The phrase "administration vehicles" is correct and usable in written English.
It can be used to refer to vehicles that are specifically designated for administrative purposes, such as transporting staff or conducting official business.
Example: "The company has recently acquired new administration vehicles to improve efficiency in transporting employees to various locations."
Alternatives: "official vehicles" or "administrative transport".
Because each mouse had two chances of administration (vehicle vs. overwaking drug, or vehicle vs. oversleeping drug), total length of 2 days were used for the test per animal.
Then, the animals were divided into the following groups: vehicle-treated rats without alcohol administration (vehicle group); Ad-GFP-treated rats without alcohol administration (Ad-GFP group); Ad-GFP-treated rats with alcohol administration (Alcohol + Ad-GFP group) and Ad-miR-382-treated rats with alcohol administration (Alcohol + Ad-miR-382 group).
Ghrelin and vehicle were injected IP after central administration of vehicle or NPY receptor antagonist.
There was no apparent change in viscoelasticity in the vehicle control cohort after 24 h of administration with vehicle (coefficient of variation of | G*|=13%).
10-week-old male C57BL/6NCrl mice (Charles Rivers Laboratories, Wilmington, MA) were randomly assigned to four groups: 1) sham followed by administration of vehicle only; 2) sham followed by UDCA administration; 3) BDL followed by administration of vehicle only and 4) BDL followed by UDCA administration.
Wild-type mice were injected with vehicle (10% Tween 80 IP) or VU0467154 (30 mg/kg, IP), followed 30 min later by administration of vehicle (saline IP) or MK-801 (0.3 mg/kg, IP).
Mice were administered vehicle or 5-hydroxydecanoate (5-HD) intravenously 10 min before LAD occlusion followed by a single intravenous administration of vehicle or DDFPe immediately after occlusion.
bolus injections of ergotamine were determined after administration of vehicle or several α1⧸2-adrenoceptor antagonists.
Hourly plots of NREM (A) and REM (B) sleep after oral administration of vehicle (open circles) or octacosanol (blue circles).
(A) Typical examples of EEG delta power (0.5 4 Hz), EMG integral, and hypnograms of a mouse after p.o. administration of vehicle or octacosanol.
In contrast, prior administration of vehicle instead of caffeine did not disrupt the acupuncture analgesia (−49.4 ± 3.9% change, p < 0.001 compared to Before acupuncture) (Fig. 3B,C).
