Characterization of human recombinant alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung cells using intracellular Ca super(2+) changes: evidence for cross-talk between recombinant alpha sub(2A)- and native alpha sub(1)-adrenoceptors
Human alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung (CHL) fibroblasts have been pharmacologically characterized by measuring intracellular calcium (Ca super(2+) sub(i)) changes using the Ca super(2+)-sensitive dye Fluo3-AM, in conjunction with a fluorometric imaging plate reader (FLI...
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Veröffentlicht in: | British journal of pharmacology 2000-04, Vol.129 (7), p.1339-1346 |
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description | Human alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung (CHL) fibroblasts have been pharmacologically characterized by measuring intracellular calcium (Ca super(2+) sub(i)) changes using the Ca super(2+)-sensitive dye Fluo3-AM, in conjunction with a fluorometric imaging plate reader (FLIPR). Several alpha -adrenoceptor agonists were examined including the alpha sub(2)-adrenoceptor agonists UK-14304, B-HT 920, dexmedetomidine and A-54741, the selective alpha sub(1)-adrenoceptor agonist phenylephrine and the non-selective adrenergic agonist noradrenaline. Of these only noradrenaline (mean pEC sub(50) = 6.49) and A-54741 (6.90) evoked changes in Ca super(2+) sub(i); A-54741 was a partial agonist relative to noradrenaline, achieving only 33% of the noradrenaline maximum. Ca super(2+) sub(i) changes induced by noradrenaline and A-54741 were antagonized by the alpha sub(2)-selective antagonist rauwolscine (10 nM) and by the alpha sub(1)-selective antagonists prazosin (0.1 nM) and doxazosin (1.0 nM). Phenylephrine (100 mu M) and UK-14304 (10 mu M) alone were ineffective in causing Ca super(2+) sub(i) increase. In the presence of a fixed concentration of UK-14304 (3.0 mu M), phenylephrine induced concentration-dependent increases in Ca super(2+) sub(i) (mean pEC sub(50) = 5.33). In the presence of phenylephrine (30.0 mu M) UK-14304 induced Ca super(2+) sub(i) release (pEC sub(50) = 6.92). The effects of phenylephrine were abolished by prazosin (1.0 nM) or rauwolscine (100 nM). In saturation radioligand binding experiments using membranes of parental (non-transfected) CHL cells there was a small, specific binding of [ super(3)H]-prazosin (B sub(max) = 24 fmol mg protein super(-1); pK sub(D) = 10.24). Collectively, these data suggest that alpha -adrenoceptor agonist-induced Ca super(2+) sub(i) release in CHL fibroblasts transfected with the human alpha sub(2A)-adrenoceptor is dependent upon co-activation of the recombinant receptor and a native alpha sub(1)-adrenoceptor. |
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Several alpha -adrenoceptor agonists were examined including the alpha sub(2)-adrenoceptor agonists UK-14304, B-HT 920, dexmedetomidine and A-54741, the selective alpha sub(1)-adrenoceptor agonist phenylephrine and the non-selective adrenergic agonist noradrenaline. Of these only noradrenaline (mean pEC sub(50) = 6.49) and A-54741 (6.90) evoked changes in Ca super(2+) sub(i); A-54741 was a partial agonist relative to noradrenaline, achieving only 33% of the noradrenaline maximum. Ca super(2+) sub(i) changes induced by noradrenaline and A-54741 were antagonized by the alpha sub(2)-selective antagonist rauwolscine (10 nM) and by the alpha sub(1)-selective antagonists prazosin (0.1 nM) and doxazosin (1.0 nM). Phenylephrine (100 mu M) and UK-14304 (10 mu M) alone were ineffective in causing Ca super(2+) sub(i) increase. In the presence of a fixed concentration of UK-14304 (3.0 mu M), phenylephrine induced concentration-dependent increases in Ca super(2+) sub(i) (mean pEC sub(50) = 5.33). In the presence of phenylephrine (30.0 mu M) UK-14304 induced Ca super(2+) sub(i) release (pEC sub(50) = 6.92). The effects of phenylephrine were abolished by prazosin (1.0 nM) or rauwolscine (100 nM). In saturation radioligand binding experiments using membranes of parental (non-transfected) CHL cells there was a small, specific binding of [ super(3)H]-prazosin (B sub(max) = 24 fmol mg protein super(-1); pK sub(D) = 10.24). Collectively, these data suggest that alpha -adrenoceptor agonist-induced Ca super(2+) sub(i) release in CHL fibroblasts transfected with the human alpha sub(2A)-adrenoceptor is dependent upon co-activation of the recombinant receptor and a native alpha sub(1)-adrenoceptor.</description><identifier>ISSN: 0007-1188</identifier><language>eng</language><ispartof>British journal of pharmacology, 2000-04, Vol.129 (7), p.1339-1346</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Reynen, PH</creatorcontrib><creatorcontrib>Martin, G R</creatorcontrib><creatorcontrib>Eglen, R M</creatorcontrib><creatorcontrib>MacLennan, S J</creatorcontrib><title>Characterization of human recombinant alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung cells using intracellular Ca super(2+) changes: evidence for cross-talk between recombinant alpha sub(2A)- and native alpha sub(1)-adrenoceptors</title><title>British journal of pharmacology</title><description>Human alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung (CHL) fibroblasts have been pharmacologically characterized by measuring intracellular calcium (Ca super(2+) sub(i)) changes using the Ca super(2+)-sensitive dye Fluo3-AM, in conjunction with a fluorometric imaging plate reader (FLIPR). Several alpha -adrenoceptor agonists were examined including the alpha sub(2)-adrenoceptor agonists UK-14304, B-HT 920, dexmedetomidine and A-54741, the selective alpha sub(1)-adrenoceptor agonist phenylephrine and the non-selective adrenergic agonist noradrenaline. Of these only noradrenaline (mean pEC sub(50) = 6.49) and A-54741 (6.90) evoked changes in Ca super(2+) sub(i); A-54741 was a partial agonist relative to noradrenaline, achieving only 33% of the noradrenaline maximum. Ca super(2+) sub(i) changes induced by noradrenaline and A-54741 were antagonized by the alpha sub(2)-selective antagonist rauwolscine (10 nM) and by the alpha sub(1)-selective antagonists prazosin (0.1 nM) and doxazosin (1.0 nM). Phenylephrine (100 mu M) and UK-14304 (10 mu M) alone were ineffective in causing Ca super(2+) sub(i) increase. In the presence of a fixed concentration of UK-14304 (3.0 mu M), phenylephrine induced concentration-dependent increases in Ca super(2+) sub(i) (mean pEC sub(50) = 5.33). In the presence of phenylephrine (30.0 mu M) UK-14304 induced Ca super(2+) sub(i) release (pEC sub(50) = 6.92). The effects of phenylephrine were abolished by prazosin (1.0 nM) or rauwolscine (100 nM). In saturation radioligand binding experiments using membranes of parental (non-transfected) CHL cells there was a small, specific binding of [ super(3)H]-prazosin (B sub(max) = 24 fmol mg protein super(-1); pK sub(D) = 10.24). Collectively, these data suggest that alpha -adrenoceptor agonist-induced Ca super(2+) sub(i) release in CHL fibroblasts transfected with the human alpha sub(2A)-adrenoceptor is dependent upon co-activation of the recombinant receptor and a native alpha sub(1)-adrenoceptor.</description><issn>0007-1188</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNqNj01OwzAQhbMAifJzh1mhViiSU2gT2KEIxAG6rybOpDY4Y-OxC-LcHIBUYoFYIFZvNG_05ntHxUwpVZdV1TQnxanIs1LVTV2vZsVnazCiThTtBybrGfwAJo_IEEn7sbOMnABdMAiSu_nyflFiH4m9ppB8FKD3EEmEerAMrbFMQmBwlCkUXOYdaHJOIIudZstp-jctssMI7SE0UJwvrxagDfKO5A5ob3tiTTD4CDp6kTKhe4GO0hvRX2SA3ANPRfb0w6l-IZ8XxwM6oYtvPSsuHx827VMZon_NJGk7WjkwIpPPsq3q9ep23ajrfx9-Aa_dfXs</recordid><startdate>20000401</startdate><enddate>20000401</enddate><creator>Reynen, PH</creator><creator>Martin, G R</creator><creator>Eglen, R M</creator><creator>MacLennan, S J</creator><scope>7QP</scope></search><sort><creationdate>20000401</creationdate><title>Characterization of human recombinant alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung cells using intracellular Ca super(2+) changes: evidence for cross-talk between recombinant alpha sub(2A)- and native alpha sub(1)-adrenoceptors</title><author>Reynen, PH ; Martin, G R ; Eglen, R M ; MacLennan, S J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_176596803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reynen, PH</creatorcontrib><creatorcontrib>Martin, G R</creatorcontrib><creatorcontrib>Eglen, R M</creatorcontrib><creatorcontrib>MacLennan, S J</creatorcontrib><collection>Calcium & Calcified Tissue Abstracts</collection><jtitle>British journal of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reynen, PH</au><au>Martin, G R</au><au>Eglen, R M</au><au>MacLennan, S J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of human recombinant alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung cells using intracellular Ca super(2+) changes: evidence for cross-talk between recombinant alpha sub(2A)- and native alpha sub(1)-adrenoceptors</atitle><jtitle>British journal of pharmacology</jtitle><date>2000-04-01</date><risdate>2000</risdate><volume>129</volume><issue>7</issue><spage>1339</spage><epage>1346</epage><pages>1339-1346</pages><issn>0007-1188</issn><abstract>Human alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung (CHL) fibroblasts have been pharmacologically characterized by measuring intracellular calcium (Ca super(2+) sub(i)) changes using the Ca super(2+)-sensitive dye Fluo3-AM, in conjunction with a fluorometric imaging plate reader (FLIPR). Several alpha -adrenoceptor agonists were examined including the alpha sub(2)-adrenoceptor agonists UK-14304, B-HT 920, dexmedetomidine and A-54741, the selective alpha sub(1)-adrenoceptor agonist phenylephrine and the non-selective adrenergic agonist noradrenaline. Of these only noradrenaline (mean pEC sub(50) = 6.49) and A-54741 (6.90) evoked changes in Ca super(2+) sub(i); A-54741 was a partial agonist relative to noradrenaline, achieving only 33% of the noradrenaline maximum. Ca super(2+) sub(i) changes induced by noradrenaline and A-54741 were antagonized by the alpha sub(2)-selective antagonist rauwolscine (10 nM) and by the alpha sub(1)-selective antagonists prazosin (0.1 nM) and doxazosin (1.0 nM). Phenylephrine (100 mu M) and UK-14304 (10 mu M) alone were ineffective in causing Ca super(2+) sub(i) increase. In the presence of a fixed concentration of UK-14304 (3.0 mu M), phenylephrine induced concentration-dependent increases in Ca super(2+) sub(i) (mean pEC sub(50) = 5.33). In the presence of phenylephrine (30.0 mu M) UK-14304 induced Ca super(2+) sub(i) release (pEC sub(50) = 6.92). The effects of phenylephrine were abolished by prazosin (1.0 nM) or rauwolscine (100 nM). In saturation radioligand binding experiments using membranes of parental (non-transfected) CHL cells there was a small, specific binding of [ super(3)H]-prazosin (B sub(max) = 24 fmol mg protein super(-1); pK sub(D) = 10.24). Collectively, these data suggest that alpha -adrenoceptor agonist-induced Ca super(2+) sub(i) release in CHL fibroblasts transfected with the human alpha sub(2A)-adrenoceptor is dependent upon co-activation of the recombinant receptor and a native alpha sub(1)-adrenoceptor.</abstract></addata></record> |
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title | Characterization of human recombinant alpha sub(2A)-adrenoceptors expressed in Chinese hamster lung cells using intracellular Ca super(2+) changes: evidence for cross-talk between recombinant alpha sub(2A)- and native alpha sub(1)-adrenoceptors |
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