Chang M C, Berkery D, Schuel R, Laychock S G, Zimmerman A M, Zimmerman S, Schuel H
Department of Anatomical Sciences, School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York 14214.
Mol Reprod Dev. 1993 Dec;36(4):507-16. doi: 10.1002/mrd.1080360416.
Delta-9-tetrahydrocannabinol ((-)delta 9 THC), the primary psychoactive cannabinoid in marihuana, reduces the fertilizing capacity of sea urchin sperm by blocking the acrosome reaction that normally is stimulated by a specific ligand in the egg's jelly coat. The bicyclic synthetic cannabinoid [3H]CP-55,940 has been used as a ligand to demonstrate the presence of a cannabinoid receptor in mammalian brain. We now report that [3H]CP-55,940 binds to live sea urchin (Strongylocentrotus purpuratus) sperm in a concentration, sperm density, and time-dependent manner. Specific binding of [3H]CP-55,940 to sperm, defined as total binding displaced by (-)delta 9THC, was saturable: KD 5.16 +/- 1.02 nM; Hill coefficient 0.98 +/- 0.004. This suggests a single class of receptor sites and the absence of significant cooperative interactions. Sea urchin sperm contain 712 +/- 122 cannabinoid receptors per cell. Binding of [3H]CP-55,940 to sperm was reduced in a dose-dependent manner by increasing concentrations of CP-55,940, (-)delta 9THC, and (+)delta 9THC. The rank order of potency to inhibit binding of [3H]CP-55,940 to sperm and to block the egg jelly stimulated acrosome reaction was: CP-55,940 > (-)delta 9THC > (+)delta 9THC. These findings show that sea urchin sperm contain a stereospecific cannabinoid receptor that may play a role in inhibition of the acrosome reaction. The radioligand binding data obtained with live sea urchin sperm are remarkably similar to those previously published by other investigators using [3H]CP-55,940 on mammalian brain and nonneural tissues. The cannabinoid binding properties of this receptor appear to have been highly conserved during evolution. We postulate that the cannabinoid receptor may modulate cellular responses to stimulation.
Δ⁹-四氢大麻酚((-)Δ⁹ THC)是大麻中的主要精神活性大麻素,它通过阻断顶体反应来降低海胆精子的受精能力,而顶体反应通常是由卵胶膜中的特定配体刺激引发的。双环合成大麻素[³H]CP - 55,940已被用作配体来证明哺乳动物大脑中存在大麻素受体。我们现在报告,[³H]CP - 55,940以浓度、精子密度和时间依赖性方式与活海胆(紫海胆)精子结合。[³H]CP - 55,940与精子的特异性结合(定义为被(-)Δ⁹ THC取代的总结合)是可饱和的:解离常数(KD)为5.16 ± 1.02 nM;希尔系数为0.98 ± 0.004。这表明存在单一类别的受体位点且不存在显著的协同相互作用。海胆精子每个细胞含有712 ± 122个大麻素受体。随着CP - 55,940、(-)Δ⁹ THC和(+)Δ⁹ THC浓度的增加,[³H]CP - 55,940与精子的结合呈剂量依赖性降低。抑制[³H]CP - 55,940与精子结合以及阻断卵胶膜刺激的顶体反应的效力顺序为:CP - 55,940 > (-)Δ⁹ THC > (+)Δ⁹ THC。这些发现表明海胆精子含有立体特异性大麻素受体,该受体可能在抑制顶体反应中发挥作用。用活海胆精子获得的放射性配体结合数据与其他研究人员先前在哺乳动物大脑和非神经组织上使用[³H]CP - 55,940发表的数据非常相似。该受体的大麻素结合特性在进化过程中似乎高度保守。我们推测大麻素受体可能调节细胞对刺激的反应。