Goel, V.K.; Joshi, B.C.
Effect of metabolic inhibitors, namely, actinomycin-D and mitomycin-C on 3 H-lysine incorporation in the stilbestrol stimulated chick oviduct has been studied. It was inferred from the study that the action of the metabolic inhibitors used may be dependent on the level of the hormone present or in other words, on the rate at which the protein synthesis is going on in the system. Mitomycin-C has the same effect in this system as actinomycin-D but at a dose level almost 4 times that of the latter. The results are discussed in the light of the findings of other workers. (author)
Tumor affinity of technetium-99m labeled radiopharmaceuticals. II. Sup(99m)Tc-Sn-diphosphonate (sup(99m)Tc-EHDP), sup(99m)Tc-Sn-dimercaptosuccinic acid (sup(99m)Tc-DMSA), sup(99m)Tc-Sn-diethyl stilbestrol diphosphate (sup(99m)Tc-DSDP)
Itoh, K; Kobayashi, S; Hisada, K; Tonami, N [Kanazawa Univ. (Japan). School of Medicine; Ando, A
The authors have examined the tumor affinity of various sup(99m)Tc-labelled radiopharmaceuticals to Ehrlich's tumor for the purpose of delineating human malignant neoplasm positively. The biologic distributions of sup(99m)Tc-Sn-diphosphonate (sup(99m)Tc-EHDP), sup(99m)Tc-Sn-dimercaptosuccinic acid (sup(99m)Tc-DMSA) and sup(99m)Tc-Sn-diethyl stilbestrol diphosphate (sup(99m)Tc-DSDP, sup(99m)Tc-Honvan) are included as the second report on the tumor affinity of Ehrlich-bearing mice. Tumor concentration of sup(99m)Tc-EHDP was lowest and the positive delineation of implanted tumor with sup(99m)Tc-EHDP was poorest in sequential images, though active accumulation in some soft tissues malignant neoplasms, breast cancer, and thyroid cancer, has been reported. Tumor concentration and the tumor-to-blood ratio of sup(99m)Tc-DMSA were not so high, contrary to our expectation that /sup 197/Hg-DMSA might show high tumor concentration and high tumor-to-blood ratio the same as /sup 197/Hg chlormerodrin of the renal scanning radiopharmaceuticals. Tumor concentration of sup(99m)Tc-DSDP was highest. The tumor-to-blood concentration ratio was lower than that of the above mentioned radiopharmaceuticals but the tumor-to-liver ratio and/or tumor-to-lung ratio was over 1.0 at the earlier time. Biologic distribution of sup(99m)Tc-DSDP was similar to that of /sup 32/P labeled DSDP. It is presumed that sup(99m)Tc is labeled at the phosphate ester of DSDP which is dephospholytated immediately by phospholylase in vivo following intravenous injection. Although it is not known precisely it may be assumed that the mechanism of accumulating sup(99m)Tc-DSDP in Ehrlich's tumor is related to the phospholylase activity in neoplasms.
Tewari, P V; Chaturvedi, C; Dixit, S N
This study was undertaken to determine possible antifertility properties of the stalk of the betel plant, Piper betle, which is extensively cultivated in warm moist parts of India for its leaves. The thin stalks were dried, powdered, and extracted with alcohol; the residue was used in the study and named betel leaf stalk extract (BLSE). It was macerated with gum acacia, suspended in distilled water, and diluted to 25 mg/ml. The drug was fed by oral intubation. Initially 20 rats were used in 2 groups, one receiving BLSE 50 mg/kg body weight for 10 days and the other vehicle only. Both were caged with males for 15 days. Only 2 of 10 rats receiving BLSE gave birth to litters while 9 of 10 controls delivered. Number of pups was also reduced. In another experiment using 60 female rats to 30 while BLSE at 50 mg/100 gm body weight was fed for 3 days during diestrus to 30 while 30 controls received vehicle only. Successful mating was confirmed by sperm in vaginal smears. 8 of 30 treated rats delivered 3.5 pups each while 29 of 30 controls delivered 7 pups per rat. In a third experiment 10 female rats were given BLSE 50mg/100 gm body weight, 10 vehicle only, and 10 neoclinesterol 150 mcg/100 gm body weight for 4 consecutive days. On Day 5 the animals were sacrificed and weights of uterus and ovaries recorded. Antiestrogenic properties were studied in oophorectomized rats given stilbestrol 150 mcg/100 gm body weight by injection, then fed 150 mcg/100 gm body weight of neoclinesterol or BLSE, 50 mg/100 gm, but the neoclinesterol. Vaginal smears were examined for cornification on Days 2, 3, and 4. Progestational activity was studied in 12 immature female rabbits injected with stilbestrol then treated with BLSE or leutocycline. Tests for estrogenic and antiestrogenic activity of BLSE were negative. A mild progestational activity was found in immature estrogen-primed rabbits but some follicle depressant type action was noted as several graffian follicles were seen in their
Dong Lin; Zhu Chuanrong; Fu Wen; Xue Gaiqing; Xin Yu; Zhang Weijie; Sun Lijing; Chen Aiqun
Objective: To investigate the action of suppressing lactation with Vit B 6 after induced abortion in second trimester of pregnancy and its clinical application. Methods: 60 Subjects in the second trimester of pregnancy were induced abortion with intra-amniotic injection of 100 mg rivanol. 30 subjects were not given any drug after the procedure (serving as controls) and the another 30 subjects started Vit B 6 2h after operation. With a dose of 60 mg tid x 5 days P.o. Serum levels of PRL, E 2 , P Were determines with RIA before and on the 4 th day post-abortion. Presence or absence of lactation after abortion was observed by squeezing the breast in all subjects. Results: In both groups the post-operative serum levels of the three tested hormones were significantly lower than those before operation. The decrease of PRL was especially marked in the Vit B 6 group (P 6 group (6.66%, 2/30); while it was present in 9 controls (30%, 9/30). Conclusion: Starting Vit B 6 treatment with in 2h after terminal of pregnancy would very effectively suppress milk secretion (93.3%) and could satisfactorily replace the conventional stilbestrol treatment. Marked decrease in serum PRL level (42.85%) reflected a solid laboratory evidence