166the tonus of isolated guinea-pig lung parenchymal strip.Among the smooth muscle preparations tested, the most sensitive to PLS was found to be isolated, helically cut strips of rabbit arteries. Based on the present findings the biological activity of PLS differs from that of PGE 2 or PGE 1 which eliminates the possibility that PLS could be one of the E-prostaglandins or a mixture of them, which confirms our previous findings. The observed spectrum of activity of PLS resembles that of PGI2X~ both relax bovine coronary artery and rabbit mesenteric and coeliac arteries; both contract the rat stomach strip and both typically inhibit spontaneous movements of the isolated guinea-pig ileum. Therefore, to check the possibility that PLS could be identical with PGI2, their effects on platelet aggregation induced either by ADP or collagen have been determined. PLS, similarly to PGI2, inhibits platelet aggregation regardless of the inducer used. However, a few distinctions between the anti-aggregatory activity of PLS and that of PGI2 have been noted. One is that the anti-aggregatory activity of PLS is heat resistant, i.e., it is not destroyed by immersion in a 100 ~ water bath for 15 sec. Secondly, the anti-aggregatory activity of PLS is preferentially directed against collagen. When 10 gM of ADP is used to induce platelet aggregation, the 1C50 for PLS is between 70-80 gl/ ml; and when 5 gg of collagen per ml of PRP is used to induce platelet aggregation the 1C50 for PLS is between 0.5-2.0 gl/ml. It therefore seems that the anti-aggregatory activity of PLS against collagen is about 70 times higher than that against ADP. Third, there is a quantitative difference between the de-aggregatory activities of PLS and PGI 2 (de-aggregation is defined as the light transmittance decrease, correlated to the amount of PGI 2 added at the Experientia 37 (1981), Birkh~iuser Verlag, Basel (Schweiz) height Of collagen-induced aggregation). In that respect PLS is about 10 times weaker than PGI 2. The prostaglandins and related compounds constitute a complex system both regarding their effects as smooth muscle stimulants and their ability to enhance or else inhibit platelet aggregation. This study indicates that PLS is not identical with primary prostaglandins or PGI 2. The present data confirm the powerful and specific biological activity of these compounds. Moreover, PLS possess a unique pattern in their anti-aggregatory effect on platelets. It seems that PLS constitute a new type of bacterial metabolite. However, how these substances contribute on the inflammatory sequelae of acne vulgaris remains to be determined. Summary. Both in acute and chronic cats entopeduncular stimulation inhibits, to a greater extent than caudate activation, focal paroxysmal activity in the ventro-basal complex of the amygdala. Lesion of entopeduncular neurons, by means of kainic acid injection, induces a decrease of the caudate inhibitory effect. It is suggested that neostriatal control of the amygdaloid seizures occurs partly through the globus pallidus.It has...