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Following a 1 week recovery period, each mouse received an injection once every 4 or 5 days a half hour prior to recording.
Immediately after LAD-ligation, each mouse received an intramyocardial injection of 400.000 hMSC in BD Matrigel™ Matrix BD Biosciences USAA), or BD Matrigel™ Matrix alone for MI-C similar to a previous study [59].
On day 7 the 21 days stress phase begun and each resident mouse received an unfamiliar same-sex weight-matched intruder mouse and the two animals were allowed to freely interact for 10 minutes.
Each mouse received an intravenous injection of LT (100 µg/g, LF PA = 1∶5), a lethal dose for mice, with or without pretreatment of photocatalysis on TiO2 (N) or TiO2 substrates (3×104 lux, 10 minutes at 4°C or 25°C).
Before sacrifice, each mouse received an osmotic minipump containing [3H] thymidine.
Each mouse received an accurate 0.1 mL of the emulsion each time.
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Each mouse received a total of ∼3×107 cfu.
Each mouse received a subcutaneous (s.c).
A 'donor mouse' received a subcutaneous tumour cell implantation.
Each mouse received a single intraperitoneal (IP) injection of drug as indicated.
Each mouse received a preoperative subcutaneous injection of 1.5 mg oxytretracycline and 0.003 mg of buprenorphine.
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