Giovannelli L, Giovannini M G, Pedata F, Pepeu G
Department of Preclinical and Clinical Pharmacology, University of Florence, Italy.
Exp Gerontol. 1988;23(3):175-81. doi: 10.1016/0531-5565(88)90004-6.
The effect of adenosine, N-ethylcarboxamide adenosine (NECA), and caffeine on acetylcholine (ACh) release was investigated in cortical slices prepared from 3 and 22-24-month-old rats. The slices were perfused with Krebs solution and electrically stimulated at 0.2, 1, and 5 Hz stimulation frequency. In old rats, ACh released by stimulation at 1 and 5 Hz was about half as large as in adult rats. In 22-24-month-old rats, the potency of adenosine was strongly reduced, and a similar significant inhibition of ACh release was obtained with concentrations of 1 microM adenosine in adult and 300 microM in old rats. Conversely, NECA, which has no effect on ACh release in adult rats, brought about a 40% decrease in old rats. Caffeine at 50 microM concentration enhanced, and at 500 microM inhibited, the evoked ACh release in adult rats, but was inactive in old rats. The possibility is envisaged that aging may modify purinergic modulation of ACh release by inducing conformational changes in purinergic receptors or changing adenosine metabolism.
研究了腺苷、N-乙基甲酰胺腺苷(NECA)和咖啡因对3月龄及22 - 24月龄大鼠制备的皮质切片中乙酰胆碱(ACh)释放的影响。切片用 Krebs 溶液灌注,并以0.2、1和5Hz的刺激频率进行电刺激。在老年大鼠中,1Hz和5Hz刺激释放的ACh约为成年大鼠的一半。在22 - 24月龄大鼠中,腺苷的效力大幅降低,成年大鼠中1μM腺苷和老年大鼠中300μM腺苷对ACh释放产生了类似的显著抑制。相反,NECA对成年大鼠的ACh释放没有影响,但在老年大鼠中导致ACh释放减少40%。50μM浓度的咖啡因增强了成年大鼠诱发的ACh释放,而500μM则抑制了该释放,但在老年大鼠中无活性。设想衰老可能通过诱导嘌呤能受体的构象变化或改变腺苷代谢来改变对ACh释放的嘌呤能调节。