Studies on the distribution of antitumor amino acid related compounds by whole body autoradiography in mice
Four novel antitumor amino acid related compounds were labeled with 14C and the distribution was studied in mice. *A-91 was excreted into the bile, and a high level of radioactivity in the blood was maintained throughout the 24 hr of experiment. A high radio-activity was seen in the liver, lung, kid...
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Veröffentlicht in: | Folia Pharmacologica Japonica 1974, Vol.70(6), pp.849-861 |
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description | Four novel antitumor amino acid related compounds were labeled with 14C and the distribution was studied in mice. *A-91 was excreted into the bile, and a high level of radioactivity in the blood was maintained throughout the 24 hr of experiment. A high radio-activity was seen in the liver, lung, kidney, urinary bladder, and tumor. *A-145 was rapidly distributed to each tissue from the blood, especially to the pancreas, salivary glands, gastrointestinal tract, tumor, and other growing and secreting tissue. *A-192 was excreted into the bile and a high level of radioactivity was seen in the blood. A high radioactivity was detected in the liver, lung, kidney, uterus, ovary, and tumor, followed by a reduction paralleled with a concentration in the blood. *A-192 was rapidly excreted into the urine and very little radioactivity was observed in almost all organs and tissues, except for the central nervous system. *Cyclophosphamide was also rapidly excreted into the urine and bile, but only slight activity was observed in most organs. *Tryptophan, *isoleucine, *valinethese three had the same distribution patterns, and were incorporated into the growing and secreting tissues, pancreas, salivary glands, gastrointestinal tract, tumor, etc. |
doi_str_mv | 10.1254/fpj.70.849 |
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School of Medicine</creatorcontrib><description>Four novel antitumor amino acid related compounds were labeled with 14C and the distribution was studied in mice. *A-91 was excreted into the bile, and a high level of radioactivity in the blood was maintained throughout the 24 hr of experiment. A high radio-activity was seen in the liver, lung, kidney, urinary bladder, and tumor. *A-145 was rapidly distributed to each tissue from the blood, especially to the pancreas, salivary glands, gastrointestinal tract, tumor, and other growing and secreting tissue. *A-192 was excreted into the bile and a high level of radioactivity was seen in the blood. A high radioactivity was detected in the liver, lung, kidney, uterus, ovary, and tumor, followed by a reduction paralleled with a concentration in the blood. *A-192 was rapidly excreted into the urine and very little radioactivity was observed in almost all organs and tissues, except for the central nervous system. *Cyclophosphamide was also rapidly excreted into the urine and bile, but only slight activity was observed in most organs. *Tryptophan, *isoleucine, *valinethese three had the same distribution patterns, and were incorporated into the growing and secreting tissues, pancreas, salivary glands, gastrointestinal tract, tumor, etc.</description><identifier>ISSN: 0015-5691</identifier><identifier>EISSN: 1347-8397</identifier><identifier>DOI: 10.1254/fpj.70.849</identifier><language>eng ; jpn</language><publisher>Japan: The Japanese Pharmacological Society</publisher><subject>AMINO ACIDS- TISSUE DISTRIBUTION ; ANTINEOPLASTIC DRUGS- TISSUE DISTRIBUTION ; AUTORADIOGRAPHY- CARBON 14 COMPOUNDS ; BILE ; BLOOD ; KIDNEYS ; LIVER ; LUNGS ; METABOLISM ; MICE ; N48830 -Life Sciences-New Tracer Techniques-Other ; TIME DEPENDENCE ; UPTAKE</subject><ispartof>Folia Pharmacologica Japonica, 1974, Vol.70(6), pp.849-861</ispartof><rights>The Japanese PharmacologicalSociety</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,881,4010,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/4215593$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>NAGANUMA, Mariko</creatorcontrib><creatorcontrib>FUKUSHIMA, Koji</creatorcontrib><creatorcontrib>TOYOSHIMA, Shigeshi</creatorcontrib><creatorcontrib>Keio Univ., Tokyo (Japan). School of Medicine</creatorcontrib><title>Studies on the distribution of antitumor amino acid related compounds by whole body autoradiography in mice</title><title>Folia Pharmacologica Japonica</title><description>Four novel antitumor amino acid related compounds were labeled with 14C and the distribution was studied in mice. *A-91 was excreted into the bile, and a high level of radioactivity in the blood was maintained throughout the 24 hr of experiment. A high radio-activity was seen in the liver, lung, kidney, urinary bladder, and tumor. *A-145 was rapidly distributed to each tissue from the blood, especially to the pancreas, salivary glands, gastrointestinal tract, tumor, and other growing and secreting tissue. *A-192 was excreted into the bile and a high level of radioactivity was seen in the blood. A high radioactivity was detected in the liver, lung, kidney, uterus, ovary, and tumor, followed by a reduction paralleled with a concentration in the blood. *A-192 was rapidly excreted into the urine and very little radioactivity was observed in almost all organs and tissues, except for the central nervous system. *Cyclophosphamide was also rapidly excreted into the urine and bile, but only slight activity was observed in most organs. *Tryptophan, *isoleucine, *valinethese three had the same distribution patterns, and were incorporated into the growing and secreting tissues, pancreas, salivary glands, gastrointestinal tract, tumor, etc.</description><subject>AMINO ACIDS- TISSUE DISTRIBUTION</subject><subject>ANTINEOPLASTIC DRUGS- TISSUE DISTRIBUTION</subject><subject>AUTORADIOGRAPHY- CARBON 14 COMPOUNDS</subject><subject>BILE</subject><subject>BLOOD</subject><subject>KIDNEYS</subject><subject>LIVER</subject><subject>LUNGS</subject><subject>METABOLISM</subject><subject>MICE</subject><subject>N48830 -Life Sciences-New Tracer Techniques-Other</subject><subject>TIME DEPENDENCE</subject><subject>UPTAKE</subject><issn>0015-5691</issn><issn>1347-8397</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1974</creationdate><recordtype>article</recordtype><recordid>eNo90E1LxDAQBuAgCi66F39B8Ch0TdKkH0dZ_IIFD-o5pMlkm7VtliRF-u_tUtlLBjLPDMOL0B0lG8oEf7THw6Ykm4rXF2hFc15mVV6Xl2hFCBWZKGp6jdYxuoYQUbKyyOkK_Xym0TiI2A84tYCNiym4Zkxu_vAWqyG5NPY-YNW7wWOlncEBOpXAYO37ox8HE3Ez4d_Wd4AbbyasxuSDMs7vgzq2E3YD7p2GW3RlVRdh_V9v0PfL89f2Ldt9vL5vn3aZZvPBmSHCioZWRnBLjTYVqFpXlLCKWa5JxQ1jPC8KS1lVq9LWmoh8hlwAgBU0v0H3y14fk5NRuwS61X4YQCfJGRWizmf0sCAdfIwBrDwG16swSUrkKU45xylLIuc4Z7xd8CEmtYczVSE53cGJ0przEy-WZ546d3WrgoQh_wPmiIGo</recordid><startdate>1974</startdate><enddate>1974</enddate><creator>NAGANUMA, Mariko</creator><creator>FUKUSHIMA, Koji</creator><creator>TOYOSHIMA, Shigeshi</creator><general>The Japanese Pharmacological Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>1974</creationdate><title>Studies on the distribution of antitumor amino acid related compounds by whole body autoradiography in mice</title><author>NAGANUMA, Mariko ; FUKUSHIMA, Koji ; TOYOSHIMA, Shigeshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2839-d05f5b18d54f1dcd8ea9c810282f4c084d224366f1289a7f9c0531dc45eeef513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng ; jpn</language><creationdate>1974</creationdate><topic>AMINO ACIDS- TISSUE DISTRIBUTION</topic><topic>ANTINEOPLASTIC DRUGS- TISSUE DISTRIBUTION</topic><topic>AUTORADIOGRAPHY- CARBON 14 COMPOUNDS</topic><topic>BILE</topic><topic>BLOOD</topic><topic>KIDNEYS</topic><topic>LIVER</topic><topic>LUNGS</topic><topic>METABOLISM</topic><topic>MICE</topic><topic>N48830 -Life Sciences-New Tracer Techniques-Other</topic><topic>TIME DEPENDENCE</topic><topic>UPTAKE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>NAGANUMA, Mariko</creatorcontrib><creatorcontrib>FUKUSHIMA, Koji</creatorcontrib><creatorcontrib>TOYOSHIMA, Shigeshi</creatorcontrib><creatorcontrib>Keio Univ., Tokyo (Japan). School of Medicine</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Folia Pharmacologica Japonica</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>NAGANUMA, Mariko</au><au>FUKUSHIMA, Koji</au><au>TOYOSHIMA, Shigeshi</au><aucorp>Keio Univ., Tokyo (Japan). School of Medicine</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on the distribution of antitumor amino acid related compounds by whole body autoradiography in mice</atitle><jtitle>Folia Pharmacologica Japonica</jtitle><date>1974</date><risdate>1974</risdate><volume>70</volume><issue>6</issue><spage>849</spage><epage>861</epage><pages>849-861</pages><issn>0015-5691</issn><eissn>1347-8397</eissn><abstract>Four novel antitumor amino acid related compounds were labeled with 14C and the distribution was studied in mice. *A-91 was excreted into the bile, and a high level of radioactivity in the blood was maintained throughout the 24 hr of experiment. A high radio-activity was seen in the liver, lung, kidney, urinary bladder, and tumor. *A-145 was rapidly distributed to each tissue from the blood, especially to the pancreas, salivary glands, gastrointestinal tract, tumor, and other growing and secreting tissue. *A-192 was excreted into the bile and a high level of radioactivity was seen in the blood. A high radioactivity was detected in the liver, lung, kidney, uterus, ovary, and tumor, followed by a reduction paralleled with a concentration in the blood. *A-192 was rapidly excreted into the urine and very little radioactivity was observed in almost all organs and tissues, except for the central nervous system. *Cyclophosphamide was also rapidly excreted into the urine and bile, but only slight activity was observed in most organs. *Tryptophan, *isoleucine, *valinethese three had the same distribution patterns, and were incorporated into the growing and secreting tissues, pancreas, salivary glands, gastrointestinal tract, tumor, etc.</abstract><cop>Japan</cop><pub>The Japanese Pharmacological Society</pub><doi>10.1254/fpj.70.849</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AMINO ACIDS- TISSUE DISTRIBUTION ANTINEOPLASTIC DRUGS- TISSUE DISTRIBUTION AUTORADIOGRAPHY- CARBON 14 COMPOUNDS BILE BLOOD KIDNEYS LIVER LUNGS METABOLISM MICE N48830 -Life Sciences-New Tracer Techniques-Other TIME DEPENDENCE UPTAKE |
title | Studies on the distribution of antitumor amino acid related compounds by whole body autoradiography in mice |
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