Comparative biochemistry and physiology. C: Comparative pharmacology最新文献

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Alteration of starfish oocyte adenylate cyclase properties in gametogenesis 海星卵母细胞腺苷酸环化酶特性在配子体发生中的改变
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-07-01 DOI: 10.1016/0742-8413(93)90097-5
N.E. Lamash, E.M. Karaseva, Yu S. Khotimchenko
{"title":"Alteration of starfish oocyte adenylate cyclase properties in gametogenesis","authors":"N.E. Lamash,&nbsp;E.M. Karaseva,&nbsp;Yu S. Khotimchenko","doi":"10.1016/0742-8413(93)90097-5","DOIUrl":"10.1016/0742-8413(93)90097-5","url":null,"abstract":"<div><p>1. The properties of the oocyte membrane adenylate cyclase system of the starfish <em>Aphelasterias japonica</em> at different stages of gametogenesis were studied.</p><p>2. The adenylate cyclase activity of fully grown oocytes was insensitive to catecholamines whereas activity in growing oocytes was increased.</p><p>3. Forskolin and NaF stimulated catalytic activity of growth and fully grown oocytes to various degrees. The stimulated effect of these modifiers was more considerable in grown oocytes.</p><p>4. We believe that the interaction between components of the adenylate cyclase system is altered in gametogenesis.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 3","pages":"Pages 531-534"},"PeriodicalIF":0.0,"publicationDate":"1993-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90097-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"54006555","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Effect of cypermethrin on the free amino acids pool in an organophosphorus-insecticide-resistant and a susceptible strain of Tribolium castaneum 氯氰菊酯对一株抗有机磷杀虫剂和一株敏感虫游离氨基酸池的影响
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-07-01 DOI: 10.1016/0742-8413(93)90100-Y
Mushtaq A. Saleem, A.R. Shakoori
{"title":"Effect of cypermethrin on the free amino acids pool in an organophosphorus-insecticide-resistant and a susceptible strain of Tribolium castaneum","authors":"Mushtaq A. Saleem,&nbsp;A.R. Shakoori","doi":"10.1016/0742-8413(93)90100-Y","DOIUrl":"10.1016/0742-8413(93)90100-Y","url":null,"abstract":"<div><p>1. Proline was found to be the major component of CTC-12 (44%) and FSS II (45%) strain.</p><p>2. The cypermethrin treatment resulted in an increase in most of the amino acids of sixth instar larvae and all amino acids of adult beetles of CTC 12 strain.</p><p>3. In the susceptible strain (FSS II), however, the tyrosine, phenylalanine and arginine increased, whereas serine, proline, glycine, alanine, valine, isoleucine, leucine and lysine were decreased significantly in the sixth instar larvae.</p><p>4. In the FSS II adult beetles, only aspartic acid increased, while other amino acids either decreased (threonine, proline, glycine, alanine, valine, methionine, isoleucine, tyrososine, lysine, arginine) or remained unaffected (serine, glutamic acid, leucine, phenylalanine, histidine).</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 3","pages":"Pages 549-553"},"PeriodicalIF":0.0,"publicationDate":"1993-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90100-Y","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"54006579","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 12
Role of GABA in hypoxia tolerance, metabolic depression and hibernation—Possible links to neurotransmitter evolution GABA在缺氧耐受、代谢抑制和冬眠中的作用——可能与神经递质进化有关
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-07-01 DOI: 10.1016/0742-8413(93)90069-W
G.E. Nilsson , P.L. Lutz
{"title":"Role of GABA in hypoxia tolerance, metabolic depression and hibernation—Possible links to neurotransmitter evolution","authors":"G.E. Nilsson ,&nbsp;P.L. Lutz","doi":"10.1016/0742-8413(93)90069-W","DOIUrl":"10.1016/0742-8413(93)90069-W","url":null,"abstract":"<div><p>1. The roles of the inhibitory neurotransmitter GABA and the excitatory neurotransmitter glutamate in anoxic survival and anoxic death are discussed, with particular reference to the brain.</p><p>2. It is pointed out that the metabolic relationship between GABA and glutamate causes the neural levels of GABA to increase and glutamate to decrease during anoxia.</p><p>3. It is suggested that increased levels of GABA could mediate metabolic depression, and, thus, anoxic survival in ectothennic as well as endothermic vertebrates. Furthermore, evidence for a role of GABA in hibernation is discussed.</p><p>4. A hypothesis is presented suggesting that hypoxia has been a selective pressure in conserving GABA and glutamate as major inhibitory and excitatory neurotransmitters in vertebrates as well as invertebrates.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 3","pages":"Pages 329-336"},"PeriodicalIF":0.0,"publicationDate":"1993-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90069-W","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"18897027","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 62
Toxic effects of mercury on the hard clam, Meretrix lusoria, in various salinities 汞在不同盐度下对硬蛤的毒性作用
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-07-01 DOI: 10.1016/0742-8413(93)90092-Y
Tzong-Shean Chin, Hon-Cheng Chen
{"title":"Toxic effects of mercury on the hard clam, Meretrix lusoria, in various salinities","authors":"Tzong-Shean Chin,&nbsp;Hon-Cheng Chen","doi":"10.1016/0742-8413(93)90092-Y","DOIUrl":"10.1016/0742-8413(93)90092-Y","url":null,"abstract":"<div><p>1. The 96-hr <span>lc</span><sub>50</sub> values for juvenile hard clams, <em>Meretrix lusoria</em>, were 328, 392 and 194 μg/l Hg in 10, 20 and 30 ppt salinities at 25 ± 1°C, respectively; for adult hard clams 341 and 140 μg/l Hg in 20 and 30 ppt salinities, respectively.</p><p>2. Acclimatizing the adult clams to low salinity of 10 ppt lessened the toxicity of mercury. However, juvenile animals appeared to be more sensitive to mercury poisoning after 96 hr exposure in 10 ppt salinity.</p><p>3. All embryos exposed to 40 μg/l Hg and above died within 30 hr. In the control, 44% of hatched embryos had developed into D-stage larvae, while those exposed to 20 μg/l Hg were still in the trochophore stage. Most of the retarded larvae developed into abnormal forms within 30 hr at 28°C in 15 ppt salinity.</p><p>4. In order to maintain water quality and protect natural resources, the recommended safe level of mercury is 0.046 (0.039–0.053) μg/l Hg, based on the estimated 30-hr <span>EC</span><sub>50</sub> for the clam embryos, with an application factor of 0.01.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 3","pages":"Pages 501-507"},"PeriodicalIF":0.0,"publicationDate":"1993-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90092-Y","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"54006522","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
Cellular damage in the rat heart caused by caffeine or dinitrophenol 咖啡因或二硝基酚引起的大鼠心脏细胞损伤
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90199-U
Stephanie Daniels, C.J. Duncan
{"title":"Cellular damage in the rat heart caused by caffeine or dinitrophenol","authors":"Stephanie Daniels,&nbsp;C.J. Duncan","doi":"10.1016/0742-8413(93)90199-U","DOIUrl":"10.1016/0742-8413(93)90199-U","url":null,"abstract":"<div><p>1. Langendorff-perfusion of rat hearts with either 10 mM caffeine or 1 mM 2,4-dinitrophenol (DNP) caused severe ultrastructural damage to the myofilaments and mitochondria that was similar to that found in a standard Ca<sup>2+</sup>-paradox.</p><p>2. This damage occurred in the presence and absence of extracellular Ca<sup>2+</sup></p><p>3. Creatine kinase (CK) release (indicative of sarcolemma breakdown) was not recorded unless the caffeine- or DNP-perfusion was preceded by Ca<sup>2+</sup><sub>0</sub>-depletion.</p><p>4. It is concluded that: (i) the pathways leading to damage to the myofilaments and sarcolemma are independent; (ii) the CK release mechanism requires dual activation of Ca<sup>2+</sup><sub>0</sub>-depletion plus a rise in [Ca<sup>2+</sup>]<sub>i</sub>; and (iii) current theories concerning the mechanisms underlying the genesis of the Ca<sup>2+</sup>-paradox are incorrect or incomplete.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 225-229"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90199-U","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19096847","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Toxicity of tetrachlorwinfos to Rana temporaria l. 四氯窗氟醚对天蚕的毒性研究。
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90209-4
K. Gromysz-Kałkowska, E. Szubartowska
{"title":"Toxicity of tetrachlorwinfos to Rana temporaria l.","authors":"K. Gromysz-Kałkowska,&nbsp;E. Szubartowska","doi":"10.1016/0742-8413(93)90209-4","DOIUrl":"10.1016/0742-8413(93)90209-4","url":null,"abstract":"<div><p>1. Changes in the erythrocyte system of frogs poisoned with tetrachlorwinfos depend on the sex of the animals and the dose of pesticide applied. They are a result of the pathomorphological changes due to translocation of fluids from the tissues to the circulation and swelling of the blood cells.</p><p>2. Changes in the leucocyte system of frogs are caused by several mechanisms: lytic action of the pesticide on the blood cell membrane, the stressogenic effect of the agent and enhanced activity of the reticuloendothelial system.</p><p>3. The appearance of typical changes due to stress, after even the lowest dose of tetrachlorwinfos, and low <span>ld</span><sub>50</sub> values indicate that this pesticide is highly toxic for frogs.</p><p>4. The relatively high susceptibility of frogs to intoxication with tetrachlorwinfos is probably the result of a high affinity of cholinesterase to this pesticide, because of the presence of the <em>P</em>=<em>O</em> bond in its molecule.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 285-290"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90209-4","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19096852","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Presynaptic block of transmission in the insect CNS by mono- and di-galactosyl analogues of vespulakinin 1, a wasp (Paravespula maculifrons) venom neurotoxin 黄蜂毒液神经毒素vespulakinin 1的单半乳糖和双半乳糖类似物在昆虫中枢神经系统中的突触前传导阻滞
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90193-O
T. Piek , B. Hue , H. Le Corronc , P. Mantel , M. Gobbo , R. Rocchi
{"title":"Presynaptic block of transmission in the insect CNS by mono- and di-galactosyl analogues of vespulakinin 1, a wasp (Paravespula maculifrons) venom neurotoxin","authors":"T. Piek ,&nbsp;B. Hue ,&nbsp;H. Le Corronc ,&nbsp;P. Mantel ,&nbsp;M. Gobbo ,&nbsp;R. Rocchi","doi":"10.1016/0742-8413(93)90193-O","DOIUrl":"10.1016/0742-8413(93)90193-O","url":null,"abstract":"<div><p>1. The pharmacological properties of four synthetic analogues of the wasp neurotoxin, Vespulakinin 1, were studied using a cascade of mammalian smooth muscle preparations and the synaptic transmission from the cockroach cereal nerves to a giant interneuron.</p><p>2. All analogues have an extremely slow bradykinin-like effect on the smooth muscles. The carbohydrate-free and the two mono-glycosylated analogues are about equally active with bradykinin.</p><p>3. The double glycosylated derivative is about 5 times more potent than bradykinin.</p><p>4. All analogues have two different effects on synaptic transmission in the insect CNS—at first a direct and reversible block of excitatory nicotinic transmission with a concurrent activation of the inhibitory GABA-ergic system and, secondly, a delayed irreversible block of the transmission, comparable to the block described earlier for bradykinin and Thr<sup>6</sup>-bradykinin.</p><p>5. For the synaptic transmission in the insect CNS the double glycosylated kinin is about 5 times more potent than bradykinin.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 189-196"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90193-O","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19096863","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 15
The action of four proposed chloride movement modifiers on acetylcholine responses of central neurones of Helix aspersa 四种氯离子运动调节剂对螺旋树中枢神经元乙酰胆碱反应的影响
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90213-5
N.J.D. Wright , R.J. Walker
{"title":"The action of four proposed chloride movement modifiers on acetylcholine responses of central neurones of Helix aspersa","authors":"N.J.D. Wright ,&nbsp;R.J. Walker","doi":"10.1016/0742-8413(93)90213-5","DOIUrl":"https://doi.org/10.1016/0742-8413(93)90213-5","url":null,"abstract":"<div><p>1. Intracellular recordings were made from identified neurones in the visceral, (abdominal) ganglion of the snail, <em>Helix aspersa</em>. The hyperpolarising response of neurone E4 is a pure chloride event and has a reversal potential, (<em>E</em><sub>Cl</sub>), of −69.7 ± 1.7mV, (<em>n</em> = 4). This can be compared to depolarising responses of neurones E1 and E2 which are sodium mediated.</p><p>2. Four membrane transport system antagonists, all thought to affect trans-membrane chloride movement, were investigated with respect to the two different acetylcholine responses described.</p><p>3. Piretanide irreversibly blocks the hyperpolarising response in cell E4, (1–10 μM), increasing its inhibition with time but without changing <em>E</em><sub>Cl</sub>.</p><p>4. Furosemide irreversibly blocks both types of acetylcholine responses at concentrations in the nanomolar range; no change in <em>E</em><sub>Cl</sub> or <em>E</em><sub>Na</sub> was associated with the inhibition but the “passive” membrane resistance appeared to decrease. Inhibition increased with time, normally causing a significant effect after 10–30 min.</p><p>5. S.I.T.S. and ethacrynic acid appear very similar in effect; both reversibly block the two responses to acetylcholine and recovery after washing is virtually complete. The onset of antagonism is rapid and both compounds are slightly more effective against the hyperpolarising (“H”), response than the depolarising (“D”) response (threshold ∼10<sup>−5</sup> M compared to ∼ 10<sup>−4</sup> M). No change in <em>E</em><sub>Cl</sub> or <em>E</em><sub>Na</sub> was noted.</p><p>6. Piretanide and furosemide probably exert their effect by interactions with the neuronal cell membrane, disrupting the integrity of this structure, whereas S.I.T.S. and ethacrynic acid may interact more specifically with the acetylcholine receptor protein.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 311-322"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90213-5","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136596942","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Cadmium induced metallothionein in hepatopancreas of Procambarus clarkii: Quantification by a silver-saturation method 克氏原螯虾肝胰脏中镉诱导的金属硫蛋白:用饱和银法定量
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90205-Y
Manuela Martínez , Amparo Torreblanca , Jose Del Ramo , Agustín Pastor , Javier Díaz-Mayans
{"title":"Cadmium induced metallothionein in hepatopancreas of Procambarus clarkii: Quantification by a silver-saturation method","authors":"Manuela Martínez ,&nbsp;Amparo Torreblanca ,&nbsp;Jose Del Ramo ,&nbsp;Agustín Pastor ,&nbsp;Javier Díaz-Mayans","doi":"10.1016/0742-8413(93)90205-Y","DOIUrl":"https://doi.org/10.1016/0742-8413(93)90205-Y","url":null,"abstract":"<div><p>1. Cadmium induced metallothionein (MT) in crayfish hepatopancreas was measured by silver-saturation method.</p><p>2. An increase in MT content was recorded in crayfish hepatopancreas after 12 hr of exposure to 10 mg Cd/l.</p><p>3. There was found to be a linear relationship between MT concentrations in hepatopancreas and cadmium concentration in the water.</p><p>4. MT levels in hepatopancreas of 20 mg Cd/l exposed crayfish were 7-fold higher than those in control animals.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 263-267"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90205-Y","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136597558","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 34
Arachidonic acid, protein kinase C activators and bud formation in Hydra vulgaris 花生四烯酸、蛋白激酶C激活剂与水螅芽形成
Comparative biochemistry and physiology. C: Comparative pharmacology Pub Date : 1993-06-01 DOI: 10.1016/0742-8413(93)90198-T
Luciano De Petrocellis , Vincenzo Di Marzo , Carmen Gianfrani , Rosario Minei
{"title":"Arachidonic acid, protein kinase C activators and bud formation in Hydra vulgaris","authors":"Luciano De Petrocellis ,&nbsp;Vincenzo Di Marzo ,&nbsp;Carmen Gianfrani ,&nbsp;Rosario Minei","doi":"10.1016/0742-8413(93)90198-T","DOIUrl":"https://doi.org/10.1016/0742-8413(93)90198-T","url":null,"abstract":"<div><p>1. The effect of the protein kinase C (PKC) activators verrucosin B (VB), 1,2-sn-dioctanoylglycerol (diC<sub>8</sub>) and phorbol-12-myristate-13-acetate (PMA), of arachidonic acid (AA) and of substances interfering with its release, re-uptake and metabolism was studied in <em>Hydra vulgaris</em>.</p><p>2. All PKC activators potently inhibited bud formation, VB and PMA being 10,000 × more potent than diC<sup>8</sup>. VB effect was maximal already after 10 min incubation with hydra and persisted at 24 hr incubations.</p><p>3. AA and substances inhibiting its re-uptake from cell membrane or its metabolism also inhibited bud formation, whereas oleyl-oxyethyl-phosphorylcholine (OOPC), an inhibitor of phospholipase A<sub>2</sub>, potently induced bud formation.</p><p>4. The findings described herein suggest a role for both PKC activation and AA in the inhibition of bud formation in <em>H. vulgaris</em>.</p></div>","PeriodicalId":72650,"journal":{"name":"Comparative biochemistry and physiology. C: Comparative pharmacology","volume":"105 2","pages":"Pages 219-224"},"PeriodicalIF":0.0,"publicationDate":"1993-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/0742-8413(93)90198-T","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136597561","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
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