MR scanner on supine reputation. In most pets, normocapnia are tracked from the frequent arterial blood gasoline research from inside the whole sedation.
Pulmonary Hypertension (PAH)
Several experimental designs with various invasiveness have been published to evaluate PAH: open chest models with constriction of the MPA ( 19 ), implanted balloon catheters in the left atrium ( 20 ), injection of microspheres ( 21 ), surgical creation of arteriovenous (av)-fistulas ( 22 ), variations in circulating blood volume inducing an elevation of the pulmonary pressure ( 23 ), and injections of serotonin ( 24 , 25 ). In this study, PAH was generated experimentally by continuous intravenous application of thromboxane A2 (TxA2, C20H32O5), a prostaglandin with a half-life in the range of seconds. TxA2 is known to induce a transient, but intense, constriction of the pulmonary arteries with negligible constrictive effects on the systemic circulation. To examine different degrees of severity of PAH, TxA2 was applied at dosages of 0.075, 0.1, and 0.125 ?g/kg BW/minute. In each pig, five IPM and five MR velocity-encoded measurements were obtained at different pulmonary pressure levels. First, basic values without TxA2 were acquired. Second, three different stages of PAH induced by TxA2 were measured. Third, after devolution of TxA2 and recovery of stable pressure levels in the MPA as measured with IPM, a final measurement was performed. Accordingly, seven ? five synchronously acquired MR velocity encoded and IPM data sets were generated.
The brand new catheter-based study buy is completed with Berman angiographic catheters (Arrow Globally Inc., Reading, PA, USA) getting IPM associated with an effective MR-compatible monitoring device (OmniTrak 7000, Inside the Vivo Research, Inc., Orlando, Fl, USA). Zero positioning is over before specifications. IPM try recorded consistently and you may integrated the purchase of one’s systolic plus the suggest pressure from the MPA and in the newest IA paralleling the 5 MR proportions.
MR Acceleration-Encoded Measurements
The MR flow measurement technique has been validated and utilized before in a pediatric study on normal values in the pulmonary circulation ( 26 ). Velocity-encoded MR measurements were performed in a 1.5 Tesla system (Magnetom Sonata, Siemens Medical Solutions, Erlangen, Germany) using a phase-contrast fast low angle shot (FLASH)-sequence. Former publications using Doppler ultrasonography to quantify pulmonary hypertension ( 17 ) pointed to the importance of an accurate registration of the AT. Therefore, a high temporal resolution should also be achieved with the MR velocity-encoded measurements. Maximum gradient settings (gradient strength = 40 mT/m, slew rate = 200 T/m/second, rise time = 200 ?s) combined with a bandwidth of 1395 Hertz/pixel resulted in a minimum TE and TR of 2.4 msec and 9.5 msec, respectively. With the selected sequence, TR equaled the temporal resolution. The MPA was centered in the B0 field as far as possible to minimize phase shift errors due to eddy currents ( 27 ) and Maxwell term correction was applied. Three measurements were averaged to increase the signal-to-noise ratio, requiring a heart frequency–dependent acquisition time of approximately seven to 10 minutes. Measurements were performed during free breathing to include the effects of respiration on cardiac output and pulmonary flow ( 18 ). The application of long-term averaging compensated for respiratory motion. The spatial resolution using a matrix size of 256 was 1.1 mm ? 1.4 mm, and the slice thickness was 5 mm. Using multiple scout images, the MR velocity-encoded imaging plane was measured perpendicularly to the MPA (Fig. 1). IPM and MR velocity-encoded geek2geek giriÅŸ measurements were simultaneously acquired before, during, and after experimentally induced pulmonary hypertension. MR flow measurement sequences allow to generate: 1) phase images (containing the direction-encoded quantitative velocity information); 2) magnitude images (containing the not quantitative information about the localization of any flow); and 3) rephased, i.e., anatomical images (with a similar appearance as T1-weighted gradient echo images). MR data sets were analyzed using commercially available flow quantification software (ARGUS®; Siemens Medical Solutions, Erlangen, Germany) to derive the morphological and flow related parameters from the MPA listed in Table 1.